Evidence map›Paper›PMID 36406322›Full record

ArticleJournal of clinical and translational hepatology2023

Dissecting the Contributing Role of Divergent Adipose Tissue to Multidimensional Frailty in Cirrhosis.

Lihong Mao, Chaoqun Li, Xiaoyu Wang, Mingyu Sun, Yifan Li, Zihan Yu, Binxin Cui, Gaoyue Guo, Wanting Yang, Yangyang Hui and 4 more

Open access · diamondAbstract read
In one paragraph

Article in Journal of clinical and translational hepatology, 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
0.5field-weighted citation impact, top 39% 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, 5 citations in OpenAlex.

  1. Article
  2. 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

14 authors at 1 institution in 1 country.

Lihong MaoDepartment of Gastroenterology and Hepatology, Tianjin Medical University General Hospital, Tianjin, China.
Chaoqun LiDepartment of Gastroenterology and Hepatology, Tianjin Medical University General Hospital, Tianjin, China.
Xiaoyu WangDepartment of Gastroenterology and Hepatology, Tianjin Medical University General Hospital, Tianjin, China.
Mingyu SunDepartment of Gastroenterology and Hepatology, Tianjin Medical University General Hospital, Tianjin, China.
Yifan LiDepartment of Gastroenterology and Hepatology, Tianjin Medical University General Hospital, Tianjin, China.
Zihan YuDepartment of Gastroenterology and Hepatology, Tianjin Medical University General Hospital, Tianjin, China.
Binxin CuiDepartment of Gastroenterology, Tianjin Medical University General Hospital Airport Hospital, Tianjin, China.
Gaoyue GuoDepartment of Gastroenterology and Hepatology, Tianjin Medical University General Hospital, Tianjin, China.
Wanting YangDepartment of Gastroenterology and Hepatology, Tianjin Medical University General Hospital, Tianjin, China.
Yangyang HuiDepartment of Gastroenterology and Hepatology, Tianjin Medical University General Hospital, Tianjin, China.
Xiaofei FanDepartment of Gastroenterology and Hepatology, Tianjin Medical University General Hospital, Tianjin, China.
Jie ZhangDepartment of Gastroenterology and Hepatology, Tianjin Medical University General Hospital, Tianjin, China.
Kui JiangDepartment of Gastroenterology and Hepatology, Tianjin Medical University General Hospital, Tianjin, China.
Chao SunDepartment of Gastroenterology and Hepatology, Tianjin Medical University General Hospital, Tianjin, China.ORCID https://orcid.org/0000-0002-0380-7999
Tianjin Medical University General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Aims: Emerging evidence has demonstrated that abnormal body composition may potentiate the development of frailty, whereas little work focuses on the role of divergent adipose tissue. Therefore, we aimed to determine the potential contribution of adipose tissue distribution to multidimensional frailty in decompensated cirrhosis. Methods: We conducted a retrospective cohort study. Divergent adipose tissues were assessed by computed tomography-derived subcutaneous adipose tissue index (SATI), visceral adipose tissue index (VATI) and total adipose tissue index (TATI), respectively. Frailty was identified by our validated self-reported Frailty Index. Multiple binary logistic models incorporating different covariates were established to assess the relationship between adipose tissue distribution and frailty. Results: The study cohort comprised 245 cirrhotic patients with 45.3% being male. The median Frailty Index, body mass index (BMI) and model for end-stage liver disease (MELD) score were 0.11, 24.3 kg/m Conclusions: In the context of decompensated cirrhosis, low SATI and concomitant TATI were associated with higher risk of being frail. These findings highlight the importance to further apply tissue-specific tools of body composition in place of crude metric like BMI.

Indexed as

Adipose tissueFrailtyLiver cirrhosisSubcutaneous adipose tissue index

Identifiers

PMID36406322
PMCPMC9647104
OpenAlexW4224299003

What OpenQuestion holds

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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 OpenQuestion graph.