Evidence map›Paper›PMID 27066308›Full record

ArticleBrain and behavior2016

Dopamine pathway gene variants may modulate cognitive performance in the DHS - Mind Study.

Susan E Martelle, Laura M Raffield, Nichole D Palmer, Amanda J Cox, Barry I Freedman, Christina E Hugenschmidt, Jeff D Williamson, Don W Bowden

Open access · goldAbstract read
In one paragraph

Article in Brain and behavior, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Parkinson disease-associated cognitive impairment.Nature reviews. Disease primers · 2021
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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

8 authors at 2 institutions in 2 countries.

Susan E MartelleDepartment of Physiology and Pharmacology Wake Forest School of Medicine Winston - Salem North Carolina; Center for Genomics and Personalized Medicine Research Wake Forest School of Medicine Winston - Salem North Carolina.
Laura M RaffieldCenter for Genomics and Personalized Medicine Research Wake Forest School of Medicine Winston - Salem North Carolina.
Nichole D PalmerCenter for Genomics and Personalized Medicine Research Wake Forest School of Medicine Winston - Salem North Carolina.
Amanda J CoxMolecular Basis of Disease Griffith University Southport Brisbane Queensland Australia.
Barry I FreedmanDepartment of Internal Medicine, Nephrology Wake Forest School of Medicine Winston - Salem North Carolina.
Christina E HugenschmidtDepartment of Internal Medicine, Gerontology and Geriatric Medicine Wake Forest School of Medicine Winston - Salem North Carolina.
Jeff D WilliamsonDepartment of Internal Medicine, Gerontology and Geriatric Medicine Wake Forest School of Medicine Winston - Salem North Carolina.
Don W BowdenCenter for Genomics and Personalized Medicine Research Wake Forest School of Medicine Winston - Salem North Carolina.
Wake Forest University · USGriffith University · AU

Funding

Epidemiology of cardiovascular disease in diabetesR01HL067348 · NHLBI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI BOWDEN, DONALD W · 2001 to 2004
$4.3M
Genetic Epidemiology of Cerebrovascular Disease and Cognition in DiabetesR01NS058700 · NINDS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI BOWDEN, DONALD W · 2008 to 2012
$3.0M
Whole Genome Association Analysis of the Diabetes Heart StudyR01HL092301 · NHLBI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI BOWDEN, DONALD W · 2010 to 2013
$2.7M
Cognitive/Brain Effects of Adding Weight Loss to Exercise in Obese Older AdultsK01AG043547 · NIA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI HUGENSCHMIDT, CHRISTINA E · 2013 to 2017
$609k
Genetic and imaging analysis of cerebrovascular disease and cognition in diabetesF32DK083214 · NIDDK · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI HUGENSCHMIDT, CHRISTINA E · 2008 to 2011
$157k
Analysis of Coding Variants Associated with Age-Related PhenotypesF31AG044879 · NIA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI RAFFIELD, LAURA M · 2013 to 2015
$86k
NHLBI NIH HHS R01 HL067348NHLBI NIH HHS R01 HL092301NIA NIH HHS F31 AG044879NIA NIH HHS K01 AG043547NIDDK NIH HHS F32 DK083214NINDS NIH HHS R01 NS058700
6 · The paper itself

Abstract

backgroundThere is an established association between type 2 diabetes and accelerated cognitive decline. The exact mechanism linking type 2 diabetes and reduced cognitive function is less clear. The monoamine system, which is extensively involved in cognition, can be altered by type 2 diabetes status. Thus, this study hypothesized that sequence variants in genes linked to dopamine metabolism and associated pathways are associated with cognitive function as assessed by the Digit Symbol Substitution Task, the Modified Mini-Mental State Examination, the Stroop Task, the Rey Auditory-Verbal Learning Task, and the Controlled Oral Word Association Task for Phonemic and Semantic Fluency in the Diabetes Heart Study, a type 2 diabetes-enriched familial cohort (n = 893).

methodsTo determine the effects of candidate variants on cognitive performance, genetic association analyses were performed on the well-documented variable number tandem repeat located in the 3' untranslated region of the dopamine transporter, as well as on single-nucleotide polymorphisms covering genes in the dopaminergic pathway, the insulin signaling pathway, and the convergence of both. Next, polymorphisms in loci of interest with strong evidence for involvement in dopamine processing were extracted from genetic datasets available in a subset of the cohort (n = 572) derived from Affymetrix(®) Genome-Wide Human SNP Array 5.0 and 1000 Genomes imputation from this array.

resultsThe candidate gene analysis revealed one variant from the DOPA decarboxylase gene, rs10499695, to be associated with poorer performance on a subset of Rey Auditory-Verbal Learning Task measuring retroactive interference (P = 0.001, β = -0.45). Secondary analysis of genome-wide and imputed data uncovered another DOPA decarboxylase variant, rs62445903, also associated with retroactive interference (P = 7.21 × 10(-7), β = 0.3). These data suggest a role for dopaminergic genes, specifically a gene involved in regulation of dopamine synthesis, in cognitive performance in type 2 diabetes.

Indexed as

Genome-Wide Association StudyAdultAgedAged, 80 and overAromatic-L-Amino-Acid DecarboxylasesCognitive DysfunctionCohort StudiesDiabetes Mellitus, Type 2DopamineDopamine Plasma Membrane Transport ProteinsFemaleHumansMaleMiddle AgedMinisatellite RepeatsPedigreeAromatic-L-Amino-Acid DecarboxylasesDDC protein, humanDopamineDopamine Plasma Membrane Transport ProteinsSLC6A3 protein, humanCognitionDAT1 VNTRDOPA decarboxylasedopaminepolymorphismtype 2 diabetes

Identifiers

PMID27066308
PMCPMC4797918
OpenAlexW2334787884

What OpenQuestion holds

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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.