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Association of lipid accumulation product with chronic kidney disease in Chinese community adults: a report from the REACTION study
BACKGROUND: Limited studies regarding the correlation of lipid accumulation product (LAP) with a decreased estimated glomerular filtration rate (eGFR) have yielded conflicting findings, and no report has demonstrated the relationship of LAP with chronic kidney disease (CKD), defined as the presence...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8502407/ https://www.ncbi.nlm.nih.gov/pubmed/34627270 http://dx.doi.org/10.1186/s12944-021-01569-8 |
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author | Yan, Pijun Xu, Yong Miao, Ying Tang, Qian Wu, Yuru Bai, Xue Zhang, Zhihong Li, Qian Wan, Qin |
author_facet | Yan, Pijun Xu, Yong Miao, Ying Tang, Qian Wu, Yuru Bai, Xue Zhang, Zhihong Li, Qian Wan, Qin |
author_sort | Yan, Pijun |
collection | PubMed |
description | BACKGROUND: Limited studies regarding the correlation of lipid accumulation product (LAP) with a decreased estimated glomerular filtration rate (eGFR) have yielded conflicting findings, and no report has demonstrated the relationship of LAP with chronic kidney disease (CKD), defined as the presence of albuminuria and/or a decreased eGFR. The purpose of this study was to estimate the possible correlation of LAP with CKD prevalence in Chinese community adults. METHOD: In this cross-sectional study, LAP level of 7202 participants (age ≥ 40 years) was determined, and its possible association with CKD was evaluated by a multiple logistic regression model. RESULTS: Compared with subjects with non-CKD, non-albuminuria, and high eGFR, LAP levels significantly increased in female not male subjects with CKD, albuminuria, and low eGFR, respectively (all P < 0.001). The univariate logistic regression analysis revealed that LAP level of female not male subjects were significantly and positively associated with the prevalence of CKD (P < 0.001). The multivariate logistic regression analysis showed that the risk of CKD prevalence in female not male subjects progressively increased across LAP quartiles (P for trend < 0.01), and the risk of CKD prevalence of subjects in Q4 significantly increased compared to those in Q1 after adjustment for potential confounding factors in Models 4 (odds ratio [OR]: 1.382, 95% confidence intervals [CI] 1.002–1.906, P < 0.05). Stratified analysis revealed positive associations of LAP quartiles with risk of CKD prevalence in people with the following characteristics: women, older, overweight, with hypertension, normal glucose tolerance, appropriate low-density lipoprotein cholesterol, nonsmokers, nondrinkers, and no cardiovascular disease events. CONCLUSIONS: High LAP levels might be significantly associated with risk of CKD prevalence in community-dwelling Chinese female adults, which may inform both public health recommendations and clinical practice. |
format | Online Article Text |
id | pubmed-8502407 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-85024072021-10-20 Association of lipid accumulation product with chronic kidney disease in Chinese community adults: a report from the REACTION study Yan, Pijun Xu, Yong Miao, Ying Tang, Qian Wu, Yuru Bai, Xue Zhang, Zhihong Li, Qian Wan, Qin Lipids Health Dis Research BACKGROUND: Limited studies regarding the correlation of lipid accumulation product (LAP) with a decreased estimated glomerular filtration rate (eGFR) have yielded conflicting findings, and no report has demonstrated the relationship of LAP with chronic kidney disease (CKD), defined as the presence of albuminuria and/or a decreased eGFR. The purpose of this study was to estimate the possible correlation of LAP with CKD prevalence in Chinese community adults. METHOD: In this cross-sectional study, LAP level of 7202 participants (age ≥ 40 years) was determined, and its possible association with CKD was evaluated by a multiple logistic regression model. RESULTS: Compared with subjects with non-CKD, non-albuminuria, and high eGFR, LAP levels significantly increased in female not male subjects with CKD, albuminuria, and low eGFR, respectively (all P < 0.001). The univariate logistic regression analysis revealed that LAP level of female not male subjects were significantly and positively associated with the prevalence of CKD (P < 0.001). The multivariate logistic regression analysis showed that the risk of CKD prevalence in female not male subjects progressively increased across LAP quartiles (P for trend < 0.01), and the risk of CKD prevalence of subjects in Q4 significantly increased compared to those in Q1 after adjustment for potential confounding factors in Models 4 (odds ratio [OR]: 1.382, 95% confidence intervals [CI] 1.002–1.906, P < 0.05). Stratified analysis revealed positive associations of LAP quartiles with risk of CKD prevalence in people with the following characteristics: women, older, overweight, with hypertension, normal glucose tolerance, appropriate low-density lipoprotein cholesterol, nonsmokers, nondrinkers, and no cardiovascular disease events. CONCLUSIONS: High LAP levels might be significantly associated with risk of CKD prevalence in community-dwelling Chinese female adults, which may inform both public health recommendations and clinical practice. BioMed Central 2021-10-09 /pmc/articles/PMC8502407/ /pubmed/34627270 http://dx.doi.org/10.1186/s12944-021-01569-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Yan, Pijun Xu, Yong Miao, Ying Tang, Qian Wu, Yuru Bai, Xue Zhang, Zhihong Li, Qian Wan, Qin Association of lipid accumulation product with chronic kidney disease in Chinese community adults: a report from the REACTION study |
title | Association of lipid accumulation product with chronic kidney disease in Chinese community adults: a report from the REACTION study |
title_full | Association of lipid accumulation product with chronic kidney disease in Chinese community adults: a report from the REACTION study |
title_fullStr | Association of lipid accumulation product with chronic kidney disease in Chinese community adults: a report from the REACTION study |
title_full_unstemmed | Association of lipid accumulation product with chronic kidney disease in Chinese community adults: a report from the REACTION study |
title_short | Association of lipid accumulation product with chronic kidney disease in Chinese community adults: a report from the REACTION study |
title_sort | association of lipid accumulation product with chronic kidney disease in chinese community adults: a report from the reaction study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8502407/ https://www.ncbi.nlm.nih.gov/pubmed/34627270 http://dx.doi.org/10.1186/s12944-021-01569-8 |
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