Evidence map›Paper›PMID 32572626›Full record

ArticleSurgical endoscopy2021

Low visceral adipose tissue regulatory T cells are associated with higher comorbidity severity in patients undergoing bariatric surgery.

Anahita Jalilvand, Alecia Blaszczak, David Bradley, Joey Liu, Valerie Wright, Bradley Needleman, Willa Hsueh, Sabrena Noria

Abstract read
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In one paragraph

Article in Surgical endoscopy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
0.4field-weighted citation impact, top 35% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 6 citations in OpenAlex.

  1. Pooled it
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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

8 authors at 1 institution in 1 country.

Anahita JalilvandDepartment of Surgery, Ohio State University Wexner Medical Center, N718 Doan Hall, 410 W. 10th Ave., Columbus, OH, 43210, USA.ORCID http://orcid.org/0000-0002-4954-1938
Alecia BlaszczakDepartment of Surgery, Ohio State University Wexner Medical Center, N718 Doan Hall, 410 W. 10th Ave., Columbus, OH, 43210, USA.
David BradleyDepartment of Surgery, Ohio State University Wexner Medical Center, N718 Doan Hall, 410 W. 10th Ave., Columbus, OH, 43210, USA.
Joey LiuDepartment of Surgery, Ohio State University Wexner Medical Center, N718 Doan Hall, 410 W. 10th Ave., Columbus, OH, 43210, USA.
Valerie WrightDepartment of Surgery, Ohio State University Wexner Medical Center, N718 Doan Hall, 410 W. 10th Ave., Columbus, OH, 43210, USA.
Bradley NeedlemanDepartment of Surgery, Ohio State University Wexner Medical Center, N718 Doan Hall, 410 W. 10th Ave., Columbus, OH, 43210, USA.
Willa HsuehDepartment of Surgery, Ohio State University Wexner Medical Center, N718 Doan Hall, 410 W. 10th Ave., Columbus, OH, 43210, USA.
Sabrena NoriaDepartment of Surgery, Ohio State University Wexner Medical Center, N718 Doan Hall, 410 W. 10th Ave., Columbus, OH, 43210, USA. Sabrena.noria@osumc.edu.ORCID http://orcid.org/0000-0002-1260-6638
The Ohio State University Wexner Medical Center · US

Funding

Advanced Research Training in Immunology for Surgery Trainees (ARTIST)T32AI106704 · NIAID · OHIO STATE UNIVERSITY · PI GINNY L BUMGARDNER, Jon R Wisler · 2014 to 2026
$3.5M
NIAID NIH HHS T32 AI106704
6 · The paper itself

Abstract

backgroundAdipose tissue (AT) inflammation is linked to the development of type 2 diabetes (T2DM) and atherosclerosis in murine models of obesity. Reduced AT regulatory T cells (Tregs), which are anti-inflammatory immune cells, play an important part in this pathogenesis, and we have shown that AT-Tregs are inversely correlated to increasing body-mass-index. The purpose of this study was to evaluate the association between AT-Treg abundance and comorbidity status in patients undergoing bariatric surgery (BS).

methodsVisceral (intra-abdominal) AT was harvested at that time of primary BS (n = 80) and collagenase digested. AT-Treg abundance (CD4+/CD25+/FOXP3+) was characterized using flow cytometry from the AT stromal vascular fraction. The median AT-Treg abundance (3.03%) was utilized to define high (High-Tregs, n = 39) and low AT-Treg (low-Tregs, n = 38) abundance within this cohort. These two groups were compared in terms of baseline demographic data, preoperative obesity-related comorbidities, glycemic parameters, including insulin resistance (HOMA-IR).

resultsAge, excess body weight, and sex were not different between groups. Prevalence of hypertension, hyperlipidemia, or T2DM preoperatively were not different between groups. Compared to High-Tregs, patients with low-Tregs were more likely to have insulin-dependent type 2 diabetes (12.5% vs 2.9%, p = 0.04). Within patients with T2DM, low-Treg patients had higher plasma insulin levels compared to high-Tregs (31.8 (28.4-56.5) vs 15.5 (10.1-23.1), p = 0.04) and trended towards higher insulin resistance (HOMA-IR) (9.0 (5.3-18.3) vs 3.5 (2.2-7.7), p = 0.08). Within those diagnosed with hyperlipidemia, preoperative statin use was higher in Low-Treg patients compared to the control cohort (91% vs 50%, p = 0.056). Low-Treg patients with hypertension were more likely to need 2 + anti-hypertensive agents preoperatively compared to their counterparts (71% vs 44%, p = 0.058).

conclusionWithin bariatric candidates, lower visceral AT-Treg abundance was associated with increased baseline medication requirements for type 2 diabetes, hypertension, and hyperlipidemia. This suggests that reduced AT-Tregs may be associated with higher obesity-related comorbidity severity.

Indexed as

Bariatric SurgeryDiabetes Mellitus, Type 2AnimalsComorbidityHumansIntra-Abdominal FatMiceT-Lymphocytes, RegulatoryAdipose tissue inflammationBariatric surgeryObesityRegulatory T cells

Identifiers

PMID32572626
OpenAlexW3036256756

What OpenQuestion holds

Textmetadata
Read underepoch 390

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 OpenQuestion graph.