Evidence map›Paper›PMID 37188226›Full record

ArticleDiabetes, metabolic syndrome and obesity : targets and therapy2023

Establishment of a Nomogram Based on Inflammatory Response-Related Methylation Sites in Intraoperative Visceral Adipose Tissue to Predict EWL% at One Year After LSG.

Guanyang Chen, Zhehong Li, Qing Sang, Liang Wang, Qiqige Wuyun, Zheng Wang, Weijian Chen, Chengyuan Yu, Dongbo Lian, Nengwei Zhang

Open access · goldAbstract read
In one paragraph

Article in Diabetes, metabolic syndrome and obesity : targets and therapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

2 citing papers in PubMed, 2 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 2 institutions in 1 country.

Guanyang Chen *Department of General Surgery, Peking University Ninth School of Clinical Medicine, Beijing, People's Republic of China.
Zhehong Li *Department of General Surgery, Beijing Shijitan Hospital, Capital Medical University, Beijing, People's Republic of China.ORCID 0000-0001-9385-0618
Qing Sang *Department of General Surgery, Peking University Ninth School of Clinical Medicine, Beijing, People's Republic of China.
Liang WangDepartment of General Surgery, Beijing Shijitan Hospital, Capital Medical University, Beijing, People's Republic of China.
Qiqige WuyunDepartment of General Surgery, Beijing Shijitan Hospital, Capital Medical University, Beijing, People's Republic of China.
Zheng WangDepartment of General Surgery, Beijing Shijitan Hospital, Capital Medical University, Beijing, People's Republic of China.
Weijian ChenDepartment of General Surgery, Beijing Shijitan Hospital, Capital Medical University, Beijing, People's Republic of China.
Chengyuan YuDepartment of General Surgery, Peking University Ninth School of Clinical Medicine, Beijing, People's Republic of China.
Dongbo LianDepartment of General Surgery, Beijing Shijitan Hospital, Capital Medical University, Beijing, People's Republic of China.
Nengwei ZhangDepartment of General Surgery, Beijing Shijitan Hospital, Capital Medical University, Beijing, People's Republic of China.ORCID 0000-0002-9412-2652
Capital Medical University · CNPeking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Laparoscopic sleeve gastrectomy (LSG) is considered as an effective bariatric and metabolic surgery for patients with severe obesity. Chronic low-grade inflammation of adipose tissue is associated with obesity and obesity-related complications. Objective: This study intends to establish a nomogram based on inflammatory response-related methylation sites in intraoperative visceral adipose tissue (VAT) to predict excess weight loss (EWL)% at one-year after LSG. Methods: Based on EWL% at one-year after LSG, patients were divided into two groups: the satisfied group (group-A, EWL%≥50%) and the unsatisfied group (group-B, EWL%<50%). Next, we defined genes corresponding to the methylation sites in the 850 K methylation microarray as methylation-related genes (MRGs). We then took the intersection of MRGs and inflammatory response-related genes. After that, inflammatory response-related methylation sites were identified based on overlapping genes. Moreover, difference analysis was carried out to obtain inflammatory response-related differentially methylated sites (IRRDMSs) between group-A and group-B. LASSO analysis was used to identify the hub methylation sites. Finally, we developed a nomogram based on the hub methylation sites. Results: There were 26 patients in the study, with 13 in group-A and 13 in group-B. After data filtering and difference analysis, 200 IRRDMSs were identified (143 hypermethylated sites and 57 hypomethylated sites). Then, we identified three hub methylation sites (cg03610073, cg03208951, and cg18746357) by LASSO analysis and built a predictive nomogram (Area under the curve=0.953). Conclusion: The predictive nomogram based on three inflammatory-related methylation sites (cg03610073, cg03208951, and cg18746357) in intraoperative visceral adipose tissue can predict one-year EWL% after LSG effectively.

Indexed as

DNA methylationexcess weight lossinflammationlaparoscopic sleeve gastrectomynomogram

Identifiers

PMID37188226
PMCPMC10178382
OpenAlexW4375864431

What Socratic holds

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LicenceCC BY-NC
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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.