Document Detail

Transthyretin as a novel candidate biomarker for preeclampsia.
Jump to Full Text
MedLine Citation:
PMID:  24940434     Owner:  NLM     Status:  Publisher    
Abstract/OtherAbstract:
Preeclampsia (PE) is considered to be a potentially fatal complication during pregnancy. However, no effective laboratory assessment has been developed to enable early diagnosis and monitoring of PE. The present study aimed to identify differentially expressed transthyretin (TTR) during severe PE and evaluate TTR as a possible biomarker of this disease. TTR levels were determined in the different gestational weeks of normal pregnancy (before 20 weeks, n=41; after 20 weeks, n=39) using enzyme-linked immunosorbent assay (ELISA). TTR concentrations in pregnant females with severe PE (n=43) were compared with those in healthy matched control subjects (n=37) using western blot analysis and ELISA. The median TTR concentration during severe PE in each month of gestation was significantly lower than the concentrations recorded during normal pregnancy. TTR levels in females with severe PE were significantly downregulated compared with the control subjects (P<0.001; area under the curve, 0.834-0.967). Thus, TTR may be used as a potential biomarker of PE.
Authors:
Lei Zhu; Yuxuan Chen; Chongdong Liu; Haiteng Deng; Nawei Zhang; Shengdian Wang; Zhenyu Zhang
Related Documents :
6311154 - Pathology in the ovine foetus caused by an ovine pestivirus.
1881974 - Stereotypic behavior, adrenocortical function, and open field behavior of individually ...
16511994 - Methods for studying interferon tau stimulated genes.
542714 - Colostrum production by ewes and the amounts ingested by lambs.
7480844 - Clinical intracytoplasmic sperm injection (icsi) results from royal north shore hospital.
2699744 - Prenatal diagnosis using sonographic guided cordocentesis.
Publication Detail:
Type:  JOURNAL ARTICLE     Date:  2014-2-18
Journal Detail:
Title:  Experimental and therapeutic medicine     Volume:  7     ISSN:  1792-0981     ISO Abbreviation:  Exp Ther Med     Publication Date:  2014 May 
Date Detail:
Created Date:  2014-6-18     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  101531947     Medline TA:  Exp Ther Med     Country:  -    
Other Details:
Languages:  ENG     Pagination:  1332-1336     Citation Subset:  -    
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:

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

Full Text
Journal Information
Journal ID (nlm-ta): Exp Ther Med
Journal ID (iso-abbrev): Exp Ther Med
Journal ID (publisher-id): ETM
ISSN: 1792-0981
ISSN: 1792-1015
Publisher: D.A. Spandidos
Article Information
Download PDF
Copyright © 2014, Spandidos Publications
open-access:
Received Day: 27 Month: 8 Year: 2013
Accepted Day: 17 Month: 1 Year: 2014
Print publication date: Month: 5 Year: 2014
Electronic publication date: Day: 18 Month: 2 Year: 2014
pmc-release publication date: Day: 18 Month: 2 Year: 2014
Volume: 7 Issue: 5
First Page: 1332 Last Page: 1336
PubMed Id: 24940434
ID: 3991523
DOI: 10.3892/etm.2014.1558
Publisher Id: etm-07-05-1332

Transthyretin as a novel candidate biomarker for preeclampsia
LEI ZHU1
YUXUAN CHEN1
CHONGDONG LIU1
HAITENG DENG2
NAWEI ZHANG1
SHENGDIAN WANG3
ZHENYU ZHANG1
1Department of Obstetrics and Gynecology, Beijing Chaoyang Hospital Affiliated to Capital Medical University, Beijing 100020, P.R. China
2The Rockefeller University, New York, NY 10065, USA
3Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, P.R. China
Correspondence: Correspondence to: Professor Zhenyu Zhang, Department of Obstetrics and Gynecology, Beijing Chaoyang Hospital affiliated to Capital Medical University, 8 Baijiazhuang Rd, Beijing 100020, P.R. China, E-mail: zhenyuzhangcn@126.com

Introduction

Preeclampsia (PE) is a multisystem syndrome affecting pregnant females. PE usually develops after 20 weeks of gestation and affects 4–10% of pregnant females. PE is characterized by several symptoms, including hypertension, proteinuria and additional complications such as liver and kidney failure and fetal distress. Approximately 25% of babies born to females with PE are smaller than normal for the particular gestational age. PE is a predominant cause of maternal morbidity and mortality worldwide (1,2). Although the exact determinants of PE remain unclear, placental ischemia is considered to be important in the development. The hypoxic placenta may lead to an imbalance in the release of circulating factors, which may result in widespread vascular endothelial injury. Certain proteomic factors, including antiangiogenic factors, may contribute to systemic hypertension, vascular injury and disorders of the coagulation system (35). Variations in these circulating proteomic factors have been shown to correlate with pathophysiological changes in the disease.

Early diagnosis of PE is reliant upon the provision of regular antenatal care prior to delivery. To date, no biomarker-based laboratory assessment is able to diagnose PE. Investigations have been conducted to identify non-invasive, blood-borne or urinary maternal biomarkers that predict the development of PE and aid in the monitoring of this severe complication during pregnancy (1,6). Potential biochemical markers, including soluble fms-like tyrosine kinase 1 (sflt-1) and placental growth factor (PLGF), have been identified, however are not considered to be reliable in the diagnosis of PE (1,5,6). Therefore, identification of effective markers is required to predict PE.

In a previous study, serum proteomic analysis of PE was performed, revealing decreased transthyretin (TTR) concentrations in the sera of females with PE (7). TTR is a tetrameric serum protein composed of four identical subunits (55 kDa) and is predominantly synthesized in the liver, eye and choroid plexus. A protein group comprising TTR, thyroxin-binding globulin and albumin, bind to and transport thyroid hormones in the blood; the main function of TTR is the transport of thyroxin (T4) (8). TTR is synthesized by placental trophoblasts which are critical to normal fetal development. Thus, disorders caused by TTR production may result in fetal distress (911). In addition, >100 TTR mutations have been shown to be associated with amyloid diseases, which induce tissue-selective deposition of amyloid to various organs (12,13). In a previous study, TTR was shown to be upregulated by two-fold in pancreatic cancer, thus, it was concluded that TTR may be used as a novel tumor marker (14). However, whether TTR may be used as a biomarker of PE remains unknown.

In the present study, significant changes in TTR expression levels during severe PE were observed. It was hypothesized that the differences in TTR concentrations during severe PE were associated with disease pathophysiology, thus, TTR may be a candidate biomarker of PE.


Materials and methods
Grouping

Three experiments were conducted to identify the changes in TTR levels during severe PE. Changes in TTR levels during healthy pregnancy were observed as follows: A series of samples were collected from normal pregnant females at different gestation periods to identify the TTR concentrations during healthy gestation (before 20 weeks, n=41; after 20 weeks, n=39). TTR levels in females with severe PE were compared with the levels of those in the normal control subject group. A total of 43 females after 20 weeks of gestation were selected as participants in the severe PE group; these females were free of other pregnancy complications. No subjects had a history of hypertension or renal disease. A total of 37 healthy females were enrolled in the control group and matched to the females in the severe PE group with regard to gestational age. TTR levels in the severe PE and control groups were monitored simultaneously. TTR levels in the early (n=21) and late (n=22) onset PE patients were compared (all of these cases were included in the severe PE group). The characteristics of participants are presented in Tables IIII. The serum samples were all collected from Chinese females.

Severe PE is defined as an increase in blood pressure (≥160 mmHg systolic pressure or ≥110 mmHg diastolic pressure on more than two occasions at an interval of at least 6 h) that occurs following 20 weeks of gestation in females with normal blood pressure, accompanied by proteinuria (serum protein ≥5 g/24 h or ≥2+ calculated via dipstick measurement), coagulopathy disorders (platelets <100×109/l or disseminated intravascular coagulation), liver dysfunction and acute renal disorders.

Sample collection

Samples were collected from the peripheral blood and prepared by centrifugation at 2,415 × g for 10 min at 4°C within 4 h following acquisition. Samples were subsequently stored at −80°C until use. The samples were collected from the Department of Obstetrics and Gynecology of Beijing Chaoyang Hospital affiliated to Capital Medical University (Beijing, China). This study was approved by the Ethics Committee of Beijing Chaoyang Hospital affiliated to Capital Medical University and informed consent was provided by each participant.

Western blot analysis

TTR expression levels in severe PE and healthy control subjects were evaluated by western blot analysis (severe PE, n=43; control subjects, n=37). Total serum protein concentrations were determined using the bicinchoninic acid assay method (BCA Protein Assay Reagent; Thermo, Rockford, IL, USA). Samples of 60 μg serum protein from the two groups were run on 15% sodium dodecyl sulfate-polyacrylamide gel electrophoresis. The proteins were transferred to nitrocellulose membranes (Millipore Corporation, Billerica, MA, USA) and subjected to 300 mV for 25 min. The membranes were blocked overnight at 4°C in blocking buffer (containing 5% skimmed milk, 0.1% Tween 20 and 0.01 M tris-buffered saline) and incubated with primary antibodies against TTR (mouse monoclonal antibody, 1:1,000 dilution; Abcam, Cambridge, UK) for 120 min at room temperature. The membranes were incubated with goat anti-mouse IgG secondary antibody (Santa Cruz Biotechnology, Inc., Dallas, TX, USA) for 50 min. Protein levels were analyzed by evaluation of the total signal intensities of the western blot bands.

Identification of TTR levels using an enzyme-linked immunosorbent assay (ELISA)

Serum TTR levels were determined by ELISA (Assaypro, St. Charles, MO, USA). Samples were diluted for detection (1:40,000)and the data were presented using CurveExpert 1.3.

Statistical analysis

Data were analyzed using SPSS 17.0 software (SPSS, Inc, Chicago, IL, USA) with the independent samples t-test. P<0.05 was considered to indicate a statistically significant difference. The diagnostic value of TTR for severe PE was determined based on receiver operating characteristic (ROC) curves which were analyzed using MedCalc 9.6.2.0 (MedCalc Software bvba, Ostend, Belgium).


Results
Detection of TTR concentrations during healthy pregnancy

TTR concentrations in the three trimesters of normal pregnancy were determined using ELISA kits (Fig. 1). TTR levels significantly increased in the third month of gestation and rapidly decreased following 20 weeks of gestation. TTR levels in the initial 20 weeks of gestation were considerably higher compared with those following 20 weeks of gestation (P<0.001). No further changes in TTR levels were observed thereafter.

Western blot analysis of TTR changes during severe PE

TTR expression levels were detected by western blot analysis to directly monitor the changes in TTR during severe PE. A total of 43 females with severe PE and 37 control subjects were enrolled in the present study. Fig. 2 shows the expression levels of TTR in the sera of the two groups. The single band at ~16 kDa represented the TTR monomer undergoing dissociation. TTR expression levels were markedly decreased in the sera of patients with severe PE and were ~2.6 times lower compared with the control subjects (4,867±3,464 vs. 12,517±8,516 OD units in the severe PE and control subjects, respectively; P<0.001).

Identification of TTR levels during severe PE using ELISA

ELISA analysis was conducted to quantify the TTR levels of the patients in the severe PE (n=43) and control (n=37) groups. TTR levels significantly decreased in the severe PE group (P<0.001) and were ~2.4 times lower compared with the control group. This result is consistent with those of the western blot analysis. The median TTR concentration of the severe PE group was significantly lower compared with the control group (Fig. 3). In Fig. 1, the median TTR concentrations in the severe PE and healthy subjects at the same gestation period were compared. The curve for the severe PE group was significantly lower than that for the healthy pregnancy group.

TTR levels in early and late onset PE

Among the 43 participants in the severe PE group, 21 individuals were assigned to the early onset group and 22 individuals were assigned to the late onset group. TTR levels were lower in the early onset patients than in the late onset group (P<0.001).

Diagnostic value of TTR for severe PE

The diagnostic value of TTR in severe PE pregnancies was examined with ROC curves (Fig. 4). The results indicated that TTR may be a reliable biomarker for the diagnosis of severe PE, exhibiting sensitivity and specificity levels of 88.4 and 86.5%, respectively (area under the curve, 0.917, range, 0.834–0.967), at a diagnostic value of 128.81 mg/l.


Discussion

The identification of novel and effective biomarkers of PE is critical for early prediction, prognosis, monitoring and treatment responses. Angiogenic factors, including sflt-1 and PLGF, have been considered as potential biomarkers of PE. However, previous studies have presented inconsistencies with regard to the use of various potential markers to diagnose PE. Therefore, further studies are required to identify and develop effective and efficient biomarkers of PE (1,15).

ELISA analysis results of healthy pregnant subjects identified that TTR concentrations rapidly increased in the third month of pregnancy (9–12 weeks). TTR levels were higher prior to 20 weeks of gestation. Administration of maternal thyroid hormone to facilitate fetal development contributes to the rapid increase in TTR levels in the early stages of gestation (10,11,16). A previous study identified that fetuses are unable to synthesize TTR prior to 16 weeks of gestation. In addition, Fig. 3 shows that the highest TTR levels were observed during the third month (9–12 weeks). Lower TTR levels were observed following the fifth month (17–20 weeks) of gestation. Therefore, this result is consistent with results of a previous study, which indicated that maternal TTR proteins may be important in transporting thyroid hormone to the fetus and may be required for fetal development (17). Lower cord serum levels of T4 in preterm infants have been shown to correlate with gestation week and weight. In contrast to term infants, preterm infants frequently experience a decrease in serum T4 levels, which may account for the increased rate of morbidity and mortality (18). These results indicate that the thyroid gland of the fetus does not provide adequate quantities of T4 prior to full term delivery and the maternal thyroid hormone compensates for such insufficient T4 levels during fetal development. Maternal TTR, as a transporter of thyroid hormone, functions in transporting T4 to the fetus (11). Although fetuses may produce TTR proteins, maternal TTR protein may be important in fetal development.

The present study revealed that TTR levels were significantly decreased in the sera of females with severe PE. This result was consistent with that of a previous proteomic analysis, in which decreased levels of TTR were observed in early onset cases of severe PE (19). The median maternal TTR levels were significantly lower in the severe PE group than in the control group. In addition, the curve for the severe PE group was markedly lower compared with the control group in the equivalent gestation month, indicating that the changes in TTR levels during severe PE may correlate with disease development. ROC curves were used to evaluate the reliability of TTR as a diagnostic tool for severe PE (Fig. 4). TTR levels were capable of discriminating between severe PE and healthy females (sensitivity and specificity of 88.4 and 86.5%, respectively) at a cutoff value of 128.81 mg/l.

TTR concentrations in early and late onset cases of severe PE were compared. Diagnosis at earlier gestational stages has been reported to indicate a higher risk of maternal and fetal mortality (20,21). In the present study, TTR levels were markedly decreased in early onset severe PE cases, indicating that the changes in TTR levels may correlate with the severity of PE. Furthermore, these changes may be used to monitor severe complications.

In the present study, two hypotheses were presented to explain the changes in TTR levels during severe PE. Initially, it was hypothesized that the decreased TTR levels may contribute to the pathology of PE. Maternal vascular dysfunction, that induces multi-organ disorders, was considered to be the basic pathological manifestation of PE (3,4,22). The TTR tetramer dissociates to produce a non-native TTR monomer with low conformational stability, thereby forming TTR amyloids, which bind to the vascular wall and lead to changes in membrane fluidity (2325). Therefore, TTR may damage the maternal vascular system via amyloid deposition and this condition may be attributed to the decreased TTR levels during severe PE. TTR amyloid fibrils may be selectively deposited in the maternal vascular system, resulting in organ ischemia of the placenta, liver, kidney and brain, as well as other clinical manifestations (2629). Therefore, TTR concentrations may change prior to the onset of PE and may be used as a potential biomarker to predict and monitor PE. The second hypothesis suggested that the changes in the TTR levels of the severe PE group may have resulted from reduced production of the TTR protein. Previous studies have identified that females with PE exhibit a greater risk of subclinical hypothyroidism during pregnancy, which is attributed to vascular endothelial growth factor inhibitors that damage the endothelium of thyroid capillaries; subclinical hypothyroidism is also involved in reducing the production of thyroid hormone (30). Decreased TTR expression may also be responsible for vascular injury of the placenta. TTR secreted from the placenta is involved in the transport of the maternal thyroid hormone into the fetal circulation via the TTR-T4 complex, which is important in fetal development (10,11,18). As the predominant pathological mechanism of changes in PE, placenta necrosis may result in decreased TTR secretion and lead to disorders during fetal development under severe PE conditions. If the 2nd hypothesis is correct, the decreased level of TTR should be a result of PE pathological variations and may be it is not lower than normal before PE is diagnosed and may not be able to be a predictor of PE. However, hormonal secretion by the placenta may be impaired by continued placenta necrosis, resulting in a further decrease in TTR expression in maternal serum. Therefore, lower maternal TTR levels may indicate that PE has worsened.

In conclusion, the present study has revealed that TTR levels are significantly decreased in severe PE and may be associated with the various changes observed during PE. Therefore, TTR may be used as a candidate biomarker of PE. However, further studies are required to confirm whether TTR functions in the pathology of PE and whether TTR levels change during mild PE. Thus, changes in TTR concentrations prior to the onset of PE require further investigation.


Acknowledgements

The authors thank Professor Shengdian Wang for his technical assistance. The study was supported by grants from the Sino-US Cooperation Funds (no. 2007DFA31080) and NIDCR/NIH (no. U19 DE018385).


References
1. Grill S,Rusterholz C,Zanetti-Dällenbach R,et al. Potential markers of preeclampsia - a reviewReprod Biol Endocrinol770Year: 200919602262
2. Sibai B,Dekker G,Kupferminc M. Pre-eclampsiaLancet365785799Year: 200515733721
3. Dekker GA,Sibai BM. Etiology and pathogenesis of preeclampsia: current conceptsAm J Obstet Gynecol17913591375Year: 19989822529
4. Hacker NF,Gambone JC,Hobel CJHacker and Moore’s Essentials of Obstetrics and Gynecology5th editionElsevier and SaundersPhiladelphia, PA, USAYear: 2010
5. Chaiworapongsa T,Romero R,Espinoza J,et al. Evidence supporting a role for blockade of the vascular endothelial growth factor system in the pathophysiology of preeclampsiaYoung Investigator AwardAm J Obstet Gynecol19015411550Year: 200415284729
6. Maynard SE,Min JY,Merchan J,et al. Excess placental soluble fms-like tyrosine kinase 1 (sFlt1) may contribute to endothelial dysfunction, hypertension, and proteinuria in preeclampsiaJ Clin Invest111649658Year: 200312618519
7. Liu C,Zhang N,Yu H,Chen Y,Liang Y,Deng H,Zhang Z. Proteomic analysis of human serum for Finding pathogenic factors and potential biomarkers in preeclampsiaPlacenta32168174Year: 201121145106
8. Fleming CE,Nunes AF,Sousa MM. Transthyretin: more than meets the eyeProg Neurobiol89266276Year: 200919665514
9. Su PH,Wang SL,Chen JY,Hu JM,Chang HP,Chen SJ. Transthyretin levels are not related to Apgar score in low birth weight and very low birth weight infantsEarly Hum Dev84533538Year: 200818252270
10. McKinnon B,Li H,Richard K,Mortimer R. Synthesis of thyroid hormone binding proteins transthyretin and albumin by human trophoblastJ Clin Endocrinol Metab9067146720Year: 200516159939
11. Landers KA,McKinnon BD,Li H,Subramaniam VN,Mortimer RH,Richard K. Carrier-mediated thyroid hormone transport into placenta by placental transthyretinJ Clin Endocrinol Metab9426102616Year: 200919401362
12. Wiseman RL,Powers ET,Kelly JW. Partitioning conformational intermediates between competing refolding and aggregation pathways: insights into transthyretin amyloid diseaseBiochemistry441661216623Year: 200516342952
13. Saraiva MJ. Transthyretin mutations in hyperthyroxinemia and amyloid diseasesHum Mutat17493503Year: 200111385707
14. Lv S,Gao J,Zhu F,et al. Transthyretin, identified by proteomics, is overabundant in pancreatic juice from pancreatic carcinoma and originates from pancreatic isletsDiagn Cytopathol39875881Year: 201120949480
15. Conde-Agudelo A,Villar J,Lindheimer M. World Health Organization systematic review of screening tests for preeclampsiaObstet Gynecol10413671391Year: 200415572504
16. Ahmed OM,El-Gareib AW,El-Bakry AM,Abd El-Tawab SM,Ahmed RG. Thyroid hormones states and brain development interactionsInt J Dev Neurosci26147209Year: 200818031969
17. Haddow JE,Palomaki GE,Allan WC,et al. Maternal thyroid deficiency during pregnancy and subsequent neuropsychological development of the childN Engl J Med341549555Year: 199910451459
18. LaFranchi S. Thyroid function in the preterm infantThyroid97178Year: 199910037080
19. Pecks U,Seidenspinner F,Röwer C,Reimer T,Rath W,Glocker MO. Multifactorial analysis of affinity-mass spectrometry data from serum protein samples: a strategy to distinguish patients with preeclampsia from matching control individualsJ Am Soc Mass Spectrom2116991711Year: 201020116281
20. Espinoza J,Romero R,Nien JK,et al. Identification of patients at risk for early onset and/or severe preeclampsia with the use of uterine artery Doppler velocimetry and placental growth factorAm J Obstet Gynecol196326Year: 200717403407
21. Llurba E,Carreras E,Gratacós E,et al. Maternal history and uterine artery Doppler in the assessment of risk for development of early- and late-onset preeclampsia and intrauterine growth restrictionObstet Gynecol Int2009275613Year: 200919936122
22. Than NG,Romero R,Hillermann R,Cozzi V,Nie G,Huppertz B. Prediction of preeclampsia - a workshop reportPlacenta29Suppl AS83S85Year: 200818061661
23. Reixach N,Deechongkit S,Jiang X,Kelly JW,Buxbaum JN. Tissue damage in the amyloidoses: Transthyretin monomers and nonnative oligomers are the major cytotoxic species in tissue cultureProc Natl Acad Sci USA10128172822Year: 200414981241
24. Schweigert FJ,Wirth K,Raila J. Characterization of the microheterogeneity of transthyretin in plasma and urine using SELDI-TOF-MS immunoassayProteome Sci25Year: 200415341658
25. Hughes SE,McKenna WJ. New insights into the pathology of inherited cardiomyopathyHeart91257264Year: 200515657260
26. Connors LH,Prokaeva T,Lim A,et al. Cardiac amyloidosis in African Americans: comparison of clinical and laboratory features of transthyretin V122I amyloidosis and immunoglobulin light chain amyloidosisAm Heart J158607614Year: 200919781421
27. Lavatelli F,Perlman DH,Spencer B,et al. Amyloidogenic and associated proteins in systemic amyloidosis proteome of adipose tissueMol Cell Proteomics715701583Year: 200818474516
28. Hou X,Richardson SJ,Aguilar MI,Small DH. Binding of amyloidogenic transthyretin to the plasma membrane alters membrane fluidity and induces neurotoxicityBiochemistry441161811627Year: 200516114899
29. Chen Y,Zhang Z. Does transthyretin function as one of contributors for preeclampsia?Med Hypotheses76810Year: 201120826058
30. Levine RJ,Vatten LJ,Horowitz GL,et al. Pre-eclampsia, soluble fms-like tyrosine kinase 1, and the risk of reduced thyroid function: nested case-control and population based studyBMJ339b4336Year: 200919920004

Article Categories:
  • Articles

Keywords: serum biomarker, preeclampsia, transthyretin.

Previous Document:  Effect of Quanzhenyiqitang on apoptosis of alveolar macrophages and expression of histone deacetylas...
Next Document:  Association between pelvic organ prolapse and stress urinary incontinence with collagen.