Evidence map›Paper›PMID 35641588›Full record

ArticleScientific reports2022

Adipose and serum zinc alpha-2-glycoprotein (ZAG) expressions predict longitudinal change of adiposity, wasting and predict survival in dialysis patients.

Gordon Chun-Kau Chan, Win Hlaing Than, Bonnie Ching-Ha Kwan, Ka-Bik Lai, Ronald Cheong-Kin Chan, Jeremy Yuen-Chun Teoh, Jack Kit-Chung Ng, Kai-Ming Chow, Winston Wing-Shing Fung, Phyllis Mei-Shan Cheng and 4 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 16% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
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  3. ZnScientific reports · 2025
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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

14 authors at 2 institutions in 1 country.

Gordon Chun-Kau ChanDepartment of Medicine and Therapeutics, Prince of Wales Hospital, Carol & Richard Yu Peritoneal Dialysis Research Centre, The Chinese University of Hong Kong, Shatin, NT, Hong Kong, China. cck295@ha.org.hk.
Win Hlaing ThanDepartment of Medicine and Therapeutics, Prince of Wales Hospital, Carol & Richard Yu Peritoneal Dialysis Research Centre, The Chinese University of Hong Kong, Shatin, NT, Hong Kong, China.
Bonnie Ching-Ha KwanDepartment of Medicine and Therapeutics, Prince of Wales Hospital, Carol & Richard Yu Peritoneal Dialysis Research Centre, The Chinese University of Hong Kong, Shatin, NT, Hong Kong, China.
Ka-Bik LaiDepartment of Medicine and Therapeutics, Prince of Wales Hospital, Carol & Richard Yu Peritoneal Dialysis Research Centre, The Chinese University of Hong Kong, Shatin, NT, Hong Kong, China.
Ronald Cheong-Kin ChanDepartment of Anatomical and Cellular Pathology, The Chinese University of Hong Kong, Shatin, Hong Kong, China.
Jeremy Yuen-Chun TeohDepartment of Surgery, S.H. Ho Urology Centre, The Chinese University of Hong Kong, Shatin, Hong Kong, China.
Jack Kit-Chung NgDepartment of Medicine and Therapeutics, Prince of Wales Hospital, Carol & Richard Yu Peritoneal Dialysis Research Centre, The Chinese University of Hong Kong, Shatin, NT, Hong Kong, China.
Kai-Ming ChowDepartment of Medicine and Therapeutics, Prince of Wales Hospital, Carol & Richard Yu Peritoneal Dialysis Research Centre, The Chinese University of Hong Kong, Shatin, NT, Hong Kong, China.
Winston Wing-Shing FungDepartment of Medicine and Therapeutics, Prince of Wales Hospital, Carol & Richard Yu Peritoneal Dialysis Research Centre, The Chinese University of Hong Kong, Shatin, NT, Hong Kong, China.
Phyllis Mei-Shan ChengDepartment of Medicine and Therapeutics, Prince of Wales Hospital, Carol & Richard Yu Peritoneal Dialysis Research Centre, The Chinese University of Hong Kong, Shatin, NT, Hong Kong, China.
Man-Ching LawDepartment of Medicine and Therapeutics, Prince of Wales Hospital, Carol & Richard Yu Peritoneal Dialysis Research Centre, The Chinese University of Hong Kong, Shatin, NT, Hong Kong, China.
Chi-Bon LeungDepartment of Medicine and Therapeutics, Prince of Wales Hospital, Carol & Richard Yu Peritoneal Dialysis Research Centre, The Chinese University of Hong Kong, Shatin, NT, Hong Kong, China.
Philip Kam-Tao LiDepartment of Medicine and Therapeutics, Prince of Wales Hospital, Carol & Richard Yu Peritoneal Dialysis Research Centre, The Chinese University of Hong Kong, Shatin, NT, Hong Kong, China.
Cheuk-Chun SzetoDepartment of Medicine and Therapeutics, Prince of Wales Hospital, Carol & Richard Yu Peritoneal Dialysis Research Centre, The Chinese University of Hong Kong, Shatin, NT, Hong Kong, China.
Prince of Wales Hospital · CNChinese University of Hong Kong · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There were limited data on adipose and serum zinc alpha-2-glycoprotein (ZAG) expression and its association with body composition in patients with advanced chronic kidney disease (CKD). This study aimed to quantify adipose and serum ZAG expression and evaluate their association with body composition and its longitudinal change, together with mortality in incident dialysis patients. We performed a single-center prospective cohort study. Patients who were planned for peritoneal dialysis were recruited. ZAG levels were measured from serum sample, subcutaneous and pre-peritoneal fat tissue obtained during peritoneal dialysis catheter insertion. Body composition and functional state were evaluated by bioimpedance spectroscopy and Clinical Frailty Scale respectively at baseline and were repeated 1 year later. Primary outcome was 2-year survival. Secondary outcomes were longitudinal changes of body composition. At baseline, the average adipose and serum ZAG expression was 13.4 ± 130.0-fold and 74.7 ± 20.9 µg/ml respectively. Both adipose and serum ZAG expressions independently predicted adipose tissue mass (ATM) (p = 0.001, p = 0.008, respectively). At 1 year, ATM increased by 3.3 ± 7.4 kg (p < 0.001) while lean tissue mass (LTM) remained similar (p = 0.5). Adipose but not serum ZAG level predicted change in ATM (p = 0.007) and LTM (p = 0.01). Serum ZAG level predicted overall survival (p = 0.005) and risk of infection-related death (p = 0.045) after adjusting for confounders. In conclusion, adipose and serum ZAG levels negatively correlated with adiposity and predicted its longitudinal change of fat and lean tissue mass, whilst serum ZAG predicted survival independent of body mass in advanced CKD patient.

Indexed as

AdiposityCachexiaRenal DialysisRenal Insufficiency, ChronicZn-Alpha-2-GlycoproteinAdipokinesAdipose TissueHumansObesityProspective StudiesSeminal Plasma ProteinsSurvival RateAdipokinesAZGP1 protein, humanSeminal Plasma ProteinsZn-Alpha-2-Glycoprotein

Identifiers

PMID35641588
PMCPMC9158927
OpenAlexW4281934008

What OpenQuestion holds

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LicenceCC BY
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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.