Evidence map›Paper›PMID 27665271›Full record

ReviewMolecular genetics and metabolism2016

Nutritional interventions in primary mitochondrial disorders: Developing an evidence base.

Kathryn M Camp, Danuta Krotoski, Melissa A Parisi, Katrina A Gwinn, Bruce H Cohen, Christine S Cox, Gregory M Enns, Marni J Falk, Amy C Goldstein, Rashmi Gopal-Srivastava and 19 more

Open access · greenAbstract readReview
In one paragraph

Review in Molecular genetics and metabolism, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
3.5field-weighted citation impact, top 7% of its field
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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 59 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Advances in Management of Mitochondrial Myopathies.International journal of molecular sciences · 2025
    Review
  4. Article
  5. Metabolomic changes in children with autism.World journal of clinical pediatrics · 2024
    Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. Therapy Prospects for Mitochondrial DNA Maintenance Disorders.International journal of molecular sciences · 2021
    Review
  11. Review
  12. Review
  13. Overview of Atypical Diabetes.Endocrinology and metabolism clinics of North America · 2020
    Review
  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Towards a therapy for mitochondrial disease: an update.Biochemical Society transactions · 2018
    Review
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

29 authors at 19 institutions in 4 countries.

Kathryn M CampOffice of Dietary Supplements, National Institutes of Health, Bethesda, MD 20892, USA. Electronic address: campkm@od.nih.gov.
Danuta KrotoskiEunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA. Electronic address: krotoskd@mail.nih.gov.
Melissa A ParisiEunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA. Electronic address: parisima@mail.nih.gov.
Katrina A GwinnNational Institute of Neurological Diseases and Stroke, National Institutes of Health, Bethesda, MD 20892, USA. Electronic address: gwinnk@ninds.nih.gov.
Bruce H CohenDepartment of Pediatrics, Akron Children's Hospital, Akron, OH 44308, USA. Electronic address: bcohen@chmca.org.
Christine S CoxMitoAction, Boston, MA 02205, USA. Electronic address: outreach@mitoaction.org.
Gregory M EnnsDivision of Medical Genetics, Stanford University, Stanford, CA 94305, USA. Electronic address: genns@stanford.edu.
Marni J FalkThe Children's Hospital of Philadelphia and University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104, USA. Electronic address: falkm@email.chop.edu.
Amy C GoldsteinDivision of Child Neurology, Children's Hospital of Pittsburgh, Pittsburgh, PA 15224, USA. Electronic address: amy.goldstein@chp.edu.
Rashmi Gopal-SrivastavaNational Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, MD 20892, USA. Electronic address: rashmi.gopal-srivastava@nih.gov.
Gráinne S GormanWellcome Trust Centre for Mitochondrial Research, Newcastle University, Newcastle upon Tyne NE2 4HH, UK. Electronic address: grainne.gorman@newcastle.ac.uk.
Stephen P HershJ. Willard & Alice S. Marriott Foundation, Bethesda, MD 20817, USA. Electronic address: hershs@starpower.net.
Michio HiranoColumbia University Medical Center, New York, NY 10032, USA. Electronic address: mh29@cumc.columbia.edu.
Freddie Ann HoffmanHeteroGeneity, LLC, Washington, DC 20011, USA. Electronic address: fhoffman@heterogeneity-LLC.com.
Amel KaraaGenetics Unit, Massachusetts General Hospital, Boston, MA 02114, USA. Electronic address: akaraa@mgh.harvard.edu.
Erin L MacLeodDivision of Genetics and Metabolism, Children's National Health System, Washington, DC 20010, USA. Electronic address: emacleod@childrensnational.org.
Robert McFarlandWellcome Trust Centre for Mitochondrial Research, Newcastle University, Newcastle upon Tyne NE2 4HH, UK. Electronic address: robert.mcfarland@newcastle.ac.uk.
Charles MohanUnited Mitochondrial Disease Foundation, Pittsburgh, PA 15239, USA. Electronic address: chuckm@umdf.org.
Andrew E MulbergCenter for Drug Evaluation and Research, Food and Drug Administration, Silver Spring, MD 20903, USA. Electronic address: amulberg@amicusrx.com.
Joanne C OdenkirchenNational Institute of Neurological Diseases and Stroke, National Institutes of Health, Bethesda, MD 20892, USA. Electronic address: jo21x@nih.gov.
Sumit ParikhNeurosciences, Cleveland Clinic, Cleveland, OH 44195, USA. Electronic address: parikhs@ccf.org.
Patricia J RutherfordVitaflo International Ltd, Liverpool L34BQ, UK. Electronic address: triciarutherford@vitaflo.co.uk.
Shawne K Suggs-AndersonOffice of Nutrition and Food Labeling, Food and Drug Administration, College Park, MD 20740, USA. Electronic address: shawne.suggs-anderson@fda.hhs.gov.
W H Wilson TangCenter for Clinical Genomics, Cleveland Clinic, Cleveland, OH 44195, USA. Electronic address: tangw@ccf.org.
Jerry VockleyUniversity of Pittsburgh School of Medicine, Pittsburgh, PA 15224, USA. Electronic address: gerard.vockley@chp.edu.
Lynne A WolfeNational Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA. Electronic address: lynne.wolfe@nih.gov.
Steven YannicelliMedical and Scientific Affairs, Nutricia North America, Rockville, MD 20850, USA. Electronic address: steven.yannicelli@nutricia.com.
Philip E YeskeUnited Mitochondrial Disease Foundation, Pittsburgh, PA 15239, USA. Electronic address: philip.yeske@umdf.org.
Paul M CoatesOffice of Dietary Supplements, National Institutes of Health, Bethesda, MD 20892, USA. Electronic address: coatesp@od.nih.gov.
National Institutes of Health · USCleveland Clinic · USUnited Mitochondrial Disease Foundation · USWellcome Centre for Mitochondrial Research · GBAkron Children's Hospital · USCenter for Drug Evaluation and Research · USCenter for Food Safety and Applied Nutrition · USChildren's Hospital of Philadelphia · USChildren's Hospital of Pittsburgh · USChildren's National · USColumbia University Irving Medical Center · USFoundation for the National Institutes of Health · USHess (United States) · USMassachusetts General Hospital · USMitre (United States) · USNutricia Research (Netherlands) · NLStanford Medicine · USUniversity of Pittsburgh · USVitalograph (Ireland) · IE

Funding

Pharmacologic Treatment of Mitochondrial Complex I Dysfunction in C. ElegansR01GM120762 · NIGMS · CHILDREN'S HOSP OF PHILADELPHIA · PI FALK, MARNI J · 2016 to 2019
$2.4M
Intramural NIH HHS Z99 OD999999NIGMS NIH HHS R01 GM120762Wellcome Trust
6 · The paper itself

Abstract

In December 2014, a workshop entitled "Nutritional Interventions in Primary Mitochondrial Disorders: Developing an Evidence Base" was convened at the NIH with the goals of exploring the use of nutritional interventions in primary mitochondrial disorders (PMD) and identifying knowledge gaps regarding their safety and efficacy; identifying research opportunities; and forging collaborations among researchers, clinicians, patient advocacy groups, and federal partners. Sponsors included the NIH, the Wellcome Trust, and the United Mitochondrial Diseases Foundation. Dietary supplements have historically been used in the management of PMD due to their potential benefits and perceived low risk, even though little evidence exists regarding their effectiveness. PMD are rare and clinically, phenotypically, and genetically heterogeneous. Thus patient recruitment for randomized controlled trials (RCTs) has proven to be challenging. Only a few RCTs examining dietary supplements, singly or in combination with other vitamins and cofactors, are reported in the literature. Regulatory issues pertaining to the use of dietary supplements as treatment modalities further complicate the research and patient access landscape. As a preface to exploring a research agenda, the workshop included presentations and discussions on what PMD are; how nutritional interventions are used in PMD; challenges and barriers to their use; new technologies and approaches to diagnosis and treatment; research opportunities and resources; and perspectives from patient advocacy, industry, and professional organizations. Seven key areas were identified during the workshop. These areas were: 1) defining the disease, 2) clinical trial design, 3) biomarker selection, 4) mechanistic approaches, 5) challenges in using dietary supplements, 6) standards of clinical care, and 7) collaboration issues. Short- and long-term goals within each of these areas were identified. An example of an overarching goal is the enrollment of all individuals with PMD in a natural history study and a patient registry to enhance research capability. The workshop demonstrates an effective model for fostering and enhancing collaborations among NIH and basic research, clinical, patient, pharmaceutical industry, and regulatory stakeholders in the mitochondrial disease community to address research challenges on the use of dietary supplements in PMD.

Indexed as

Dietary SupplementsNutritional StatusHumansMitochondriaMitochondrial DiseasesVitaminsVitaminsDietary supplementsMedical foodsMitochondrial diseaseNutritional interventionsOXPHOSPrimary mitochondrial disorders

Identifiers

PMID27665271
PMCPMC5083179
OpenAlexW2522036428

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.