Evidence mapPaperPMID 37426694Full record

ArticleEnvironmental advances2023

Arsenic metabolism, diabetes prevalence, and insulin resistance among Mexican Americans: A mendelian randomization approach.

Margaret C Weiss, Yu-Hsuan Shih, Molly Scannell Bryan, Brian P Jackson, David Aguilar, Eric L Brown, Goo Jun, Craig L Hanis, Maria Argos, Robert M Sargis

Open access · goldAbstract read
In one paragraph

Article in Environmental advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.1field-weighted citation impact, top 26% 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

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
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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 4 institutions in 1 country.

Margaret C WeissSchool of Public Health, University of Illinois at Chicago, Chicago, IL, United States of America.
Yu-Hsuan ShihSchool of Public Health, University of Illinois at Chicago, Chicago, IL, United States of America.
Molly Scannell BryanInstitute for Minority Health Research, University of Illinois at Chicago, United States of America.
Brian P JacksonDepartment of Earth Sciences, Dartmouth College, Hanover, NH, United States of America.
David AguilarDivision of Cardiovascular Medicine, LSU Health School of Medicine, New Orleans, LA, United States.
Eric L BrownCenter for Infectious Disease, University of Texas Health Science Center at Houston, Houston, TX, United States.
Goo JunHuman Genetics Center, University of Texas Health Science Center at Houston, Houston, TX, United States.
Craig L HanisHuman Genetics Center, University of Texas Health Science Center at Houston, Houston, TX, United States.
Maria ArgosSchool of Public Health, University of Illinois at Chicago, Chicago, IL, United States of America.
Robert M SargisCollege of Medicine, University of Illinois at Chicago, Chicago, IL, United States of America.
University of Illinois Chicago · USThe University of Texas Health Science Center at Houston · USDartmouth College · USLouisiana State University Health Sciences Center New Orleans · US

Funding

Translational Engineering in Cancer (TEC)P30CA023108 · NCI · DARTMOUTH COLLEGE · 1985 to 2025
$35.3M
ChicAgo Center for Health and EnvironmenT (CACHET)P30ES027792 · UNIVERSITY OF CHICAGO · 2025 to 2025
$1.6M
Diabetes Progression with Metabolomic Profiling in Starr County Mexican AmericansR01DK118631 · NIDDK · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI Goo Jun · 2023 to 2023
$579k
Selenoproteins in Arsenic-Induced Metabolic DysfunctionR01ES028879 · NIEHS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI Robert M Sargis · 2022 to 2022
$499k
The Impact of Metals and Metal Mixtures on Cardiometabolic Disease Trajectories in Hispanics/LatinosF30ES033510 · UNIVERSITY OF ILLINOIS AT CHICAGO · 2025 to 2025
$55k
NCATS NIH HHS UL1 TR002003NCI NIH HHS P30 CA023108NHLBI NIH HHS R01 HL102830NIDDK NIH HHS R01 DK116378NIDDK NIH HHS R01 DK118631NIEHS NIH HHS F30 ES033510NIEHS NIH HHS P30 ES027792NIEHS NIH HHS R01 ES028879NIEHS NIH HHS R21 ES030884NIGMS NIH HHS T32 GM079086
6 · The paper itself

Abstract

Background: Differences in arsenic metabolism capacity may influence risk for type 2 diabetes, but the mechanistic drivers are unclear. We evaluated the associations between arsenic metabolism with overall diabetes prevalence and with static and dynamic measures of insulin resistance among Mexican Americans living in Starr County, Texas. Methods: We utilized data from cross-sectional studies conducted in Starr County, Texas, from 2010-2014. A Mendelian randomization approach was utilized to evaluate the associations between arsenic metabolism and type 2 diabetes prevalence using the intronic variant in the arsenic methylating gene, rs9527, as the instrumental variable for arsenic metabolism. To further assess mechanisms for diabetes pathogenesis, proportions of the urinary arsenic metabolites were employed to assess the association between arsenic metabolism and insulin resistance among participants without diabetes. Urinary biomarkers of arsenic metabolites were modeled as individual proportions of the total. Arsenic metabolism was evaluated both with a static outcome of insulin resistance, homeostatic measure of assessment (HOMA-IR), and a dynamic measure of insulin sensitivity, Matsuda Index. Results: Among 475 Mexican American participants from Starr County, higher metabolism capacity for arsenic is associated with higher diabetes prevalence driven by worse insulin resistance. Presence of the minor T allele of rs9527 is independently associated with an increase in the proportion of monomethylated arsenic (MMA%) and is associated with an odds ratio of 0.50 (95% CI: 0.24, 0.90) for type 2 diabetes. This association was conserved after potential covariate adjustment. Furthermore, among participants without type 2 diabetes, the highest quartile of MMA% was associated with 22% (95% CI: -33.5%, -9.07%) lower HOMA-IR and 56% (95% CI: 28.3%, 91.3%) higher Matsuda Index for insulin sensitivity. Conclusions: Arsenic metabolism capacity, indicated by a lower proportion of monomethylated arsenic, is associated with increased diabetes prevalence driven by an insulin resistant phenotype among Mexican Americans living in Starr County, Texas.

Indexed as

ArsenicEndocrine disruptorInsulin resistanceInsulin sensitivityMethylationType 2 diabetes

Identifiers

PMID37426694
PMCPMC10328543
OpenAlexW4360832137

What Socratic 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 Socratic graph.