Evidence map›Paper›PMID 38820087›Full record

ArticleThe Journal of clinical endocrinology and metabolism2024

Single-Cell Analysis of Subcutaneous Fat Reveals Profibrotic Cells That Correlate With Visceral Adiposity in HIV.

Samuel S Bailin, Curtis L Gabriel, Rama D Gangula, LaToya Hannah, Sangeeta Nair, John Jeffrey Carr, James G Terry, Heidi J Silver, Joshua D Simmons, Mona Mashayekhi and 5 more

Abstract read
In one paragraph

Article in The Journal of clinical endocrinology and metabolism, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
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

10 citing papers in PubMed.

  1. Observational
  2. Review
  3. Review
  4. Unraveling Obesity: A Five-Year Integrative Review of Transcriptomic Data.International journal of molecular sciences · 2025
    Review
  5. Article
  6. Article
  7. Advances in Single-Cell Sequencing for Infectious Diseases: Progress and Perspectives.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  8. Lipodystrophy in HIV: Evolving Challenges and Unresolved Questions.International journal of molecular sciences · 2025
    Review
  9. Observational
  10. Article
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

15 authors.

Samuel S BailinDepartment of Medicine, Division of Infectious Diseases, Vanderbilt University Medical Center, Nashville, TN 37232, USA.ORCID 0000-0003-4990-1013
Curtis L GabrielDepartment of Medicine, Division of Gastroenterology, Hepatology, and Nutrition, Nashville, Vanderbilt University Medical Center, TN 37232, USA.
Rama D GangulaTennessee Center for AIDS Research, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
LaToya HannahDepartment of Medicine, Division of Diabetes, Endocrinology, and Metabolism, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Sangeeta NairDepartment of Radiology and Radiological Sciences, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
John Jeffrey CarrDepartment of Radiology and Radiological Sciences, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
James G TerryDepartment of Radiology and Radiological Sciences, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Heidi J SilverDepartment of Medicine, Division of Gastroenterology, Hepatology, and Nutrition, Nashville, Vanderbilt University Medical Center, TN 37232, USA.
Joshua D SimmonsTennessee Center for AIDS Research, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Mona MashayekhiDepartment of Medicine, Division of Diabetes, Endocrinology, and Metabolism, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Spyros A KalamsDepartment of Medicine, Division of Infectious Diseases, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Simon MallalDepartment of Medicine, Division of Infectious Diseases, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Jonathan A KropskiVeterans Affairs Tennessee Valley Healthcare System, Nashville, TN 37232, USA.
Celestine N WanjallaDepartment of Medicine, Division of Infectious Diseases, Vanderbilt University Medical Center, Nashville, TN 37232, USA.ORCID 0000-0001-9159-5414
John R KoetheDepartment of Medicine, Division of Infectious Diseases, Vanderbilt University Medical Center, Nashville, TN 37232, USA.

Funding

VANDERBILT UNIVERSITY CTSA FOR PEDIATRIC RESEARCHUL1RR024975 · NCRR · VANDERBILT UNIVERSITY · PI BERNARD, GORDON RAPHAEL · 2007 to 2011
$45.7M
Translational Analysis CoreP30DK058404 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI MARY Kay WASHINGTON · 2002 to 2026
$29.9M
Tennessee CFAR: Implementation of Culturally Responsive Trauma-Informed Care with Youth with HIV in Memphis, TNP30AI110527 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI John Koethe · 2015 to 2026
$27.5M
Institutional Career Development CoreKL2TR002245 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Julie A. Bastarache · 2017 to 2026
$9.3M
Spatiotemporal genomic regulation of disease initiation and progression in pulmonary fibrosisR01HL145372 · NHLBI · TRANSLATIONAL GENOMICS RESEARCH INST · PI Nicholas Eli Banovich, Jonathan Andrew Kropski · 2019 to 2026
$6.0M
Pathophysiology of Metabolically Detrimental Changes in Adipose Distribution, Adipocyte Function, and Adipose Immune Environment on Antiretroviral TherapyR01DK131529 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI SHEILA COLLINS, John Koethe · 2022 to 2026
$4.2M
The Role of Adipose-Resident T Cells in HIV-Associated Glucose IntoleranceR01DK112262 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI KOETHE, JOHN · 2017 to 2021
$3.8M
Vanderbilt SCHolars in HIV and Heart, Lung, Blood, and Sleep ReSearch (V-SCHoLARS, K12)K12HL143956 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI FREIBERG, MATTHEW S, KOETHE, JOHN · 2018 to 2022
$1.6M
Anti-cytomegalovirus Immune Responses in Atherosclerotic Cardiovascular Disease in Persons Living with HIVK23HL156759 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI WANJALLA, CELESTINE N · 2021 to 2025
$860k
Adipose Tissue T Cell Polarization and Metabolic Health in Persons Living with HIVK23DK135414 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Samuel Stuart Bailin · 2023 to 2026
$743k
The Effect of SGLT2 Inhibition on Adipose Tissue Inflammation and Endothelial FunctionK23HL159351 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Mona Mashayekhi · 2023 to 2026
$742k
Burroughs Wellcome Fund 1021480Doris Duke Charitable Foundation 2021193NCATS NIH HHS KL2 TR002245NCRR NIH HHS UL1 RR024975NCRR NIH HHS UL1RR024975NHLBI NIH HHS K12 HL143956NHLBI NIH HHS K23 HL156759NHLBI NIH HHS K23 HL159351NHLBI NIH HHS R01 HL145372NIAID NIH HHS P30 AI110527NIDDK NIH HHS K23 DK135414NIDDK NIH HHS P30 DK058404NIDDK NIH HHS R01 DK112262NIDDK NIH HHS R01 DK131529NIH HHS R01DK112262Tennessee Center for AIDS Research P30AI110527
6 · The paper itself

Abstract

contextCardiometabolic diseases are common in persons with HIV (PWH) on antiretroviral therapy (ART), which has been attributed to preferential lipid storage in visceral adipose tissue (VAT) compared with subcutaneous adipose tissue (SAT). However, the relationship of SAT-specific cellular and molecular programs with VAT volume is poorly understood in PWH.

objectiveWe characterized SAT cell-type specific composition and transcriptional programs that are associated with greater VAT volume in PWH on contemporary ART.

methodsWe enrolled PWH on long-term ART with a spectrum of metabolic health. Ninety-two participants underwent SAT biopsy for bulk RNA sequencing and 43 had single-cell RNA sequencing. Computed tomography quantified VAT volume and insulin resistance was calculated using the Homeostasis Model Assessment 2 Insulin Resistance (HOMA2-IR).

resultsVAT volume was associated with HOMA2-IR (P < .001). Higher proportions of SAT intermediate macrophages (IMs), myofibroblasts, and MYOC+ fibroblasts were associated with greater VAT volume using partial Spearman's correlation adjusting for age, sex, and body mass index (r = 0.34-0.49, P < .05 for all). Whole SAT transcriptomics showed PWH with greater VAT volume have increased expression of extracellular matrix (ECM)- and inflammation-associated genes, and reduced expression of lipolysis- and fatty acid metabolism-associated genes.

conclusionIn PWH, greater VAT volume is associated with a higher proportion of SAT IMs and fibroblasts, and a SAT ECM and inflammatory transcriptome, which is similar to findings in HIV-negative persons with obesity. These data identify SAT cell-type specific changes associated with VAT volume in PWH that could underlie the high rates of cardiometabolic diseases in PWH, though additional longitudinal studies are needed to define directionality and mechanisms.

Indexed as

HIV InfectionsIntra-Abdominal FatSingle-Cell AnalysisSubcutaneous FatAdiposityAdultFemaleFibrosisHumansInsulin ResistanceMaleMiddle AgedObesity, AbdominalHIVinflammationinsulin resistancesingle-cell RNA sequencingvisceral adipose tissue

Identifiers

PMID38820087
PMCPMC11651702

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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.