Evidence map›Paper›PMID 21788574›Full record

ArticleDiabetes2011

Does genetic ancestry explain higher values of glycated hemoglobin in African Americans?

Nisa M Maruthur, W H Linda Kao, Jeanne M Clark, Frederick L Brancati, Ching-Yu Cheng, James S Pankow, Elizabeth Selvin

Open access · hybridAbstract read
In one paragraph

Article in Diabetes, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 3 pooled it
4.4field-weighted citation impact, top 5% 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

26 citing papers in PubMed, 3 syntheses or guidelines pooled it, 45 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Trial
  6. Misuse of Race in the Interpretation of HbAAnnals of internal medicine · 2025
    Article
  7. Article
  8. HbAPreventing chronic disease · 2021
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  17. Differing effects of metformin on glycemic control by race-ethnicity.The Journal of clinical endocrinology and metabolism · 2014
    Article
  18. Article
  19. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 2 countries.

Nisa M MaruthurDivision of General Internal Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
W H Linda Kao
Jeanne M Clark
Frederick L Brancati
Ching-Yu Cheng
James S Pankow
Elizabeth Selvin
Johns Hopkins Medicine · USJohns Hopkins University · USSingapore Eye Research Institute · SGUniversity of Minnesota · US

Funding

Institute for Clinical and Translational Research (KL2)KL2RR025006 · NCRR · JOHNS HOPKINS UNIVERSITY · PI FORD, DANIEL ERNEST · 2007 to 2011
$12.9M
JHU-UMD Diabetes Research CenterP30DK079637 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI WONDISFORD, FREDRIC E. · 2013 to 2017
$9.7M
GENOTYPING FOR LOCATING HUMAN DISEASE GENESN01HG065403 · NHGRI · JOHNS HOPKINS UNIVERSITY · PI VALLE, DAVID L · 1996 to 2000
$1.7M
Genetic Epidemiology of NAFLD and T2DMK01DK067207 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI KAO, WEN HONG LINDA · 2005 to 2009
$642k
Glycemia Advanced Gylcation End products (AGEs) and Atherosclerosis in DiabetesK01DK076595 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI SELVIN, ELIZABETH · 2006 to 2010
$606k
Admixture Mapping to Identify T2DM Genes in African AmericansR21DK073482 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI KAO, WEN HONG LINDA · 2006 to 2007
$475k
Defining the Clinical Significance of HbA1c Prior to the Onset of DiabetesR21DK080294 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI SELVIN, ELIZABETH · 2007 to 2008
$325k
NCRR NIH HHS 1KL2-RR-025006-01NCRR NIH HHS KL2 RR025006NHGRI NIH HHS N01 HG065403NHLBI NIH HHS HHSN268201100005CNHLBI NIH HHS HHSN268201100005GNHLBI NIH HHS HHSN268201100005INHLBI NIH HHS HHSN268201100006CNHLBI NIH HHS HHSN268201100007CNHLBI NIH HHS HHSN268201100007INHLBI NIH HHS HHSN268201100008CNHLBI NIH HHS HHSN268201100008INHLBI NIH HHS HHSN268201100009CNHLBI NIH HHS HHSN268201100009INHLBI NIH HHS HHSN268201100010CNHLBI NIH HHS HHSN268201100011CNHLBI NIH HHS HHSN268201100011INHLBI NIH HHS HHSN268201100012CNHLBI NIH HHS N01 HV048195NHLBI NIH HHS N01-HV-48195NIDDK NIH HHS K01 DK067207NIDDK NIH HHS K01-DK-067207NIDDK NIH HHS K01 DK076595NIDDK NIH HHS K01-DK-076595NIDDK NIH HHS P30 DK079637NIDDK NIH HHS R21 DK073482NIDDK NIH HHS R21-DK-073482NIDDK NIH HHS R21 DK080294NIDDK NIH HHS R21-DK-080294
6 · The paper itself

Abstract

objectiveGlycated hemoglobin (HbA(1c)) values are higher in African Americans than whites, raising the question of whether classification of diabetes status by HbA(1c) should differ for African Americans. We investigated the relative contribution of genetic ancestry and nongenetic factors to HbA(1c) values and the effect of genetic ancestry on diabetes classification by HbA(1c) in African Americans. RESEARCH DESIGN AND

methodsWe performed a cross-sectional analysis of data from the community-based Atherosclerosis Risk in Communities (ARIC) Study. We estimated percentage of European genetic ancestry (PEA) for each of the 2,294 African Americans without known diabetes using 1,350 ancestry-informative markers. HbA(1c) was measured from whole-blood samples and categorized using American Diabetes Association diagnostic cut points (<5.7, 5.7-6.4, and ≥6.5%).

resultsPEA was inversely correlated with HbA(1c) (adjusted r = -0.07; P < 0.001) but explained <1% of its variance. Age and socioeconomic and metabolic factors, including fasting glucose, explained 13.8% of HbA(1c) variability. Eleven percent of participants were classified as having diabetes; adjustment for fasting glucose decreased this to 4.4%. Additional adjustment for PEA did not significantly reclassify diabetes status (net reclassification index = 0.034; P = 0.94) nor did further adjustment for demographic, socioeconomic, and metabolic risk factors.

conclusionsThe relative contribution of demographic and metabolic factors far outweighs the contribution of genetic ancestry to HbA(1c) values in African Americans. Moreover, the impact of adjusting for genetic ancestry when classifying diabetes by HbA(1c) is minimal after taking into account fasting glucose levels, thus supporting the use of currently recommended HbA(1c) categories for diagnosis of diabetes in African Americans.

Indexed as

Black or African AmericanBlack PeopleBlood GlucoseCross-Sectional StudiesFemaleGlycated HemoglobinHumansMaleMiddle AgedProspective StudiesBlood GlucoseGlycated Hemoglobin

Identifiers

PMID21788574
PMCPMC3161314
OpenAlexW2150873076

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.