Evidence map›Paper›PMID 24942103›Full record

ArticleDiabetologia2014

Association of African genetic ancestry with fasting glucose and HbA1c levels in non-diabetic individuals: the Boston Area Community Health (BACH) Prediabetes Study.

James B Meigs, Richard W Grant, Rebecca Piccolo, Lenny López, Jose C Florez, Bianca Porneala, Lisa Marceau, John B McKinlay

Open access · bronzeAbstract read
In one paragraph

Article in Diabetologia, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.6field-weighted citation impact, top 15% 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

12 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. HbAPreventing chronic disease · 2021
    Article
  7. Pitfalls of HbA1c in the Diagnosis of Diabetes.The Journal of clinical endocrinology and metabolism · 2020
    Article
  8. Article
  9. Article
  10. Glucose level decline precedes dementia in elderly African Americans with diabetes.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2017
    Article
  11. Article
  12. 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

8 authors at 3 institutions in 1 country.

James B MeigsDivision of General Internal Medicine, Department of Medicine, Massachusetts General Hospital, 50 Staniford St, 9th Floor, Boston, MA, 02114, USA, jmeigs@partners.org.
Richard W Grant
Rebecca Piccolo
Lenny López
Jose C Florez
Bianca Porneala
Lisa Marceau
John B McKinlay
Massachusetts General Hospital · USNew England Research Institutes · USKaiser Permanente · US

Funding

Common Genetic Variation and Quantitative Diabetes TraitsR01DK078616 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI MEIGS, JAMES B · 2008 to 2014
$5.0M
Upstream Contributors to Downstream Disparities in Type 2 Diabetes - A Multi-LeveR01DK080786 · NIDDK · NEW ENGLAND RESEARCH INSTITUTES, INC. · PI MCKINLAY, JOHN B · 2009 to 2013
$3.3M
Epidemiology of Precursors to Type 2 DiabetesK24DK080140 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI MEIGS, JAMES B · 2007 to 2016
$1.9M
Association of Acculturation with Type 2 Diabetes Risk Among US LatinosK23DK098280 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LOPEZ, LENNY · 2013 to 2016
$737k
NIDDK NIH HHS K23 DK098280NIDDK NIH HHS K24 DK080140NIDDK NIH HHS R01 DK078616NIDDK NIH HHS R01 DK080786
6 · The paper itself

Abstract

aims/hypothesisTo test among diabetes-free urban community-dwelling adults the hypothesis that the proportion of African genetic ancestry is positively associated with glycaemia, after accounting for other continental ancestry proportions, BMI and socioeconomic status (SES).

methodsThe Boston Area Community Health cohort is a multi-stage 1:1:1 stratified random sample of self-identified African-American, Hispanic and white adults from three Boston inner city areas. We measured 62 ancestry informative markers, fasting glucose (FG), HbA1c, BMI and SES (income, education, occupation and insurance status) and analysed 1,387 eligible individuals (379 African-American, 411 Hispanic, 597 white) without clinical or biochemical evidence of diabetes. We used three-heritage multinomial linear regression models to test the association of FG or HbA1c with genetic ancestry proportion adjusted for: (1) age and sex; (2) age, sex and BMI; and (3) age, sex, BMI and SES.

resultsMean age- and sex-adjusted FG levels were 5.73 and 5.54 mmol/l among those with 100% African or European ancestry, respectively. Using per cent European ancestry as the referent, each 1% increase in African ancestry proportion was associated with an age- and sex-adjusted FG increase of 0.0019 mmol/l (p = 0.01). In the BMI- and SES-adjusted model the slope was 0.0019 (p = 0.02). Analysis of HbA1c gave similar results. CONCLUSIONS/

interpretationA greater proportion of African genetic ancestry is independently associated with higher FG levels in a non-diabetic community-based cohort, even accounting for other ancestry proportions, obesity and SES. The results suggest that differences between African-Americans and whites in type 2 diabetes risk may include genetically mediated differences in glucose homeostasis.

Indexed as

AdultAgedAged, 80 and overAnimalsBlack or African AmericanBlack PeopleFastingFemaleGlucoseGlycated HemoglobinHumansMaleMiddle AgedPrediabetic StateGlucoseGlycated Hemoglobinhemoglobin A1c protein, human

Identifiers

PMID24942103
PMCPMC5424892
OpenAlexW2046795558

What OpenQuestion holds

Textmetadata
LicenceTDM
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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.