Evidence map›Paper›PMID 30134969›Full record

ArticleBMC health services research2018

Characteristics of undiagnosed diseases network applicants: implications for referring providers.

Nicole M Walley, Loren D M Pena, Stephen R Hooper, Heidi Cope, Yong-Hui Jiang, Allyn McConkie-Rosell, Camilla Sanders, Kelly Schoch, Rebecca C Spillmann, Kimberly Strong and 7 more

Registry-linked trialAbstract read
In one paragraph

Article in BMC health services research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02450851 (Clinical and Genetic Evaluation of Patients With Undiagnosed Disorders Through the Undiagnosed Diseases Network), which is not on this map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02450851 recruitingnot on this map

Clinical and Genetic Evaluation of Patients With Undiagnosed Disorders Through the Undiagnosed Diseases Network

TypeobservationalSponsorNational Human Genome Research Institute (NHGRI)Ran2015 to 2028Enrolled20,000ConditionsGenetic Disease
3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Equity-focused implementation to enhance access to rare disease genomic research and understand diverse perspectives.Genetics in medicine : official journal of the American College of Medical Genetics · 2026
    Article
  5. Article
  6. Review
  7. The Brain Gene Registry: a data snapshot.Journal of neurodevelopmental disorders · 2024
    Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Observational
  15. Patients as Partners in Rare Disease Diagnosis and Research.The Yale journal of biology and medicine · 2021
    Review
  16. Article
  17. Review
  18. The undiagnosed diseases program: Approach to diagnosis.Translational science of rare diseases · 2020
    Article
  19. Epigenetic Inheritance Underlying Pulmonary Arterial Hypertension.Arteriosclerosis, thrombosis, and vascular biology · 2019
    Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Nicole M WalleyDivision of Medical Genetics, Department of Pediatrics, Duke Health, Box 103857, Durham, NC, 27710, USA.
Loren D M PenaDivision of Medical Genetics, Department of Pediatrics, Duke Health, Box 103857, Durham, NC, 27710, USA.
Stephen R HooperDepartment of Allied Health, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Heidi CopeDivision of Medical Genetics, Department of Pediatrics, Duke Health, Box 103857, Durham, NC, 27710, USA.
Yong-Hui JiangDivision of Medical Genetics, Department of Pediatrics, Duke Health, Box 103857, Durham, NC, 27710, USA.
Allyn McConkie-RosellDivision of Medical Genetics, Department of Pediatrics, Duke Health, Box 103857, Durham, NC, 27710, USA.
Camilla SandersDivision of Medical Genetics, Department of Pediatrics, Duke Health, Box 103857, Durham, NC, 27710, USA.
Kelly SchochDivision of Medical Genetics, Department of Pediatrics, Duke Health, Box 103857, Durham, NC, 27710, USA.
Rebecca C SpillmannDivision of Medical Genetics, Department of Pediatrics, Duke Health, Box 103857, Durham, NC, 27710, USA.
Kimberly StrongEthics and Genomics Program, HudsonAlpha Institute for Biotechnology, Huntsville, AL, USA.
Alexa T McCrayDepartment of Biomedical Informatics, Harvard Medical School, Boston, MA, USA.
Paul MazurDepartment of Biomedical Informatics, Harvard Medical School, Boston, MA, USA.
Cecilia EstevesDepartment of Biomedical Informatics, Harvard Medical School, Boston, MA, USA.
Kimberly LeBlancDepartment of Biomedical Informatics, Harvard Medical School, Boston, MA, USA.
Undiagnosed Diseases Network
Anastasia L WiseNational Human Genome Research Institute, NIH, Bethesda, MD, USA.
Vandana ShashiDivision of Medical Genetics, Department of Pediatrics, Duke Health, Box 103857, Durham, NC, 27710, USA. vandana.shashi@duke.edu.

Funding

Coordinating Center for the Undiagnosed Diseases NetworkU01HG007530 · NHGRI · HARVARD MEDICAL SCHOOL · PI KOHANE, ISAAC S. · 2014 to 2022
$30.2M
An integrated and diverse genomic medicine program for undiagnosed diseasesU01HG007672 · NHGRI · DUKE UNIVERSITY · PI SHASHI, VANDANA · 2014 to 2022
$13.4M
Genomic medicine and gene function implementation for an underserved populationR01HG011795 · NHGRI · BAYLOR COLLEGE OF MEDICINE · PI BELLEN, HUGO J, WANGLER, MICHAEL FRANCIS · 2021 to 2025
$4.8M
Clinical Genome Wide Sequencing Core for the Undiagnosed Disease NetworkU01HG007943 · NHGRI · MEDICAL COLLEGE OF WISCONSIN · PI WORTHEY, ELIZABETH A · 2014 to 2017
$4.1M
NHGRI NIH HHS R01 HG011795NHGRI NIH HHS U01 HG007530NHGRI NIH HHS U01 HG007672NHGRI NIH HHS U01 HG007943
6 · The paper itself

Abstract

backgroundThe majority of undiagnosed diseases manifest with objective findings that warrant further investigation. The Undiagnosed Diseases Network (UDN) receives applications from patients whose symptoms and signs have been intractable to diagnosis; however, many UDN applicants are affected primarily by subjective symptoms such as pain and fatigue. We sought to characterize presenting symptoms, referral sources, and demographic factors of applicants to the UDN to identify factors that may determine application outcome and potentially differentiate between those with undiagnosed diseases (with more objective findings) and those who are less likely to have an undiagnosed disease (more subjective symptoms).

methodsWe used a systematic retrospective review of 151 consecutive Not Accepted and 50 randomly selected Accepted UDN applications. The primary outcome was whether an applicant was Accepted, or Not Accepted, and, if accepted, whether or not a diagnosis was made. Objective and subjective symptoms and information on prior specialty consultations were collected from provider referral letters. Demographic data and decision data on network acceptance were gathered from the UDN online portal.

resultsFewer objective findings and more subjective symptoms were found in the Not Accepted applications. Not Accepted referrals also were from older individuals, reported a shorter period of illness, and were referred to the UDN by their primary care physicians. All of these differences reached statistical significance in comparison with Accepted applications. The frequency of subspecialty consults for diagnostic purposes prior to UDN application was similar in both groups.

conclusionsThe preponderance of subjective and lack of objective findings in the Not Accepted applications distinguish these from applicants that are accepted for evaluation and diagnostic efforts through the UDN. Not Accepted applicants are referred primarily by their primary care providers after multiple specialist consultations fail to yield answers. Distinguishing between patients with undiagnosed diseases with objective findings and those with primarily subjective findings can delineate patients who would benefit from further diagnostic processes from those who may have functional disorders and need alternative pathways for management of their symptoms.

trial registrationclinicaltrials.gov NCT02450851 , posted May 21st 2015.

Indexed as

Disease ManagementAdolescentAdultDecision MakingFemaleGovernment ProgramsHumansMaleMiddle AgedNational Institutes of Health (U.S.)Rare DiseasesReferral and ConsultationRetrospective StudiesUnited StatesYoung AdultGenomicsHealth policyMedically unexplained physical symptomsMedically unexplained symptomsUndiagnosed diseases

Identifiers

PMID30134969
PMCPMC6106923

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.