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The NIH Undiagnosed Diseases Program: bonding scientists and clinicians.
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MedLine Citation:
PMID:  22228787     Owner:  NLM     Status:  MEDLINE    
The majority of the biomedical research workforce and funds are focused on studying common diseases and the development of drugs to treat them. However, some of the most remarkable discoveries in physiology and medicine are uncovered by studying rare conditions, because the importance of certain molecular mechanisms is revealed only when their dysfunction results in disease. In 2008, the National Institutes of Health (NIH) launched the NIH Undiagnosed Diseases Program (UDP), which recruits and selects patients who suffer from diseases of unknown etiology, and studies their causes at the clinical, genetic and cellular levels. In this Editorial, we discuss how the UDP has enabled the discovery of several new diseases and disease mechanisms through collaborations between clinical and basic science teams, using the power of both clinical medicine and biological models. Establishing programs with similar infrastructure at other centers around the world could help to benefit patients, their families and the entire medical community, by enhancing research productivity for rare and novel diseases.
William A Gahl; Cornelius F Boerkoel; Manfred Boehm
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Publication Detail:
Type:  Editorial; Research Support, N.I.H., Extramural    
Journal Detail:
Title:  Disease models & mechanisms     Volume:  5     ISSN:  1754-8411     ISO Abbreviation:  Dis Model Mech     Publication Date:  2012 Jan 
Date Detail:
Created Date:  2012-01-09     Completed Date:  2012-05-01     Revised Date:  2013-06-26    
Medline Journal Info:
Nlm Unique ID:  101483332     Medline TA:  Dis Model Mech     Country:  England    
Other Details:
Languages:  eng     Pagination:  3-5     Citation Subset:  IM    
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MeSH Terms
Mutation / genetics
National Institutes of Health (U.S.) / organization & administration*
Rare Diseases / diagnosis*,  etiology*,  genetics,  physiopathology
Research Personnel*
Translational Medical Research / manpower,  organization & administration*
United States

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

Full Text
Journal Information
Journal ID (nlm-ta): Dis Model Mech
Journal ID (hwp): dmm
Journal ID (publisher-id): DMM
ISSN: 1754-8403
ISSN: 1754-8411
Publisher: The Company of Biologists Limited
Article Information
© 2012. Published by The Company of Biologists Ltd
Print publication date: Month: 1 Year: 2012
Volume: 5 Issue: 1
First Page: 3 Last Page: 5
ID: 3255536
PubMed Id: 22228787
DOI: 10.1242/dmm.009258
Publisher Id: 0050003

The NIH Undiagnosed Diseases Program: bonding scientists and clinicians
William A. Gahl12*
Cornelius F. Boerkoel2
Manfred Boehm3
1Office of the Clinical Director, NHGRI, NIH, Building 10, Room 10C103, 10 Center Drive, MSC-1851, Bethesda, MD 20892-1851, USA
2NIH Undiagnosed Diseases Program, NIH, 9 Memorial Drive, Room 1N113, Bethesda, MD 20892, USA
3National Heart, Lung and Blood Institute, NIH, Building 31, Room 5A52, 31 Center Drive MSC 2486, Bethesda, MD 20892, USA
*Author for correspondence (

“As our knowledge and data in genetics burgeon, we must engage the cognoscenti in a wide variety of fields to discover new diseases, new mechanisms of action and, ultimately, new therapeutic interventions”


Natural selection solidifies the most favorable alterations in our replicative processes to create brilliantly functional biochemical and cellular pathways. By contrast, less favorable genetic changes or ‘errors’ disrupt nature’s beautifully honed systems. Hence, it is axiomatic that rare diseases, in addition to being coruscating curiosities, also serve as windows to the world’s normal order. Among the women and men who address human mutations, clinicians provide care for those affected with rare maladies, and a special cadre of scientists investigates the causes of those disorders. Together, these two groups employ their expertise to advance treatment and understanding.

The NIH Undiagnosed Diseases Program (UDP), announced May 19, 2008, serves as a focal point for the synergistic interplay between clinical and basic science investigators (Gahl and Tifft, 2011; Gahl et al., 2011). The UDP filters thousands of enquiries down to hundreds of NIH Clinical Center inpatient admissions, and then chooses illustrative cases to pursue experimentally. Three years into its operation, the UDP had reviewed more than 1800 thick medical records, accepted approximately 430 patients and admitted 350 of them. The program had performed close to 600 single nucleotide polymorphism (SNP) arrays and analyzed approximately 230 whole exome sequences (WESs) using DNA from patients and their family members. Many specific cases warranted intense investigation, based on their compelling clinical presentations, the likelihood that the basic defects would be uncovered and the impact predicted to emanate from the ‘new disease discovery’. In the sections below, we recount examples that illustrate the process of disease discovery and how it can, in turn, provide new information about the role of genes and biological pathways in normal and impaired physiology.

Stepwise investigation of an undiagnosed disease

The paradigm for studying such medical mysteries begins with detailed and accurate phenotyping. For example, UDP clinical investigators ascertained a family of five adults from middle America with stunning arterial calcification and claudication confined to the lower extremities (St. Hilaire et al., 2011). Intense clinical examinations verified that this was not atherosclerosis, that the coronaries were spared, and that the only additional sites of ectopic calcification involved the joint capsules of the hands and feet. Endocrine abnormalities of calcium and phosphate were ruled out.

The next step involved applying genetic methodologies to identify candidate genes causing this disease. In this case, the project benefited enormously from the fact that the parents of the five siblings were third cousins, unaffected, and readily available for study. The most appropriate genetic platform to employ was the million SNP array, which detects copy number variants (deletions and duplications) and also identifies regions of homozygosity. In a product of a consanguineous mating, most homozygous areas derive from a common ancestor, and a single pathogenic mutation in a shared ancestral gene could cause a recessive disease. Hence, we were looking for a region of the human genome in which all five affected siblings were homozygous, but the parents were heterozygous. Only one area satisfied these requirements – a 22-Mb region on chromosome 6. That area contained 92 genes; any one of them could have contained a homozygous mutation that caused the arterial calcifications. We needed an expert in vascular biology to identify the best candidates to pursue.

This was the third, and most crucial, step in discovering a new human disease, i.e. identifying and connecting with a basic scientist whose lab possessed expertise in the field. In this case, Manfred Boehm and Cynthia St. Hilaire of the National Heart, Lung and Blood Institute were authorities on vascular cell metabolism, and cell-based assays were extant in the Boehm lab. In concert with the UDP, whose clinicians provided a skin biopsy, St. Hilaire cultured an affected patient’s fibroblasts and performed expression analysis of candidate genes in the inherited homozygous region. Only one gene, NT5E, which encodes the CD73 protein, was differentially expressed. Direct sequencing of NT5E identified null mutations that resulted in complete inactivation of CD73 protein in all affected siblings. This newly identified vascular disease was referred to as ‘arterial calcification due to deficiency of CD73′ (ACDC). CD73 is a membrane-bound enzyme that converts extracellular AMP to adenosine and inorganic phosphate; this process was found to be severely impaired in fibroblasts from individuals with ACDC. The failure to generate extracellular adenosine leads to an increase in tissue non-specific alkaline phosphatase (TNAP), a key enzyme in tissue calcification in vitro and in vivo. Cultured fibroblasts of individuals with ACDC not only contained increased TNAP activity, but they also calcified. Finally, TNAP activity and in vitro calcification could be reversed by genetic rescue with NT5E cDNA or treatment with exogenous adenosine.

The role of adenosine in inhibiting default calcification in vascular endothelial cells is a new concept that could have an enormous influence on our understanding of ectopic calcification in general. The pathway might also have implications for other specific disorders, including Monckeberg’s medial sclerosis and pseudoxanthoma elasticum (Markello et al., 2011). In addition, knowledge of the basic defect in ACDC allows for consideration of treatment for affected individuals; besides the five siblings described above, four other ACDC patients have been ascertained worldwide, and still more have come to our attention recently. Treatment with bisphosphonates (inhibitors of alkaline phosphatase) is a potential therapy; therefore, we have initiated a clinical protocol to test this.

Novel mutation, unique phenotype

A second example of disease discovery emanating from the NIH UDP focused on a novel spastic ataxia-neuropathy syndrome in two brothers (Pierson et al., 2011). Phenotyping revealed spasticity, peripheral neuropathy, cerebellar ataxia, oculomotor apraxia, dystonia and myoclonic epilepsy. One of the brothers died at age 13; the other was deteriorating at age 14.

Again, consanguinity was involved, but this time in the form of a first cousin marriage. Whereas third cousins share 1/128 of their genes, first cousins share 1/8 of their genes, meaning that more than 10% of the human genome would be homozygous on SNP array analysis. As a consequence, SNP arrays would yield too many candidate genes to guess which ones would warrant further pursuit. Rather, WES was employed to identify genes containing homozygous variants. WES involves massively parallel sequencing of ∼40 million bases that constitute the <2% of the human genome (3.2 billion bases) encoding genes. Using a whole exome platform, not every gene is perfectly sequenced (i.e. ‘covered’), but the breadth is so great that there is a good chance of detecting a causative variant. The problem is that non-pathogenic variants abound, so the exome sequences of other family members are required to reduce (‘filter’) the total number of variants. In the case of the two brothers, a total of 120,469 variants were identified among the two parents and two affected brothers; this was reduced to 59,482 variants not found in the 1000 Genomes database. Of these, 11 were homozygous and, of the 11, three were not present in dbSNP, a database of known polymorphisms. One homozygous missense mutation (c.1847G>A; p.Y616C) in the AFG3L2 gene was identified as the best candidate. AFG3L2 encodes a subunit of a mitochondrial AAA protease that removes damaged or misfolded proteins (Koppen et al., 2007).

As in the case of ACDC, we had a phenotype and a gene, but needed scientific expertise to demonstrate a functional deficit and a mechanism of disease. In this case, Thomas Langer and Elena Rugarli of the University of Cologne in Germany provided the basic research knowledge by using a yeast expression system to study AFG3L2. It was known that AFG3L2 protein forms either a homo-oligomeric isoenzyme or a hetero-oligomeric complex with paraplegin. Langer’s group used yeast complementation assays to show that the mutant (Y616C) AFG3L2 protein is a hypomorphic variant with an impaired ability to form complexes with either itself or with paraplegin (Pierson et al., 2011). This finding was well aligned with the clinical phenotype, because paraplegin was mutated in hereditary spastic paraplegia type 7 (SPG7), and heterozygous AFG3L2 mutations caused autosomal dominant spinocerebellar ataxia type 28 (SCA28) (Atorino et al., 2003; Koppen et al., 2007). The specific homozygous Y616C mutation in our patients produced a unique combination of the phenotypes of SPG7 and SCA28, along with other mitochondrial disease features such as oculomotor apraxia, extrapyramidal dysfunction and myoclonic epilepsy. This new disease discovery significantly broadened the phenotypes associated with both spinocerebellar ataxia and hereditary spastic paraplegia for the neurological community.


The above examples employed a wide range of research modalities – including cutting-edge medical procedures, state-of-the-art genetics, appropriate cell culture systems and model organisms – to come to a final diagnosis. The NIH UDP has many other cases similar to those mentioned above, at different stages of maturation, as well as examples of extremely rare, known diseases. Representative disorders include congenital disorder of glycosylation IIb (De Praeter et al., 2000) being investigated by immunologists, follicular hyperkeratosis being pursued by cell cycle experts and an autosomal dominant myopathy being studied by cell biologists. In every case, genetics ties the clinical investigator to the basic scientist, but some investigations lie fallow for want of bench researchers or experts in the disease. As our knowledge and data in genetics burgeon, we must engage the cognoscenti in a wide variety of fields to discover new diseases, new mechanisms of action and, ultimately, new therapeutic interventions. Only a union of clinical and basic researchers – and an awareness of the rich resource that lies in the population of rare disease patients – can achieve this. We hope that the UDP can serve as a model for similar programs at major medical centers throughout the world.

Atorino L.,Silvestri L.,Koppen M.,Cassina L.,Ballabio A.,Marconi R.,Langer T.,Casari G.. (Year: 2003). Loss of m-AAA protease in mitochondria causes complex I deficiency and increased sensitivity to oxidative stress in hereditary spastic paraplegia. J. Cell Biol.163, 777–78714623864
De Praeter C. M.,Gerwig G. J.,Bause E.,Nuytinck L. K.,Vliegenthart J. F. G.,Breuer W.,Kamerling J. P.,Espeel M. F.,Martin J. J,De Paepe A. M.,et al. (Year: 2000). A novel disorder caused by defective biosynthesis of N-linked oligosaccharides due to glucosidase I deficiency. Am. J. Hum. Genet.66, 1744–175610788335
Gahl W. A.,Tifft C. J.. (Year: 2011). The NIH Undiagnosed Diseases Program: lessons learned. JAMA305, 1904–190521558523
Gahl W. A.,Markello T. C.,Toro C.,Fuentes Fajardo K.,Sincan M.,Gill F.,Carlson-Donohoe H.,Gropman A.,Pierson T. M.,Golas G.,et al. (Year: 2011). The NIH Undiagnosed Diseases Program: insights into rare diseases. Genet. Medicine (in press).
Koppen M.,Metodiev M. D.,Casari G.,Rugarli E. I.,Langer T.. (Year: 2007). Variable and tissue-specific subunit composition of mitochondrial m-AAA protease complexes linked to hereditary spastic paraplegia. Mol. Cell. Biol.27, 758–76717101804
Markello T. C.,Pak L. K.,St. Hilaire C.,Dorward H.,Ziegler S. G.,Chen M. Y.,Chaganti K.,Nussbaum R. L.,Boehm M.,Gahl W. A.. (Year: 2011). Vascular pathology of medial arterial calcifications in NT5E deficiency: implications for the role of adenosine in pseudoxanthoma elasticum. Mol. Genet. Metab.103, 44–5021371928
Pierson T. M.,Adams D.,Bonn F.,Martinelli P.,Cherukuri P. F.,Teer J. K.,Hansen N. F.,Cruz P.,Mullikin J. C.,Blakesley R. W.,et al. (Year: 2011). Whole-exome sequencing identifies homozygous AFG3L2 mutations in a spastic ataxia-neuropathy syndrome linked to mitochondrial m-AAA proteases. PLoS Genetics7, e100232522022284
St. Hilaire C.,Ziegler S. G.,Markello T.,Brusco A.,Groden C.,Gill F.,Carlson-Donohoe H.,Lederman R. J.,Chen M. Y.,Yang D.,et al. (Year: 2011). NT5E mutations and arterial calcifications. N. Engl. J. Med.364, 432–44221288095

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