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Association of cystatin C levels with metabolic syndrome incidence: a nested case-control study with propensity score matching
OBJECTIVE: Metabolic syndrome (MetS) involves multiple metabolic disorders and seriously affects human health. Identification of key biological factors associated with MetS incidence is therefore important. We explored the association between MetS and the biochemical profiles of Chinese adults in Sh...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7812406/ https://www.ncbi.nlm.nih.gov/pubmed/33446006 http://dx.doi.org/10.1177/0300060520986311 |
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author | Yang, Tengfei Pei, Dongmei |
author_facet | Yang, Tengfei Pei, Dongmei |
author_sort | Yang, Tengfei |
collection | PubMed |
description | OBJECTIVE: Metabolic syndrome (MetS) involves multiple metabolic disorders and seriously affects human health. Identification of key biological factors associated with MetS incidence is therefore important. We explored the association between MetS and the biochemical profiles of Chinese adults in Shenyang City in a nested case-control study. METHODS: We included adult participants who underwent physical examination at our hospital for 2 consecutive years. Participants’ biochemical profiles and other MetS components were tested and monitored continuously. Propensity score matching was used to adjust confounding factors between participants with and without MetS. We analyzed the association between incidence of MetS and the biochemical profiles of participants. RESULTS: Of 5702 participants who underwent physical examination between 1 January 2017 and 1 December 2018, 538 had confirmed newly developed MetS. After successfully matching 436 pairs of participants, mean cystatin C (Cys-C) level was significantly higher in the MetS group than in the non-MetS group. Logistic regression analysis indicated that age (years) and γ-glutamate transpeptidase, creatinine, uric acid, and Cys-C levels were significantly associated with MetS incidence; among these, the odds ratio of Cys-C was highest (3.03; 95% confidence interval, 1.02–9.00). CONCLUSIONS: Cys-C levels were significantly associated with the incidence of MetS among Chinese adults. |
format | Online Article Text |
id | pubmed-7812406 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-78124062021-01-26 Association of cystatin C levels with metabolic syndrome incidence: a nested case-control study with propensity score matching Yang, Tengfei Pei, Dongmei J Int Med Res Retrospective Clinical Research Report OBJECTIVE: Metabolic syndrome (MetS) involves multiple metabolic disorders and seriously affects human health. Identification of key biological factors associated with MetS incidence is therefore important. We explored the association between MetS and the biochemical profiles of Chinese adults in Shenyang City in a nested case-control study. METHODS: We included adult participants who underwent physical examination at our hospital for 2 consecutive years. Participants’ biochemical profiles and other MetS components were tested and monitored continuously. Propensity score matching was used to adjust confounding factors between participants with and without MetS. We analyzed the association between incidence of MetS and the biochemical profiles of participants. RESULTS: Of 5702 participants who underwent physical examination between 1 January 2017 and 1 December 2018, 538 had confirmed newly developed MetS. After successfully matching 436 pairs of participants, mean cystatin C (Cys-C) level was significantly higher in the MetS group than in the non-MetS group. Logistic regression analysis indicated that age (years) and γ-glutamate transpeptidase, creatinine, uric acid, and Cys-C levels were significantly associated with MetS incidence; among these, the odds ratio of Cys-C was highest (3.03; 95% confidence interval, 1.02–9.00). CONCLUSIONS: Cys-C levels were significantly associated with the incidence of MetS among Chinese adults. SAGE Publications 2021-01-14 /pmc/articles/PMC7812406/ /pubmed/33446006 http://dx.doi.org/10.1177/0300060520986311 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Retrospective Clinical Research Report Yang, Tengfei Pei, Dongmei Association of cystatin C levels with metabolic syndrome incidence: a nested case-control study with propensity score matching |
title | Association of cystatin C levels with metabolic syndrome incidence: a nested case-control study with propensity score matching |
title_full | Association of cystatin C levels with metabolic syndrome incidence: a nested case-control study with propensity score matching |
title_fullStr | Association of cystatin C levels with metabolic syndrome incidence: a nested case-control study with propensity score matching |
title_full_unstemmed | Association of cystatin C levels with metabolic syndrome incidence: a nested case-control study with propensity score matching |
title_short | Association of cystatin C levels with metabolic syndrome incidence: a nested case-control study with propensity score matching |
title_sort | association of cystatin c levels with metabolic syndrome incidence: a nested case-control study with propensity score matching |
topic | Retrospective Clinical Research Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7812406/ https://www.ncbi.nlm.nih.gov/pubmed/33446006 http://dx.doi.org/10.1177/0300060520986311 |
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