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Beyond weight loss: a review of the therapeutic uses of very-low-carbohydrate (ketogenic) diets.
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PMID:  23801097     Owner:  NLM     Status:  MEDLINE    
Very-low-carbohydrate diets or ketogenic diets have been in use since the 1920s as a therapy for epilepsy and can, in some cases, completely remove the need for medication. From the 1960s onwards they have become widely known as one of the most common methods for obesity treatment. Recent work over the last decade or so has provided evidence of the therapeutic potential of ketogenic diets in many pathological conditions, such as diabetes, polycystic ovary syndrome, acne, neurological diseases, cancer and the amelioration of respiratory and cardiovascular disease risk factors. The possibility that modifying food intake can be useful for reducing or eliminating pharmaceutical methods of treatment, which are often lifelong with significant side effects, calls for serious investigation. This review revisits the meaning of physiological ketosis in the light of this evidence and considers possible mechanisms for the therapeutic actions of the ketogenic diet on different diseases. The present review also questions whether there are still some preconceived ideas about ketogenic diets, which may be presenting unnecessary barriers to their use as therapeutic tools in the physician's hand.
A Paoli; A Rubini; J S Volek; K A Grimaldi
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Publication Detail:
Type:  Journal Article; Review     Date:  2013-06-26
Journal Detail:
Title:  European journal of clinical nutrition     Volume:  67     ISSN:  1476-5640     ISO Abbreviation:  Eur J Clin Nutr     Publication Date:  2013 Aug 
Date Detail:
Created Date:  2013-08-07     Completed Date:  2014-02-20     Revised Date:  2014-06-11    
Medline Journal Info:
Nlm Unique ID:  8804070     Medline TA:  Eur J Clin Nutr     Country:  England    
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Languages:  eng     Pagination:  789-96     Citation Subset:  IM    
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MeSH Terms
Cardiovascular Diseases / diet therapy,  metabolism
Diet, Carbohydrate-Restricted*
Diet, Reducing
Dietary Carbohydrates / administration & dosage
Glucose / metabolism
Ketogenic Diet*
Metabolic Diseases / diet therapy*,  metabolism
Neoplasms / diet therapy*
Nervous System Diseases / diet therapy*,  metabolism
Obesity / diet therapy,  metabolism
Weight Loss / physiology*
Reg. No./Substance:
0/Dietary Carbohydrates; IY9XDZ35W2/Glucose
Erratum In:
Eur J Clin Nutr. 2014 May;68(5):641

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

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Journal Information
Journal ID (nlm-ta): Eur J Clin Nutr
Journal ID (iso-abbrev): Eur J Clin Nutr
ISSN: 0954-3007
ISSN: 1476-5640
Publisher: Nature Publishing Group
Article Information
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Copyright © 2013 Macmillan Publishers Limited
Received Day: 20 Month: 01 Year: 2013
Revision Received Day: 27 Month: 05 Year: 2013
Accepted Day: 29 Month: 05 Year: 2013
Print publication date: Month: 08 Year: 2013
Electronic publication date: Day: 26 Month: 06 Year: 2013
Volume: 67 Issue: 8
First Page: 789 Last Page: 796
PubMed Id: 23801097
ID: 3826507
Publisher Item Identifier: ejcn2013116
DOI: 10.1038/ejcn.2013.116

Beyond weight loss: a review of the therapeutic uses of very-low-carbohydrate (ketogenic) diets Alternate Title:Therapeutic uses of ketogenic diets
A Paoli1*
A Rubini1
J S Volek2
K A Grimaldi3
1The Physiological Laboratory, Department of Biomedical Sciences, University of Padova, Padova, Italy
2Human Performance Laboratory, Department of Kinesiology, University of Connecticut, Storrs, CT, USA
3Biomedical Engineering Laboratory, Institute of Communication and Computer Systems, National Technical University of Athens, Athens, Greece
*The Physiological Laboratory, Department of Biomedical Sciences, University of Padova, via Marzolo 3, Padova 35131, Italy. E-mail:


During recent years, an increasing amount of evidence has accumulated in the literature, suggesting that very-low-carbohydrate ketogenic diets (VLCKD) could have a therapeutic role in numerous diseases. The use of VLCKD in treating epilepsy has been well established for many decades and these diets have become even more widely known, as they became popular in the 1970s for weight loss—especially as the ‘Atkins Diet'.1 More recently, the therapeutic use of ketogenic diets in other diseases has been studied with positive results—it is an important direction for research because, clearly, if nutritional intervention can reduce reliance on pharmaceutical treatments it would bring significant benefits from an economic as well as a social point of view given the current US $750 billion annual cost of pharmaceuticals.2

Ketogenic diets are characterized by a reduction in carbohydrates (usually to less than 50 g/day) and a relative increase in the proportions of protein and fat.3 The knowledge regarding the metabolic effects of classic ketogenic diets originates from the pioneering work of Cahill and colleagues in the 1960s,4 but the realization of the importance of these diets from a clinical point of view can be traced back to the early 1920s when they began to be successfully used in the treatment of epilepsy.5 There even appears to be a reference to its use in the Bible in the story of the cured epileptic (New Testament, Matthew 17:14–21). Alongside the huge amount of data about the influence of correct nutrition on health status and disease prevention (encapsulated in various nutritional guidelines delivered by public health committees worldwide), there is also ample evidence to support the notion that a low-carbohydrate diet can lead to an improvement in some metabolic pathways and have beneficial health effects. To use ‘food as medicine' is as attractive a concept as it is ancient, and in the hope of realizing this much effort has been dedicated to exploring the effects of VLCKD on human metabolism. In this review we will look at all the areas where ketogenic diets have been proposed as having potential clinical utility with a brief discussion of the evidence.

What is ketosis?

Insulin activates key enzymes in pathways, which store energy derived from carbohydrates, and when there is an absence or scarcity of dietary carbohydrates the resulting reduced insulin level leads to a reduction in lipogenesis and fat accumulation. After a few days of fasting, or of drastically reduced carbohydrate consumption (below 50 g/day), glucose reserves become insufficient both for normal fat oxidation via the supply of oxaloacetate in the Krebs cycle (which gave origin to the phrase ‘fat burns in the flame of carbohydrate') and for the supply of glucose to the central nervous system (CNS).4

The CNS cannot use fat as an energy source; hence, it normally utilizes glucose. After 3–4 days without carbohydrate consumption the CNS is ‘forced' to find alternative energy sources, and as demonstrated by the classic experiments of Cahill and colleagues4 this alternative energy source is derived from the overproduction of acetyl coenzyme A (CoA). This condition seen in prolonged fasting, type 1 diabetes and high-fat/low-carbohydrate diets leads to the production of higher-than-normal levels of so-called ketone bodies (KBs), that is, acetoacetate, β-hydroxybutyric acid and acetone—a process called ketogenesis and which occurs principally in the mitochondrial matrix in the liver.6

The main KB produced in the liver is acetoacetate but the primary circulating ketone is β-hydroxybutyrate although the latter is not, strictly speaking, a KB because the ketone moiety has been reduced to a hydroxyl group. Under normal conditions of adequate dietary carbohydrate, the production of free acetoacetic acid is negligible and it is rapidly metabolized by various tissues, especially the skeletal and heart muscles. In conditions of overproduction of acetoacetic acid, it accumulates above normal levels and part of it is converted to the other two KBs leading to ketonemia and ketonuria (presence of KBs in the blood and urine). The characteristic ‘sweet' breath odour of ketosis is caused by acetone, which, being a very volatile compound, is eliminated mainly via respiration in the lungs. The pathway that results in the formation of 3-hydroxy-3-methylglutaryl–CoA from acetyl CoA also occurs in the cytosol of hepatic cells where it is used instead for the biosynthesis of cholesterol. Under normal conditions, the concentration of KBs is very low (<0.3 mmol/l) compared with glucose (∼4 mmol), and as glucose and KBs have a similar kM for glucose transport to the brain the KBs begin to be utilized as an energy source by the CNS when they reach a concentration of about 4 mmol/l, which is close to the Km for the monocarboxylate transporter.3, 6

KBs are then used by tissues as a source of energy3 through a pathway that leads to formation from β-hydroxybutyrate of two molecules of acetyl CoA, which are used finally in the Krebs cycle. It is interesting to note that the KBs are able to produce more energy compared with glucose because of the metabolic effects of ketosis—the high chemical potential of 3-β-hydroxybutyrate leads to an increase in the ΔG0 of ATP hydrolysis.3 A further point to underline is, as shown in Table 1, that glycaemia, even though reduced, remains within physiological levels because of the fact that glucose is formed from two sources: from glucogenic amino acids and from glycerol liberated via lysis from triglycerides.7

We would like to emphasize that ketosis is a completely physiological mechanism and it was the biochemist Hans Krebs who first referred to physiological ketosis to differentiate it from the pathological keto acidosis seen in type 1 diabetes.8 In physiological ketosis (which occurs during very-low-calorie ketogenic diets), ketonemia reaches maximum levels of 7/8 mmol/l (it does not go higher precisely because the CNS efficiently uses these molecules for energy in place of glucose) and with no change in pH, whereas in uncontrolled diabetic ketoacidosis it can exceed 20 mmol/l with a concomitant lowering of blood pH9, 10 (Table 1).

Therapeutic roles of ketogenic diets
Strong evidence
Weight loss

There is no doubt that there is strong supportive evidence that the use of ketogenic diets in weight-loss therapy is effective; however, there are contrasting theories regarding the mechanisms through which they work. Some researchers suggest that there are not in fact any metabolic advantages in low-carbohydrate diets and that weight loss results simply from reduced caloric intake, probably due to the increased satiety effect of protein.12 Others instead promote the hypothesis that there is indeed a distinct metabolic advantage, which has recently been explored in more detail, raising interest in the role of VLCKD in weight loss and effects on metabolism in general.13 The first law of thermodynamics, also known as the law of conservation of energy, has in effect controlled the concepts for the basis of weight loss for over a century—resulting in a difficulty in accepting other ways of thinking. Adhering to these traditional concepts the US Department of Agriculture has concluded that diets, which reduce calories, will result in effective weight loss independent of the macronutrient composition, which is considered less important, even irrelevant.14 In contrast with these views, the majority of ad-libitum studies demonstrate that subjects who follow a low-carbohydrate diet lose more weight during the first 3–6 months compared with those who follow balanced diets.15, 16, 17 One hypothesis is that the use of energy from proteins in VLCKD is an ‘expensive' process for the body and so can lead to a ‘waste of calories', and therefore increased weight loss compared with other ‘less-expensive' diets.13, 18, 19 The average human body requires 60–65 g of glucose per day, and during the first phase of a diet very low in carbohydrates this is partially (16%) obtained from glycerol, with the major part derived via gluconeogenesis from proteins of either dietary or tissue origin.12 The energy cost of gluconeogenesis has been confirmed in several studies7 and it has been calculated at ∼400–600 Kcal/day (due to both endogenous and food source proteins.18 Despite this, there is no direct experimental evidence to support this intriguing hypothesis; on the contrary, a recent study reported that there were no changes in resting energy expenditure after a VLCKD.20 A simpler, perhaps more likely, explanation for improved weight loss is a possible appetite-suppressant action of ketosis. The mechanism for this is not established but evidence supports direct action of KBs together with modifications in levels of hormones, which influence appetite, such as ghrelin and leptin.21 Here we can summarize (listed in order of importance and available evidence) that the weight-loss effect of VLCKD seems to be caused by several factors:

  1. Reduction in appetite due to higher satiety effect of proteins,12, 22 effects on appetite control hormones21 and to a possible direct appetite-suppressant action of the KBs.23
  2. Reduction in lipogenesis and increased lipolysis.7, 10
  3. Reduction in the resting respiratory quotient and, therefore, greater metabolic efficiency in consuming fats.20, 24
  4. Increased metabolic costs of gluconeogenesis and the thermic effect of proteins.13, 18

Cardiovascular disease

Several lines of evidence point to beneficial effects of VLCKD on cardiovascular risk factors. In the past, there have been doubts expressed about their long-term safety and increased effectiveness compared with ‘balanced' diets,25 and clearly negative opinions regarding possible deleterious effects on triglycerides and cholesterol levels in the blood.26 However, the majority of recent studies seem instead to amply demonstrate that the reduction of carbohydrates to levels that induce physiological ketosis (see above ‘What is ketosis?' section) can actually lead to significant benefits in blood lipid profiles.15, 17, 27 The VLCKD effect seems to be particularly marked on the level of blood triglycerides,24, 28 but there are also significant positive effects on total cholesterol reduction and increases in high-density lipoprotein.24, 28, 29 Furthermore, VLCKD have been reported to increase the size and volume of low-density lipoprotein–cholesterol particles,29 which is considered to reduce cardiovascular disease risk, as smaller low-density lipoprotein particles have a higher atherogenicity. There are also direct diet-related effects on overall endogenous cholesterol synthesis. A key enzyme in cholesterol biosynthesis is 3-hydroxy-3-methylglutaryl–CoA reductase (the target for statins), which is activated by insulin, which means that an increase in blood glucose and consequently of insulin levels will lead to increased endogenous cholesterol synthesis. A reduction in dietary carbohydrate will have the opposite effect and this, coupled with the additional inhibition by dietary cholesterol and fats on endogenous synthesis, is likely to be the mechanism via which physiological ketosis can improve lipid profiles. Hence, there are strong doubts about the negative effects of dietary fats when they are consumed as part of a VLCKD, on cholesterol and triglycerides blood levels, whereas there are strong pointers to the beneficial effects of VLCKD on these cardiovascular risk parameters.27, 28

Type 2 diabetes

Insulin resistance is the primary feature underlying type 2 diabetes (T2D) but it also exists across a continuum in the general population, and to varying extents it disrupts insulin action in cells, which can cause a wide spectrum of signs and symptoms. A primary feature of insulin resistance is an impaired ability of muscle cells to take up circulating glucose. A person with insulin resistance will divert a greater proportion of dietary carbohydrate to the liver where much of it is converted to fat (that is, de novo lipogenesis), as opposed to being oxidized for energy in skeletal muscle.30 Although Hellerstein31 has recently reported that de novo lipogenesis contributes only ∼20% of new triglycerides, this greater conversion of dietary carbohydrate into fat, much of it entering the circulation as saturated fat, is a metabolic abnormality that significantly increases risk for diabetes and heart disease. Thus, insulin resistance functionally manifests itself as ‘carbohydrate intolerance'. When dietary carbohydrate is restricted to a level below which it is not significantly converted to fat (a threshold that varies from person to person), signs and symptoms of insulin resistance improve or often disappear completely.

In studies that have evaluated well-formulated very-low-carbohydrate diets and documented high rates of compliance in individuals with T2D, results have been nothing short of remarkable. Bistrian et al.32 reported withdrawal of insulin and major weight loss in a matter of weeks in T2D individuals who were fed a very-low-calorie and -carbohydrate diet. Gumbiner et al.33 fed obese T2D individuals two types of hypocaloric (650 kcal) diets for 3 weeks, they were matched for protein but one was much lower in carbohydrate content (24 vs 94 g/day). As expected, the lower-carbohydrate diet resulted in significantly greater levels of circulating ketones (∼3 mmol/l), which was strongly associated with a lower hepatic glucose output. Interestingly, there was a strong inverse correlation between circulating ketones and hepatic glucose output, suggesting that higher levels of ketones are associated with more favourable effects on glycaemic control in diabetics. More recently, Boden et al.34 performed an in-patient study in obese T2D individuals who were fed a low-carbohydrate (<20 g/day) diet for 2 weeks. Plasma glucose fell from 7.5 to 6.3 mmol/l, haemoglobin A1c decreased from 7.3 to 6.8% and there were dramatic improvements (75%) in insulin sensitivity.

In a longer study35 obese T2D individuals were prescribed a well-formulated ketogenic diet for 56 weeks, and significant improvements in both weight loss and metabolic parameters were seen at 12 weeks and continued throughout the 56 weeks as evidenced by improvements in fasting circulating levels of glucose (−51%), total cholesterol (−29%), high-density lipoprotein–cholesterol (63%), low-density lipoprotein–cholesterol (−33%) and triglycerides (−41%). It is of interest to note that in a recent study in overweight non/diabetic subjects, it was reported that during ketosis fasting glucose was not affected, but there was an elevation in post-prandial blood glucose concentration. This data suggests a different effect of ketosis on glucose homeostasis in diabetic and non-diabetic individuals.21 Other studies support the long-term efficacy of ketogenic diets in managing complications of T2D.36, 37 Although significant reductions in fat mass often results when individuals restrict carbohydrate, the improvements in glycaemic control, haemoglobin A1c and lipid markers, as well as reduced use or withdrawal of insulin and other medications in many cases, occurs before significant weight loss occurs. Moreover, in isocaloric experiments individuals with insulin resistance showed dramatically improved markers of metabolic syndrome than diets lower in fat.27 It is interesting in this respect that a recent extremely large epidemiological study reported that diabetes risk is directly correlated, in an apparently causative manner, with sugar intake alone, independently of weight or sedentary lifestyle.38

In summary, individuals with metabolic syndrome, insulin resistance and T2D (all diseases of carbohydrate intolerance) are likely to see symptomatic as well as objective improvements in biomarkers of disease risk if they follow a well-formulated very-low-carbohydrate diet. Glucose control improves not only because there is less glucose coming in, but also because systemic insulin sensitivity improves as well.


Since 1920, the ketogenic diet has been recognized as an effective tool in the treatment of severe childhood epilepsy, but following the introduction of anticonvulsant drugs, the interest in ketogenic diet treatment waned until the 1990s, with subsequent research and clinical trials demonstrating its practical usefulness. Various studies have been carried out to understand its mechanism of action in epilepsy, but until now it remains largely uncertain.5 Several hypotheses have been put forward trying to explain the mechanism of action of ketogenic diets: (1) a direct anticonvulsant effect of KBs; (2) a reduced neuronal excitability induced by KBs;39 (3) an effect on the mammalian target of rapamycin pathway.40 In 2008, Hartman et al.41 demonstrated the efficacy of a ketogenic diet in the 6-Hz seizure test in mice, but also reported that the protection from seizures was not related to the level of ketosis in the blood, indicating that mechanism(s) of action other than those directly linked to the blood concentration of KBs should be investigated. Most researchers suggest that the metabolic mechanism(s) activated by ketogenic diets (see above) may influence neurotransmitter activity in neurons and this is currently a field of active research. Although the mechanisms of action are not clear, the ketogenic diet is now considered an established part of an integrative approach, along with drug therapy, in the major epilepsy centres worldwide,42 an important benefit being the reduction of drug use and concomitant reductions in severe side effects often associated with antiepileptic agents. The effectiveness of ketogenic diets is strongly supported in a recent Cochrane review where all studies showed a 30–40% reduction in seizures compared with comparative controls, and the review authors reported that in children the effects were ‘comparable to modern antiepileptic drugs'. The main drawback with the ketogenic diet was difficult tolerability and high dropout rates—given the extremely positive results and the severe side effects common with antiepilepsy medication, the development of an easier-to-follow ketogenic diet would be a worthwhile goal.5

In conclusion, the role of ketogenic diets in epilepsy treatment is well established and we are confident that this is also the case for weight loss, cardiovascular disease and T2D. The recent research reviewed here demonstrate improvements in many risk factors, such as weight, saturated fats, inflammation and other biomarkers, as a consequence of consuming well-formulated low-carbohydrate diets, and this work should encourage continued close examination of their therapeutic value (Figure 1).

Emerging evidence

In recent years there have been an increasing number of studies published, suggesting that at least for certain food types there is a nutritional influence on the development of acne. The negative effects seem to lie in the capacity of some foods/nutrients to stimulate proliferative pathways that in turn stimulate development of acne—suspect foods include those with a high glycaemic load and milk.11, 43, 44 Other evidence comes from several studies reporting that the prevalence of acne varies significantly between different populations and is substantially lower in non-Westernized populations that follow traditional diets,45 a common factor among these traditional diets being a low glycaemic load.46 Various studies have provided evidence that high-glycaemic-load diets are implicated in the aetiology of acne through their capacity to stimulate insulin, androgen bioavailability and insulin-like growth factor-1 (IGF-1) activity, whereas the beneficial effects of low-glycaemic-load diets, apart from weight and blood glucose levels, also include improved skin quality.44 The clinical and experimental evidence does in fact suggest ways in which insulin can increase androgen production and affect via induction of steroidogenic enzymes,47 the secretion by the pituitary gland of gonadotropin-releasing hormone and the production of sex hormone-binding globulin.48 Insulin is also able to reduce serum levels of IGF-binding protein-1 increasing the effect of IGF-1.49 These insulin-mediated actions can therefore influence diverse factors that underlie the development of acne such as:

  1. The increased proliferation of basal keratinocytes within the pilosebaceous ducts.
  2. An abnormal desquamation of the follicular epithelium.
  3. Increased androgen-mediated sebum production.
  4. Colonization of the stratum corneum by Propionibacterium acnes and consequent inflammation.46

In summary, there is persuasive, although not yet conclusive, clinical and physiological evidence that the ketogenic diet could be effective in reducing the severity and progression of acne and randomized clinical trials will be required to resolve the issue.11


Carcinogenesis is a complex process involving multiple sequential mutations, which occur randomly in the DNA of normal cells over many years, even decades, until finally specific genes are mutated and cell growth becomes out of control resulting in the full neoplastic phenotype and often metastasis. There is evidence that hyperinsulinaemia, hyperglycaemia and chronic inflammation may affect the neoplastic process through various pathways, including the insulin/IGF-1 pathway, and most cancer cells express insulin and IGF-1 receptors. Insulin has been shown to stimulate mitogenesis (even in cells lacking IGF-1 receptors)50 and it may also contribute by stimulating multiple cancer mechanisms, including proliferation, protection from apoptotic stimuli, invasion and metastasis.51 The IFG1/insulin pathway may also enhance the promotion and progression of many types of cancer cells and facilitate cancer diffusion through angiogenesis.52 Insulin may act directly, but also indirectly through IGF-1, as it reduces hepatic IGF-binding protein-1 and -2 production,53 thereby increasing the levels of circulating, free active IGF-1, which may have a role in cancerogenesis due to its mitogenic and antiapoptotic activity.53 Considering the obvious relationship between carbohydrates and insulin (and IGF-1) a connection between carbohydrate and cancer is a possible consequence, and some links have been recognized since the 1920s when the Russo-German physician Dr A Braunstein observed that glycosuria falls off notably in diabetic patients who developed cancer.54 Later Warburg et al.55 of the Kaiser Wilheim Institute fur biologie described what was later known as the Warburg effect—where energy is predominantly generated by a high rate of glycolysis followed by lactic acid fermentation in the cytosol, even in the presence of plentiful oxygen.51, 55 The Warburg effect has been confirmed in many studies and today is a well-established hallmark of many types of cancers, and rapidly growing tumour cells typically have glycolytic rates up to 200 times higher than those of their normal tissues of origin.56 As stated above, the stimulus of the insulin/IGF-1 pathway is involved in cancer development, but also mitochondrial damage or dysfunction may have a role.18, 57, 58 Dysfunctional mitochondria may upregulate some oncogenes of the phosphatidylinositol 3-kinase/Akt mammalian target of rapamycin signalling pathway.58 Akt, a downstream of insulin signalling,59 is involved in changes in tumour cell metabolism and increases resistance to apoptosis; it also decreases β-oxidation and increases lipid synthesis in the cytosol.60 Hence, it seems a reasonable possibility that a very-low-carbohydrate diet could help to reduce the progression of some types of cancer, although at present the evidence is preliminary.61 In the 1980s, seminal animal studies by Tisdale and colleagues62, 63 demonstrated that a ketogenic diet was capable to reduce tumour size in mice, whereas more recent research has provided evidence that ketogenic diets may reduce tumour progression in humans, at least as far as gastric and brain cancers are concerned.64, 65, 66, 67 Although no randomized controlled trials with VLCKD have yet been conducted on patients and the bulk of evidence in relation to the influence of VLCKD on patient survival is still anecdotal,68, 69, 70 a very recent paper by Fine et al.71 suggests that the insulin inhibition caused by a ketogenic diet could be a feasible adjunctive treatment for patients with cancer. In summary, perhaps through glucose ‘starvation' of tumour cells and by reducing the effect of direct insulin-related actions on cell growth, ketogenic diets show promise as an aid in at least some kind of cancer therapy and is deserving of further and deeper investigation—certainly the evidence justifies setting up clinical trials.

Polycystic ovary syndrome

Polycystic ovary syndrome (PCOS) is a common endocrine disorder in females, with a high prevalence (6–10%);72 symptoms include hyperandrogenism, ovulatory dysfunction, obesity, insulin resistance and subfertility. Insulin resistance and related hyperinsulinaemia is actually a very common feature affecting about 65–70% of women with PCOS;73 it is seen most frequently in obese patients, affecting 70–80%, compared with only 20–25% of lean PCOS sufferers.72 Despite this observation, insulin resistance and hyperinsulinaemia appear to be linked to PCOS independently of obesity, and modifications in the normal cellular mechanisms of insulin signalling have been demonstrated in both lean and obese patients. Furthermore, high blood levels of insulin can act by increasing androgenous hormonal stimulation of the ovarian theca cells as well as potentiating gonadotropin-stimulated ovarian androgen steroidogenesis—although recent data has suggested that the insulin-induced increase in ovarian hormone secretion is not accompanied by increased steroid metabolism.74 Hyperinsulinaemia may also affect the central actions of androgen by impairing progesterone inhibition of the gonadotropin-releasing hormone pulse generator.75 Insulin has also been shown to increase expression of adrenal steroidogenic enzyme mRNA47 as well as adrenal responsiveness to adrenocorticotropic hormone.76

Women with PCOS frequently demonstrate many of the signs related to metabolic syndrome, such as insulin resistance, obesity, glucose intolerance, T2D, dyslipidemia and also high levels of inflammation. Suggested treatments include those that reduce insulin resistance/hyperinsulinaemia, such as lifestyle modifications (exercise, diet and weight loss) and pharmacological treatments that include the administration of thiazolidinediones or metformin. It is evident that any interventions that improve insulinaemia and reduce body weight may also be effective in reducing hyperandrogenism, normalizing ovulation and reducing the various symptoms of PCOS.

Finally, although we only have preliminary evidence of the positive effects of VLCKD in PCOS,77 there are clear mechanisms that are consistent with the physiological plausibility of such dietary therapy.

Neurological diseases

Emerging data suggest a possible therapeutic utilization of ketogenic diets in multiple neurological disorders apart from epilepsy,78 including head ache, neurotrauma, Alzheimer's and Parkinson's disease, sleep disorders, brain cancer, autism and multiple sclerosis.79 Although these various diseases are clearly different from each other, a common basis potentially explaining ketogenic diet efficacy could be a neuroprotective effect in any disease in which the pathogenesis includes abnormalities in cellular energy utilization, which is a common characteristic in many neurological disorders.79 The exact mechanism(s) by which a ketogenic diet may act is still poorly understood; however, some published reports can provide useful suggestions. For example, KBs were recently reported to act as neuroprotective agents by raising ATP levels and reducing the production of reactive oxygen species in neurological tissues,80 together with increased mitochondrial biogenesis, which may help to enhance the regulation of synaptic function.80 Moreover, the increased synthesis of polyunsaturated fatty acids stimulated by a KD may have a role in the regulation of neuronal membrane excitability: it has been demonstrated, for example, that polyunsaturated fatty acids modulate the excitability of neurons by blocking voltage-gated sodium channels.81 Another possibility is that by reducing glucose metabolism, ketogenic diets may activate anticonvulsant mechanisms, as has been reported in a rat model.82 In addition, caloric restriction per se has been suggested to exert neuroprotective effects, including improved mitochondrial function, decreased oxidative stress and apoptosis, and inhibition of proinflammatory mediators, such as the cytokines tumour necrosis factor-α and interleukins.83 Although promising data have been collected (see below), at the present time the real clinical benefits of ketogenic diets in most neurological diseases remain largely speculative and uncertain, with the significant exception of its use in the treatment of convulsion diseases.

Alzheimer's disease

Patients affected with Alzheimer's disease show a higher incidence of seizures compared with unaffected people,84 and it has recently been reported that neuronal excitability is enhanced,85, 86 and neuronal circuits and mitochondrial homeostasis are altered.87

On the basis of the reports described above, these results indicate a possible role of the ketogenic diet in the treatment of Alzheimer's disease in the clinic. Supporting evidence is provided by a study, which reported that at least in selected conditions a significant clinical improvement was observed in Alzheimer's patients fed a ketogenic diet.88 It was suggested that this was, at least in part, related to improved mitochondrial function secondary to the reported protective effects of KBs against the toxic consequences of the exposure of cultured neurons to β-amyloid.89 In an animal model of Alzheimer's disease, transgenic mice consuming a ketogenic diet exhibited better mitochondrial function and less oxidative stress and β-amyloid deposition when compared with normally fed controls.90 These promising results should encourage further research that is necessary to improve our understanding about the potential benefits of ketogenic diets in this debilitating and, thus far, irreversible disease.

Parkinson's disease

The possible beneficial effects of ketogenic diets on mitochondrial activity described above has also been proposed to explain the improved scores on a standard gravity scale of Parkinson' disease exhibited by some patients.91 In addition, the typical mitochondrial respiratory chain damage that occurs in animal models of Parkinson's disease was reduced by a ketogenic diet;89 however, the real utility of this diet remains largely speculative and uncertain.

Brain trauma

Traumatic brain injury may lead over time to epilepsy. Because of the effective use of the ketogenic diet in reducing seizures (see above), it has been suggested that it may also improve the clinical status in brain injury, especially by reducing the incidence of long-term consequences, such as epilepsy.79 Positive effects of a ketogenic diet have also been reported in reducing the cortical contusion volume in an age-dependent manner in an animal model of cortical injury, which is related to the maturation-dependent variability in brain ketone metabolism.92 These findings were also supported by the demonstration that a ketogenic diet reduced post-traumatic cognitive and motor function impairment, at least in a rat model.93

The antiepileptogenic activity of the ketogenic diet after traumatic brain damage is controversial though,94 and further studies are needed to increase related knowledge.

Amyotrophic lateral sclerosis

Dysfunction in energy production, that is, mitochondrial function impairment, is likely to have a role in the pathogenesis of many neurodegenerative diseases, perhaps including amyotrophic lateral sclerosis. On this basis, a ketogenic diet has been proposed as a collateral therapeutic approach in this disease.95 Studies by Zhao et al.96 revealed both histological and functional improvements in an animal model of amyotrophic lateral sclerosis when a ketogenic diet was given compared with when given a control diet. Although survival time was not increased, a higher motor neuron count and lower motor function impairment was reported among the findings.

Nevertheless, direct experimentation and clinical trials in humans are still lacking at the present time, and to avoid the possibility of generating false hopes the preliminary data from animal models obviously have to be considered very cautiously.

The effect of a ketogenic diet on respiratory function

The metabolic effects of a ketogenic diet imply a higher-than-usual oxidation of fats, which leads in turn to reduced respiratory exchange ratio values.20, 97 Metabolic carbon dioxide output may be calculated as the product of alveolar ventilation multiplied by the fractional alveolar carbon dioxide concentration. Pulmonary ventilation differs from alveolar ventilation only by the amount of physiological dead space, and there is no reason to suspect a change in physiological dead space when a dietary manipulation is applied. Hence, following a ketogenic diet-induced decrement of the respiratory exchange ratio and of metabolic carbon dioxide output, a decrease in arterial carbon dioxide partial pressure or of pulmonary ventilation, or of both, is expected. If verified, these effects might be useful in the treatment of patients with respiratory failure; however, this aspect of the ketogenic diet remains to be investigated. Sabapathy et al.98 observed that the reduction in muscle glycogen content caused a respiratory exchange ratio decrement, which was associated with reduced carbon dioxide partial pressure and constancy of pulmonary ventilation. These findings at least suggest potential useful effects of this diet in patients with increased carbon dioxide, arterial partial-pressure values as a consequence of respiratory failure. Of course, more studies are needed to verify this working hypothesis.

Potential risks of ketogenic diets

If we equate de facto ketogenic diets with high-protein diets (which is not always correct) then the risks proposed by critics of this type of dietary approach are essentially those of possible kidney damage due to high levels of nitrogen excretion during protein metabolism, which can cause an increase in glomerular pressure and hyperfiltration.12 There is not wide agreement between studies; however, some infer the possibility of renal damage from animal studies,99, 100 whereas others, looking at both animal models, meta-analyses and human studies, propose that even high levels of protein in the diet do not damage renal function.101, 102 In subjects with intact renal function, higher dietary protein levels caused some functional and morphological adaptations without negative effects.103 There may actually be renal-related effects, but on blood pressure rather than morphological damage. The amino acids involved in gluconeogenesis and/or production of urea in general have blood-pressure-lowering effects, whereas acidifying amino acids tend to cause a rise in blood pressure. Subjects with renal insufficiency, even subclinical, kidney transplant patients and people with metabolic syndrome or other obesity-related conditions, will be more susceptible to the hypertensive effect of amino acids, especially of the sulphated variety.104 The well-documented correlation between obesity and reduced nephron quantity on raised blood pressure puts subjects with T2D or metabolic syndrome at risk, even if in diabetics with kidney damage the effects are not always consistent with the hypothesis.12,105,106 In fact, although some authors have reported a positive influence of a reduction in protein intake from 1.2 to 0.9 g/kg, over the short term, on albuminuria in T2D,107 the same authors have subsequently stated instead that dietary protein restriction is neither necessary nor useful over the long term.108

Moreover, it should be noted that ketogenic diets are only relatively high in protein18, 106 and that some recent studies have demonstrated that VLCKD can even cause a regression of diabetic nephropathy in mice.109 With regard to possible acidosis during VLCKD, as the concentration of KBs never rises above 8 mmol/l10 this risk is virtually inexistent in subjects with normal insulin function.


Ketogenic diets are commonly considered to be a useful tool for weight control and many studies suggest that they could be more efficient than low-fat diets, although there is not concordance in the literature about their absolute effectiveness and even some doubts raised about safety. But there is a ‘hidden face' of the ketogenic diet: its broader therapeutic action. There are new and exciting scenarios about the use of ketogenic diets, as discussed in this review, in cancer, T2D, PCOS, cardiovascular and neurological diseases. Further studies are warranted to investigate more in detail the potential therapeutic mechanisms, its effectiveness and safety, and we would invite all researchers to face this challenge without prejudice.


The authors declare no conflict of interest.

Atkins RC. Dr Atkins' Diet Revolution: The High Calorie Way to Stay Thin ForeverD. McKay Co: New York, NY, USAYear: 1972
WHOMedicines: Corruption and PharmaceuticalsWHO Fact Sheet, WHOYear: 2009
Veech RL. The therapeutic implications of ketone bodies: The effects of ketone bodies in pathological conditions: ketosis, ketogenic diet, redox states, insulin resistance, and mitochondrial metabolismProstaglandins Leukot Essent Fatty AcidsYear: 20047030931914769489
Owen OE,Morgan AP,Kemp HG,Sullivan JM,Herrera MG,Cahill GF Jr. Brain metabolism during fastingJ Clin InvestYear: 196746158915956061736
Kessler SK,Neal EG,Camfield CS,Kossoff EH. Dietary therapies for epilepsy: future researchEpilepsy BehavYear: 201122172221441072
Fukao T,Lopaschuk GD,Mitchell GA. Pathways and control of ketone body metabolism: on the fringe of lipid biochemistryProstaglandins Leukot Essent Fatty AcidsYear: 20047024325114769483
Veldhorst MA,Westerterp-Plantenga MS,Westerterp KR. Gluconeogenesis and energy expenditure after a high-protein, carbohydrate-free dietAm J Clin NutrYear: 20099051952619640952
Krebs HA. The regulation of the release of ketone bodies by the liverAdv Enzyme RegulYear: 196643393544865971
Paoli A,Canato M,Toniolo L,Bargossi AM,Neri M,Mediati M,et al. The ketogenic diet: an underappreciated therapeutic optionClin TerYear: 2011162e145e15322041813
Cahill GF Jr. Fuel metabolism in starvationAnnu Rev NutrYear: 20062612216848698
Paoli A,Grimaldi K,Toniolo L,Canato M,Bianco A,Fratter A. Nutrition and acne: therapeutic potential of ketogenic dietsSkin Pharmacol PhysiolYear: 20122511111722327146
Westerterp-Plantenga MS,Nieuwenhuizen A,Tome D,Soenen S,Westerterp KR. Dietary protein, weight loss, and weight maintenanceAnnu Rev NutrYear: 200929214119400750
Feinman RD,Fine EJ. Nonequilibrium thermodynamics and energy efficiency in weight loss dietsTheor Biol Med ModelYear: 200742717663761
Freedman MR,King J,Kennedy E. Popular diets: A scientific reviewObes ResYear: 20019(Suppl 11S40S11374180
Brehm BJ,Seeley RJ,Daniels SR,D'Alessio DA. A randomized trial comparing a very low carbohydrate diet and a calorie-restricted low fat diet on body weight and cardiovascular risk factors in healthy womenJ Clin Endocrinol MetabYear: 2003881617162312679447
Gardner CD,Kiazand A,Alhassan S,Kim S,Stafford RS,Balise RR,et al. Comparison of the atkins, zone, ornish, and LEARN diets for change in weight and related risk factors among overweight premenopausal women: The A TO Z weight loss study: a randomized trialJAMAYear: 200729796997717341711
Shai I,Schwarzfuchs D,Henkin Y,Shahar DR,Witkow S,Greenberg I,et al. Weight loss with a low-carbohydrate, mediterranean, or low-fat dietN Engl J MedYear: 200835922924118635428
Fine EJ,Feinman RD. Thermodynamics of weight loss dietsNutr Metab (Lond)Year: 200411515588283
Halton TL,Hu FB. The effects of high protein diets on thermogenesis, satiety and weight loss: a critical reviewJ Am Coll NutrYear: 20042337338515466943
Paoli A,Grimaldi K,Bianco A,Lodi A,Cenci L,Parmagnani A. Medium term effects of a ketogenic diet and a mediterranean diet on resting energy expenditure and respiratory ratioBMC ProceedingsYear: 20126(Suppl 3): P37
Sumithran P,Prendergast LA,Delbridge E,Purcell K,Shulkes A,Kriketos A,et al. Ketosis and appetite-mediating nutrients and hormones after weight lossEur J Clin NutrYear: 2013;e-pub ahead of print 1 May 2013; doi:10.1038/ejcn.2013.90
Veldhorst M,Smeets A,Soenen S,Hochstenbach-Waelen A,Hursel R,Diepvens K,et al. Protein-induced satiety: effects and mechanisms of different proteinsPhysiol BehavYear: 20089430030718282589
Johnstone AM,Horgan GW,Murison SD,Bremner DM,Lobley GE. Effects of a high-protein ketogenic diet on hunger, appetite, and weight loss in obese men feeding ad libitumAm J Clin NutrYear: 200887445518175736
Paoli A,Cenci L,Fancelli M,Parmagnani A,Fratter A,Cucchi A,et al. Ketogenic diet and phytoextracts comparison of the efficacy of mediterranean, zone and tisanoreica diet on some health risk factorsAgro Food Ind Hi-TechYear: 20102124
Nordmann AJ,Nordmann A,Briel M,Keller U,Yancy WS Jr,Brehm BJ,et al. Effects of low-carbohydrate vs low-fat diets on weight loss and cardiovascular risk factors: a meta-analysis of randomized controlled trialsArch Intern MedYear: 200616628529316476868
Blackburn GL,Phillips JC,Morreale S. Physician's guide to popular low-carbohydrate weight-loss dietsCleve Clin J MedYear: 200168761766768–9, 773–4.11563479
Volek JS,Phinney SD,Forsythe CE,Quann EE,Wood RJ,Puglisi MJ,et al. Carbohydrate restriction has a more favorable impact on the metabolic syndrome than a low fat dietLipidsYear: 20094429730919082851
Sharman MJ,Kraemer WJ,Love DM,Avery NG,Gomez AL,Scheett TP,et al. A ketogenic diet favorably affects serum biomarkers for cardiovascular disease in normal-weight menJ NutrYear: 20021321879188512097663
Volek JS,Sharman MJ,Forsythe CE. Modification of lipoproteins by very low-carbohydrate dietsJ NutrYear: 20051351339134215930434
Jornayvaz FR,Samuel VT,Shulman GI. The role of muscle insulin resistance in the pathogenesis of atherogenic dyslipidemia and nonalcoholic fatty liver disease associated with the metabolic syndromeAnnu Rev NutrYear: 20103027329020645852
Hellerstein MK. De novo lipogenesis in humans: Metabolic and regulatory aspectsEur J Clin NutrYear: 199953(Suppl 1S53S6510365981
Bistrian BR,Blackburn GL,Flatt JP,Sizer J,Scrimshaw NS,Sherman M. Nitrogen metabolism and insulin requirements in obese diabetic adults on a protein-sparing modified fastDiabetesYear: 1976254945041278601
Gumbiner B,Wendel JA,McDermott MP. Effects of diet composition and ketosis on glycemia during very-low-energy-diet therapy in obese patients with non-insulin-dependent diabetes mellitusAm J Clin NutrYear: 1996631101158604657
Boden G,Sargrad K,Homko C,Mozzoli M,Stein TP. Effect of a low-carbohydrate diet on appetite, blood glucose levels, and insulin resistance in obese patients with type 2 diabetesAnn Intern MedYear: 200514240341115767618
Dashti HM,Al-Zaid NS,Mathew TC,Al-Mousawi M,Talib H,Asfar SK,et al. Long term effects of ketogenic diet in obese subjects with high cholesterol levelMol Cell BiochemYear: 20062861916652223
Yancy WS Jr,Foy M,Chalecki AM,Vernon MC,Westman EC. A low-carbohydrate, ketogenic diet to treat type 2 diabetesNutr Metab (Lond)Year: 200523416318637
Nielsen JV,Joensson EA. Low-carbohydrate diet in type 2 diabetes: Stable improvement of bodyweight and glycemic control during 44 months follow-upNutr Metab (Lond)Year: 200851418495047
Basu S,Yoffe P,Hills N,Lustig RH. The relationship of sugar to population-level diabetes prevalence: An econometric analysis of repeated cross-sectional dataPLoS OneYear: 20138e5787323460912
Hartman AL,Gasior M,Vining EP,Rogawski MA. The neuropharmacology of the ketogenic dietPediatr NeurolYear: 20073628129217509459
McDaniel SS,Rensing NR,Thio LL,Yamada KA,Wong M. The ketogenic diet inhibits the mammalian target of rapamycin (mTOR) pathwayEpilepsiaYear: 201152e7e1121371020
Hartman AL,Lyle M,Rogawski MA,Gasior M. Efficacy of the ketogenic diet in the 6-hz seizure testEpilepsiaYear: 20084933433918070095
Kossoff E. The fat is in the fire: ketogenic diet for refractory status epilepticusEpilepsy CurrYear: 201111888921852870
Cordain L,Eaton SB,Sebastian A,Mann N,Lindeberg S,Watkins BA,et al. Origins and evolution of the western diet: health implications for the 21st centuryAm J Clin NutrYear: 20058134135415699220
Smith RN,Mann NJ,Braue A,Makelainen H,Varigos GA. The effect of a high-protein, low glycemic-load diet versus a conventional, high glycemic-load diet on biochemical parameters associated with acne vulgaris: A randomized, investigator-masked, controlled trialJ Am Acad DermatolYear: 20075724725617448569
Smith R,Mann N. Acne in adolescence: a role for nutritionNutr DietYear: 200764S147S149
Cordain L. Implications for the role of diet in acneSemin Cutan Med SurgYear: 200524849116092796
Kristiansen SB,Endoh A,Casson PR,Buster JE,Hornsby PJ. Induction of steroidogenic enzyme genes by insulin and IGF-I in cultured adult human adrenocortical cellsSteroidsYear: 1997622582659055386
Goodman-Gruen D,Barrett-Connor E. Sex hormone-binding globulin and glucose tolerance in postmenopausal women. the rancho bernardo studyDiabetes CareYear: 1997206456499096996
Powell DR,Suwanichkul A,Cubbage ML,DePaolis LA,Snuggs MB,Lee PD. Insulin inhibits transcription of the human gene for insulin-like growth factor-binding protein-1J Biol ChemYear: 199126618868188761717456
Denley A,Carroll JM,Brierley GV,Cosgrove L,Wallace J,Forbes B,et al. Differential activation of insulin receptor substrates 1 and 2 by insulin-like growth factor-activated insulin receptorsMol Cell BiolYear: 2007273569357717325037
Giovannucci E,Harlan DM,Archer MC,Bergenstal RM,Gapstur SM,Habel LA,et al. Diabetes and cancer: a consensus reportCA Cancer J ClinYear: 20106020722120554718
Rose DP,Vona-Davis L. The cellular and molecular mechanisms by which insulin influences breast cancer risk and progressionEndocr Relat CancerYear: 201219R225R24122936542
Renehan AG,Frystyk J,Flyvbjerg A. Obesity and cancer risk: the role of the insulin-IGF axisTrends Endocrinol MetabYear: 20061732833616956771
AA.VV. Research in cancerScienceYear: 192562x+xii+xiv.
Warburg O,Wind F,Negelein E. The metabolism of tumors in the bodyJ Gen PhysiolYear: 1927851953019872213
Hanahan D,Weinberg RA. Hallmarks of cancer: the next generationCellYear: 201114464667421376230
Warburg O. On respiratory impairment in cancer cellsScienceYear: 195612426927013351639
Pelicano H,Xu RH,Du M,Feng L,Sasaki R,Carew JS,et al. Mitochondrial respiration defects in cancer cells cause activation of akt survival pathway through a redox-mediated mechanismJ Cell BiolYear: 200617591392317158952
Sandri M,Barberi L,Bijlsma AY,Blaauw B,Dyar KA,Milan G,et al. Signalling pathways regulating muscle mass in ageing skeletal muscle. the role of the IGF1-akt-mTOR-FoxO pathwayBiogerontologyYear: 2013;e-pub ahead of print 19 May 2013.
Schwertfeger KL,McManaman JL,Palmer CA,Neville MC,Anderson SM. Expression of constitutively activated akt in the mammary gland leads to excess lipid synthesis during pregnancy and lactationJ Lipid ResYear: 2003441100111212700340
Klement RJ,Kammerer U. Is there a role for carbohydrate restriction in the treatment and prevention of cancerNutr Metab (Lond)Year: 201187522029671
Tisdale MJ,Brennan RA,Fearon KC. Reduction of weight loss and tumour size in a cachexia model by a high fat dietBr J CancerYear: 19875639433620317
Beck SA,Tisdale MJ. Effect of insulin on weight loss and tumour growth in a cachexia modelBr J CancerYear: 1989596776812736199
Ho VW,Leung K,Hsu A,Luk B,Lai J,Shen SY,et al. A low carbohydrate, high protein diet slows tumor growth and prevents cancer initiationCancer ResYear: 2011714484449321673053
Otto C,Kaemmerer U,Illert B,Muehling B,Pfetzer N,Wittig R,et al. Growth of human gastric cancer cells in nude mice is delayed by a ketogenic diet supplemented with omega-3 fatty acids and medium-chain triglyceridesBMC CancerYear: 2008812218447912
Seyfried BT,Kiebish M,Marsh J,Mukherjee P. Targeting energy metabolism in brain cancer through calorie restriction and the ketogenic dietJ Cancer Res TherYear: 20095(Suppl 1S7S1520009300
Zhou W,Mukherjee P,Kiebish MA,Markis WT,Mantis JG,Seyfried TN. The calorically restricted ketogenic diet, an effective alternative therapy for malignant brain cancerNutr Metab (Lond)Year: 20074517313687
Schmidt M,Pfetzer N,Schwab M,Strauss I,Kammerer U. Effects of a ketogenic diet on the quality of life in 16 patients with advanced cancer: a pilot trialNutr Metab (Lond)Year: 201185421794124
Nebeling LC,Lerner E. Implementing a ketogenic diet based on medium-chain triglyceride oil in pediatric patients with cancerJ Am Diet AssocYear: 1995956936977759747
Nebeling LC,Miraldi F,Shurin SB,Lerner E. Effects of a ketogenic diet on tumor metabolism and nutritional status in pediatric oncology patients: Two case reportsJ Am Coll NutrYear: 1995142022087790697
Fine EJ,Segal-Isaacson CJ,Feinman RD,Herszkopf S,Romano MC,Tomuta N,et al. Targeting insulin inhibition as a metabolic therapy in advanced cancer: a pilot safety and feasibility dietary trial in 10 patientsNutritionYear: 2012281028103522840388
Fauser BC,Tarlatzis BC,Rebar RW,Legro RS,Balen AH,Lobo R,et al. Consensus on women's health aspects of polycystic ovary syndrome (PCOS): the amsterdam ESHRE/ASRM-sponsored 3rd PCOS consensus workshop groupFertil SterilYear: 2012972838. e25.22153789
DeUgarte CM,Bartolucci AA,Azziz R. Prevalence of insulin resistance in the polycystic ovary syndrome using the homeostasis model assessmentFertil SterilYear: 2005831454146015866584
Tosi F,Negri C,Perrone F,Dorizzi R,Castello R,Bonora E,et al. Hyperinsulinemia amplifies GnRH agonist stimulated ovarian steroid secretion in women with polycystic ovary syndromeJ Clin Endocrinol MetabYear: 2012971712171922419715
Blank SK,McCartney CR,Chhabra S,Helm KD,Eagleson CA,Chang RJ,et al. Modulation of gonadotropin-releasing hormone pulse generator sensitivity to progesterone inhibition in hyperandrogenic adolescent girls--implications for regulation of pubertal maturationJ Clin Endocrinol MetabYear: 2009942360236619351732
Moghetti P,Castello R,Negri C,Tosi F,Spiazzi GG,Brun E,et al. Insulin infusion amplifies 17 alpha-hydroxycorticosteroid intermediates response to adrenocorticotropin in hyperandrogenic women: apparent relative impairment of 17,20-lyase activityJ Clin Endocrinol MetabYear: 1996818818868772544
Mavropoulos JC,Yancy WS,Hepburn J,Westman EC. The effects of a low-carbohydrate, ketogenic diet on the polycystic ovary syndrome: a pilot studyNutr Metab (Lond)Year: 200523516359551
Baranano KW,Hartman AL. The ketogenic diet: uses in epilepsy and other neurologic illnessesCurr Treat Options NeurolYear: 20081041041918990309
Stafstrom CE,Rho JM. The ketogenic diet as a treatment paradigm for diverse neurological disordersFront PharmacolYear: 201235922509165
Bough KJ,Rho JM. Anticonvulsant mechanisms of the ketogenic dietEpilepsiaYear: 200748435817241207
Huffman J,Kossoff EH. State of the ketogenic diet(s) in epilepsyCurr Neurol Neurosci RepYear: 2006633234016822355
Garriga-Canut M,Schoenike B,Qazi R,Bergendahl K,Daley TJ,Pfender RM,et al. 2-deoxy-D-glucose reduces epilepsy progression by NRSF-CtBP-dependent metabolic regulation of chromatin structureNat NeurosciYear: 200691382138717041593
Maalouf M,Rho JM,Mattson MP. The neuroprotective properties of calorie restriction, the ketogenic diet, and ketone bodiesBrain Res RevYear: 20095929331518845187
Palop JJ,Mucke L. Epilepsy and cognitive impairments in alzheimer diseaseArch NeurolYear: 20096643544019204149
Roberson ED,Halabisky B,Yoo JW,Yao J,Chin J,Yan F,et al. Amyloid-beta/fyn-induced synaptic, network, and cognitive impairments depend on tau levels in multiple mouse models of alzheimer's diseaseJ NeurosciYear: 20113170071121228179
Noebels J. A perfect storm: converging paths of epilepsy and alzheimer's dementia intersect in the hippocampal formationEpilepsiaYear: 201152(Suppl 1394621214538
Kapogiannis D,Mattson MP. Disrupted energy metabolism and neuronal circuit dysfunction in cognitive impairment and alzheimer's diseaseLancet NeurolYear: 20111018719821147038
Henderson ST,Vogel JL,Barr LJ,Garvin F,Jones JJ,Costantini LC. Study of the ketogenic agent AC-1202 in mild to moderate alzheimer's disease: A randomized, double-blind, placebo-controlled, multicenter trialNutr Metab (Lond)Year: 200963119664276
Kashiwaya Y,Takeshima T,Mori N,Nakashima K,Clarke K,Veech RL. D-beta-hydroxybutyrate protects neurons in models of Alzheimer's and Parkinson's diseaseProc Natl Acad Sci USAYear: 2000975440544410805800
Van der Auwera I,Wera S,Van Leuven F,Henderson ST. A ketogenic diet reduces amyloid beta 40 and 42 in a mouse model of alzheimer's diseaseNutr Metab (Lond)Year: 200522816229744
Vanitallie TB,Nonas C,Di Rocco A,Boyar K,Hyams K,Heymsfield SB. Treatment of parkinson disease with diet-induced hyperketonemia: a feasibility studyNeurologyYear: 20056472873015728303
Prins ML,Fujima LS,Hovda DA. Age-dependent reduction of cortical contusion volume by ketones after traumatic brain injuryJ Neurosci ResYear: 20058241342016180224
Appelberg KS,Hovda DA,Prins ML. The effects of a ketogenic diet on behavioral outcome after controlled cortical impact injury in the juvenile and adult ratJ NeurotraumaYear: 20092649750619231995
Schwartzkroin PA,Wenzel HJ,Lyeth BG,Poon CC,Delance A,Van KC,et al. Does ketogenic diet alter seizure sensitivity and cell loss following fluid percussion injuryEpilepsy ResYear: 201092748420863664
Siva N. Can ketogenic diet slow progression of ALSLancet NeurolYear: 2006547616739298
Zhao Z,Lange DJ,Voustianiouk A,MacGrogan D,Ho L,Suh J,et al. A ketogenic diet as a potential novel therapeutic intervention in amyotrophic lateral sclerosisBMC NeurosciYear: 200672916584562
Tagliabue A,Bertoli S,Trentani C,Borrelli P,Veggiotti P. Effects of the ketogenic diet on nutritional status, resting energy expenditure, and substrate oxidation in patients with medically refractory epilepsy: A 6-month prospective observational studyClin NutrYear: 20123124624922019282
Sabapathy S,Morris NR,Schneider DA. Ventilatory and gas-exchange responses to incremental exercise performed with reduced muscle glycogen contentJ Sci Med SportYear: 2006926727316682251
Jia Y,Hwang SY,House JD,Ogborn MR,Weiler HA,O K,et al. Long-term high intake of whole proteins results in renal damage in pigsJ NutrYear: 20101401646165220668252
Wakefield AP,House JD,Ogborn MR,Weiler HA,Aukema HM. A diet with 35% of energy from protein leads to kidney damage in female sprague-dawley ratsBr J NutrYear: 201118
Skov AR,Haulrik N,Toubro S,Molgaard C,Astrup A. Effect of protein intake on bone mineralization during weight loss: A 6-month trialObes ResYear: 20021043243812055318
Martin WF,Armstrong LE,Rodriguez NR. Dietary protein intake and renal functionNutr Metab (Lond)Year: 200522516174292
Welle S,Nair KS. Relationship of resting metabolic rate to body composition and protein turnoverAm J PhysiolYear: 1990258E990E9982360629
Praga M. Synergy of low nephron number and obesity: A new focus on hyperfiltration nephropathyNephrol Dial TransplantYear: 2005202594259716223782
Eisenstein J,Roberts SB,Dallal G,Saltzman E. High-protein weight-loss diets: are they safe and do they work? A review of the experimental and epidemiologic dataNutr RevYear: 20026018920012144197
Westerterp-Plantenga MS. How are normal, high- or low-protein diets definedBr J NutrYear: 20079721721817298688
Pijls LT,de Vries H,Donker AJ,van Eijk JT. The effect of protein restriction on albuminuria in patients with type 2 diabetes mellitus: A randomized trialNephrol Dial TransplantYear: 1999141445145310383006
Pijls LT,de Vries H,van Eijk JT,Donker AJ. Protein restriction, glomerular filtration rate and albuminuria in patients with type 2 diabetes mellitus: a randomized trialEur J Clin NutrYear: 2002561200120712494305
Poplawski MM,Mastaitis JW,Isoda F,Grosjean F,Zheng F,Mobbs CV. Reversal of diabetic nephropathy by a ketogenic dietPLoS OneYear: 20116e1860421533091

Article Categories:
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Keywords: ketogenic diet, cancer, diabetes, neurological diseases, obesity, cardiovascular diseases.

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