Evidence map›Paper›PMID 36604708›Full record

ArticleNutrition & metabolism2023

Gut microbiome and stages of diabetes in middle-aged adults: CARDIA microbiome study.

Yi-Han Hu, Katie Meyer, Anju Lulla, Cora E Lewis, Mercedes R Carnethon, Pamela J Schreiner, Stephen Sidney, James M Shikany, Osorio Meirelles, Lenore J Launer

Open access · goldAbstract read
In one paragraph

Article in Nutrition & metabolism, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

15 citing papers in PubMed, 21 citations in OpenAlex.

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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

10 authors at 6 institutions in 1 country.

Yi-Han HuLaboratory of Epidemiology and Population Sciences, National Institute On Aging, 251 Bayview Blvd, Baltimore, MD, 21224, USA.
Katie MeyerNutrition Research Institute, University of North Carolina at Chapel Hill, Kannapolis, NC, USA.
Anju LullaNutrition Research Institute, University of North Carolina at Chapel Hill, Kannapolis, NC, USA.
Cora E LewisDepartment of Epidemiology, University of Alabama at Birmingham, Birmingham, AL, USA.
Mercedes R CarnethonDepartment of Preventive Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Pamela J SchreinerDivision of Epidemiology and Community Health, University of Minnesota, Minneapolis, MN, USA.
Stephen SidneyKaiser Permanente Medical Center Program, Oakland, CA, USA.
James M ShikanyDivision of Preventive Medicine, School of Medicine, University of Alabama at Birmingham, Birmingham, AL, USA.
Osorio MeirellesLaboratory of Epidemiology and Population Sciences, National Institute On Aging, 251 Bayview Blvd, Baltimore, MD, 21224, USA.
Lenore J LaunerLaboratory of Epidemiology and Population Sciences, National Institute On Aging, 251 Bayview Blvd, Baltimore, MD, 21224, USA. launerl@nia.nih.gov.
National Institute on Aging · USDavid H. Murdock Research Institute · USUniversity of Alabama at Birmingham · USKaiser Permanente Oakland Medical Center · USNorthwestern University · USUniversity of Minnesota · US

Funding

University of Alabama at Birmingham's Diabetes Research CenterP30DK079626 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Kirk Michael Habegger · 2013 to 2026
$19.5M
A Novel Gut Microbial-Dependent Nutrient Metabolite and AtherosclerosisK01HL127159 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI MEYER, KATIE A · 2015 to 2019
$787k
NHLBI NIH HHS HHSN268201800004INHLBI NIH HHS HHSN268201800005INHLBI NIH HHS HHSN268201800006INHLBI NIH HHS HHSN268201800007INHLBI NIH HHS K01 HL127159NIDDK NIH HHS P30 DK079626
6 · The paper itself

Abstract

backgroundAnimal and human studies suggest the gut microbiome is linked to diabetes but additional data are needed on the associations of the gut microbiome to specific diabetes characteristics. The aim of this study was to examine the associations of gut microbiome composition to insulin resistance [Homeostatic Model Assessment of Insulin Resistance (HOMA-IR)], duration of diabetes, and 4 stages of diabetes [normoglycemia, pre-diabetes, and diabetes with (+) and without (-) medication for diabetes].

methodsData are from a sub-sample (n = 605) of Black and White participants from the 30-year follow-up exam of the prospectively followed community-based Coronary Artery Risk Development in Young Adults cohort (2015-2016; aged 48-60 years). Stool samples were collected and sequenced using the 16S ribosomal RNA method. Microbial measures included: α diversity (within-person), β diversity (between-person), and taxonomies. All analyses were adjusted for demographic, clinical, lifestyle factors, and use of relevant medications (full adjustment). Multivariate linear regression models were used to assess the association of diabetes characteristics with α diversity and genera abundance, while the association with β diversity was analyzed using permutational multivariate analysis of variance. Statistical significance was set to p-value < 0.05 for α and β diversity analyses and to q-value < 0.1 for genera abundance analyses.

resultsThere were 16.7% of participants with pre-diabetes, and 14.4% with diabetes (9% diabetes+) with median (interquartile range) diabetes duration of 5 (5-10) years. In the fully adjusted models, compared to those with no diabetes, longer diabetes duration and the diabetes + group had a lower α diversity. There were significant differences in β diversity across diabetes-related characteristics. A significantly reduced abundance of butyrate-producing genera was associated with higher HOMA-IR (ex., Anaerostipes and Lachnospiraceae_UCG.004), longer diabetes duration (ex., Agathobacter and Ruminococcus), and diabetes + (ex., Faecalibacterium and Romboutsia).

conclusionsOur results suggest that an adverse alteration of gut microbiome composition is related to higher insulin resistance, longer diabetes duration, and is present in those persons with diabetes using medications. These diabetes-related characteristics were also associated with lower levels of certain butyrate-producing bacteria that produce health-promoting short-chain fatty acids. Understanding the role of gut microbiota in glucose regulation may provide new strategies to reduce the burden of diabetes.

Indexed as

DiabetesDiabetes durationGut microbiota compositionInsulin resistancePopulation-based

Identifiers

PMID36604708
PMCPMC9817375
OpenAlexW4313561298

What OpenQuestion holds

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LicenceCC BY
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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.