Evidence mapPaperPMID 37745703Full record

ArticleFrontiers in endocrinology2023

Association of alpha-aminoadipic acid with cardiometabolic risk factors in healthy and high-risk individuals.

Stacy Desine, Curtis L Gabriel, Holly M Smith, Olivia R Antonetti, Chuan Wang, M Wade Calcutt, Amanda C Doran, Heidi J Silver, Sangeeta Nair, James G Terry and 5 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in endocrinology, 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
5.6field-weighted citation impact, top 4% 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, 16 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 2 institutions in 1 country.

Stacy DesineDivision of Cardiovascular Medicine, Vanderbilt University Medical Center, Nashville, TN, United States.
Curtis L GabrielDivision of Gastroenterology, Hepatology and Nutrition, Vanderbilt University Medical Center, Nashville, TN, United States.
Holly M SmithDivision of Cardiovascular Medicine, Vanderbilt University Medical Center, Nashville, TN, United States.
Olivia R AntonettiDivision of Cardiovascular Medicine, Vanderbilt University Medical Center, Nashville, TN, United States.
Chuan WangDivision of Cardiovascular Medicine, Vanderbilt University Medical Center, Nashville, TN, United States.
M Wade CalcuttDepartment of Biochemistry, Mass Spectrometry Research Center, Vanderbilt University, Nashville, TN, United States.
Amanda C DoranDivision of Cardiovascular Medicine, Vanderbilt University Medical Center, Nashville, TN, United States.
Heidi J SilverDivision of Gastroenterology, Hepatology and Nutrition, Vanderbilt University Medical Center, Nashville, TN, United States.
Sangeeta NairDepartment of Radiology and Radiological Sciences, Vanderbilt University Medical Center, Nashville, TN, United States.
James G TerryDepartment of Radiology and Radiological Sciences, Vanderbilt University Medical Center, Nashville, TN, United States.
John Jeffrey CarrDepartment of Radiology and Radiological Sciences, Vanderbilt University Medical Center, Nashville, TN, United States.
MacRae F LintonDivision of Cardiovascular Medicine, Vanderbilt University Medical Center, Nashville, TN, United States.
Jonathan D BrownDivision of Cardiovascular Medicine, Vanderbilt University Medical Center, Nashville, TN, United States.
John R KoetheDivision of Infectious Diseases, Vanderbilt University Medical Center, Nashville, TN, United States.
Jane F FergusonDivision of Cardiovascular Medicine, Vanderbilt University Medical Center, Nashville, TN, United States.
Vanderbilt University Medical Center · USVanderbilt University · US

Funding

Non-Coding RNA Analytical CoreP01HL116263 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · 2022 to 2025
$17.7M
Vanderbilt Institute for Clinical and Translational Research (VICTR)UL1TR002243 · VANDERBILT UNIVERSITY MEDICAL CENTER · 2025 to 2025
$10.7M
Translational Analysis CoreP30DK058404 · VANDERBILT UNIVERSITY MEDICAL CENTER · 2002 to 2025
$4.9M
Tennessee Center for AIDS Research (TN-CFAR)P30AI110527 · VANDERBILT UNIVERSITY MEDICAL CENTER · 2025 to 2025
$1.7M
Critical Mediators of Inflammation Resolution and Immune Memory in AtherosclerosisR01HL159487 · VANDERBILT UNIVERSITY MEDICAL CENTER · 2025 to 2025
$581k
NCATS NIH HHS UL1 TR002243NHLBI NIH HHS K12 HL143956NHLBI NIH HHS P01 HL116263NHLBI NIH HHS R01 HL159487NIAID NIH HHS P30 AI110527NIDDK NIH HHS P30 DK058404NIDDK NIH HHS R01 DK112262NIDDK NIH HHS R01 DK117144
6 · The paper itself

Abstract

Introduction: Plasma levels of the metabolite alpha-aminoadipic acid (2-AAA) have been associated with risk of type 2 diabetes (T2D) and atherosclerosis. However, little is known about the relationship of 2-AAA to other cardiometabolic risk markers in pre-disease states, or in the setting of comorbid disease. Methods: We measured circulating 2-AAA using two methods in 1) a sample of 261 healthy individuals (2-AAA Study), and 2) in a sample of 134 persons comprising 110 individuals with treated HIV, with or without T2D, a population at high risk of metabolic disease and cardiovascular events despite suppression of circulating virus, and 24 individuals with T2D without HIV (HATIM Study). We examined associations between plasma 2-AAA and markers of cardiometabolic health within each cohort. Results and discussion: We observed differences in 2-AAA by sex and race in both cohorts, with higher levels observed in men compared with women, and in Asian compared with Black or white individuals (P<0.05). There was no significant difference in 2-AAA by HIV status within individuals with T2D in the HATIM Study. We confirmed associations between 2-AAA and dyslipidemia in both cohorts, where high 2-AAA associated with low HDL cholesterol (P<0.001) and high triglycerides (P<0.05). As expected, within the cohort of people with HIV, 2-AAA was higher in the setting of T2D compared to pre-diabetes or normoglycemia (P<0.001). 2-AAA was positively associated with body mass index (BMI) in the 2-AAA Study, and with waist circumference and measures of visceral fat volume in HATIM (all P<0.05). Further, 2-AAA associated with increased liver fat in persons with HIV (P<0.001). Our study confirms 2-AAA as a marker of cardiometabolic risk in both healthy individuals and those at high cardiometabolic risk, reveals relationships with adiposity and hepatic steatosis, and highlights important differences by sex and race. Further studies are warranted to establish molecular mechanisms linking 2-AAA to disease in other high-risk populations.

Indexed as

Cardiovascular DiseasesDiabetes Mellitus, Type 2HIV Infections2-Aminoadipic AcidCardiometabolic Risk FactorsFemaleHumansMale2-Aminoadipic Acid2-AAAbiomarkercardiometabolic diseasediabetesHIV

Identifiers

PMID37745703
PMCPMC10513411
OpenAlexW4386523438

What Socratic holds

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LicenceCC BY
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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 Socratic graph.