Evidence map›Paper›PMID 25394619›Full record

ArticleThe journals of gerontology. Series A, Biological sciences and medical sciences2015

Mitochondrial DNA Sequence Variation Associated With Peripheral Nerve Function in the Elderly.

Shana M Katzman, Elsa S Strotmeyer, Michael A Nalls, Yiqiang Zhao, Sean Mooney, Nik Schork, Anne B Newman, Tamara B Harris, Kristine Yaffe, Steven R Cummings and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in The journals of gerontology. Series A, Biological sciences and medical sciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 2 pooled it
0.3field-weighted citation impact, top 39% 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

6 citing papers in PubMed, 2 syntheses or guidelines pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Joint and Individual Mitochondrial DNA Variation and Cognitive Outcomes in Black and White Older Adults.The journals of gerontology. Series A, Biological sciences and medical sciences · 2024
    Article
  4. Article
  5. Article
  6. 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

13 authors at 5 institutions in 1 country.

Shana M KatzmanDepartment of Innovation, Technology, and Alliances, University of California, San Francisco and.
Elsa S StrotmeyerDepartment of Epidemiology, Graduate School of Public Health, University of Pittsburgh, Pennsylvania and.
Michael A NallsLaboratory of Neurogenetics, Intramural Research Program, National Institute on Aging, Bethesda, Maryland and.
Yiqiang ZhaoState Key Laboratory for Agrobiotechnology, China Agricultural University, Beijing, China and.
Sean MooneyDepartment of Bioinformatics, Buck Institute for Research on Aging, Novato, California and.
Nik SchorkDepartment of Human Biology, J. Craig Venter Institute, La Jolla, California and.
Anne B NewmanDepartment of Epidemiology, Graduate School of Public Health, University of Pittsburgh, Pennsylvania and.
Tamara B HarrisLaboratory of Epidemiology, Demography, and Biometry, National Institute on Aging, Bethesda, Maryland and.
Kristine YaffeDepartments of Psychiatry, Neurology, and Epidemiology, University of California, and Department of Geriatric Psychiatry, San Francisco VA Medical Center and.
Steven R CummingsCalifornia Pacific Medical Center Research Institute, San Francisco and.
Yongmei LiuDivision of Public Health Sciences, Wake Forest School of Medicine, Winston-Salem, North Carolina.
Gregory J TranahCalifornia Pacific Medical Center Research Institute, San Francisco and gtranah@sfcc-cpmc.edu.
Health, Aging, and Body Composition Study
California Pacific Medical Center · USJ. Craig Venter Institute · USNational Institute on Aging · USSan Francisco VA Medical Center · USWake Forest University · US

Funding

Informatic Profiling of Clinically Relevant MutationR01LM009722 · NLM · UNIVERSITY OF WASHINGTON · PI MOONEY, SEAN DAVID · 2007 to 2014
$3.5M
Peripheral Nerve Function Decline in an Aged CohortR01AG028050 · NIA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI STROTMEYER, ELSA S. · 2007 to 2015
$3.5M
Genetic Determinants of Visceral AdiposityR01AG032098 · NIA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI LIU, YONGMEI · 2009 to 2013
$3.4M
End of Life in the Very OldR01NR012459 · NINR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI ALBERT, STEVEN M, LUNNEY, JUNE R · 2011 to 2015
$2.7M
Genetic analysis of AGES-Reykjavik Study and the Health ABCZIAAG006000 · NIA · NATIONAL INSTITUTE ON AGING · PI HARRIS, TAMARA · 2009 to 2017
$1.3M
DYNAMICS OF HEALTH .AGING . AND BODY COMPOSITION /Pittsburgh/-260962101N01AG062101 · NIA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · 1996 to 2004
$996k
DYNAMICS OF HEALTH . AGING . AND BODY COMPOSITION /Memphis/-26062103N01AG062103 · NIA · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · 1996 to 2004
$793k
Mitochondrial DNA Variation in Human Energy Expenditure and Metabolic RateR03AG032498 · NIA · CALIFORNIA PACIFIC MED CTR RES INSTITUTE · PI TRANAH, GREGORY J. · 2009 to 2010
$121k
HEALTH ABC--COORDINATING UNIT /California/-260062106N01AG062106 · NIA · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · 1996 to 2004
$109k
Intramural NIH HHSNIA NIH HHS N01-AG-6-2101NIA NIH HHS N01-AG-6-2103NIA NIH HHS N01-AG-6-2106NIA NIH HHS R01 AG028050NIA NIH HHS R01-AG028050NIA NIH HHS R01-AG032098NIA NIH HHS R03-AG032498NINR NIH HHS R01-NR012459NLM NIH HHS LM009722PHS HHS HHSN268200782096CPHS HHS Z01A6000932
6 · The paper itself

Abstract

backgroundMitochondrial dysfunction is a prominent hallmark of many sensory neuropathies. The purpose of this study was to assess the influence of mitochondrial DNA sequence variation on peripheral nerve function in the population-based Health, Aging, and Body Composition Study.

methodsWe investigated the role of common mitochondrial DNA variation (n = 1,580) and complete mitochondrial DNA sequences (n = 138) on peroneal motor nerve conduction velocity and amplitude, average vibration detection threshold, and monofilament sensitivity.

resultsNominal associations among common mitochondrial DNA variants and haplogroups were identified but were not statistically significant after adjustment for multiple comparisons. Sequence-based approaches were used to identify aggregate variant associations across the 16S rRNA (weighted-sum, p = 2E-05 and variable threshold, p = 9E-06) for nerve conduction velocity. Several of these rare 16S variants occurred at or near sites with earlier disease associations and are also in close proximity to the peptidyl transferase center, which is the catalytic center of the 16S rRNA

conclusionsThese results suggest that sequence variation related to mitochondrial protein synthesis/assembly is associated with peripheral nerve function and may provide insight into targets for intervention or new clinical strategies to preserve nerve function in late life.

Indexed as

AgedBody CompositionCohort StudiesDNA, MitochondrialFemaleGenotypeHumansMaleMutationNeural ConductionPeroneal NerveReaction TimeRNA, Ribosomal, 16SDNA, MitochondrialRNA, Ribosomal, 16SEpidemiologyFunctional Performance.GeneticsSensory

Identifiers

PMID25394619
PMCPMC4612380
OpenAlexW2133829086

What OpenQuestion holds

Textmetadata
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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.