Cargando…
Relationship between multimorbidity, disease cluster and all-cause mortality among older adults: a retrospective cohort analysis
BACKGROUND: Previous studies have evaluated the association of multimorbidity with higher mortality, but epidemiologic data on the association between the disease clusters and all-cause mortality risk are rare. We aimed to examine the relationship between multimorbidity (number/ cluster) and all-cau...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8180153/ https://www.ncbi.nlm.nih.gov/pubmed/34090390 http://dx.doi.org/10.1186/s12889-021-11108-w |
_version_ | 1783703940751163392 |
---|---|
author | He, Kun Zhang, Wenli Hu, Xueqi Zhao, Hao Guo, Bingxin Shi, Zhan Zhao, Xiaoyan Yin, Chunyu Shi, Songhe |
author_facet | He, Kun Zhang, Wenli Hu, Xueqi Zhao, Hao Guo, Bingxin Shi, Zhan Zhao, Xiaoyan Yin, Chunyu Shi, Songhe |
author_sort | He, Kun |
collection | PubMed |
description | BACKGROUND: Previous studies have evaluated the association of multimorbidity with higher mortality, but epidemiologic data on the association between the disease clusters and all-cause mortality risk are rare. We aimed to examine the relationship between multimorbidity (number/ cluster) and all-cause mortality in Chinese older adults. METHODS: We conducted a population-based study of 50,100 Chinese participants. Multiple logistic regression analysis was used to estimate the impact of long-term conditions (LTCs) on all-cause mortality. RESULTS: The prevalence of multimorbidity was 31.35% and all-cause mortality was 8.01% (50,100 participants). In adjusted models, the odds ratios (ORs) and 95% confidence intervals (CIs) of all-cause mortality risk for those with 1, 2, and ≥ 3 LTCs compared with those with no LTCs was 1.45 (1.32–1.59), 1.72 (1.55–1.90), and 2.15 (1.85–2.50), respectively (P(trend) < 0.001). In the LTCs ≥2 category, the cluster of chronic diseases that included hypertension, diabetes, CHD, COPD, and stroke had the greatest impact on mortality. In the stratified model by age and sex, absolute all-cause mortality was higher among the ≥75 age group with an increasing number of LTCs. However, the relative effect size of the increasing number of LTCs on higher mortality risk was larger among those < 75 years. CONCLUSIONS: The risk of all-cause mortality is increased with the number of multimorbidity among Chinese older adults, particularly disease clusters. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12889-021-11108-w. |
format | Online Article Text |
id | pubmed-8180153 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-81801532021-06-07 Relationship between multimorbidity, disease cluster and all-cause mortality among older adults: a retrospective cohort analysis He, Kun Zhang, Wenli Hu, Xueqi Zhao, Hao Guo, Bingxin Shi, Zhan Zhao, Xiaoyan Yin, Chunyu Shi, Songhe BMC Public Health Research Article BACKGROUND: Previous studies have evaluated the association of multimorbidity with higher mortality, but epidemiologic data on the association between the disease clusters and all-cause mortality risk are rare. We aimed to examine the relationship between multimorbidity (number/ cluster) and all-cause mortality in Chinese older adults. METHODS: We conducted a population-based study of 50,100 Chinese participants. Multiple logistic regression analysis was used to estimate the impact of long-term conditions (LTCs) on all-cause mortality. RESULTS: The prevalence of multimorbidity was 31.35% and all-cause mortality was 8.01% (50,100 participants). In adjusted models, the odds ratios (ORs) and 95% confidence intervals (CIs) of all-cause mortality risk for those with 1, 2, and ≥ 3 LTCs compared with those with no LTCs was 1.45 (1.32–1.59), 1.72 (1.55–1.90), and 2.15 (1.85–2.50), respectively (P(trend) < 0.001). In the LTCs ≥2 category, the cluster of chronic diseases that included hypertension, diabetes, CHD, COPD, and stroke had the greatest impact on mortality. In the stratified model by age and sex, absolute all-cause mortality was higher among the ≥75 age group with an increasing number of LTCs. However, the relative effect size of the increasing number of LTCs on higher mortality risk was larger among those < 75 years. CONCLUSIONS: The risk of all-cause mortality is increased with the number of multimorbidity among Chinese older adults, particularly disease clusters. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12889-021-11108-w. BioMed Central 2021-06-05 /pmc/articles/PMC8180153/ /pubmed/34090390 http://dx.doi.org/10.1186/s12889-021-11108-w 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 Article He, Kun Zhang, Wenli Hu, Xueqi Zhao, Hao Guo, Bingxin Shi, Zhan Zhao, Xiaoyan Yin, Chunyu Shi, Songhe Relationship between multimorbidity, disease cluster and all-cause mortality among older adults: a retrospective cohort analysis |
title | Relationship between multimorbidity, disease cluster and all-cause mortality among older adults: a retrospective cohort analysis |
title_full | Relationship between multimorbidity, disease cluster and all-cause mortality among older adults: a retrospective cohort analysis |
title_fullStr | Relationship between multimorbidity, disease cluster and all-cause mortality among older adults: a retrospective cohort analysis |
title_full_unstemmed | Relationship between multimorbidity, disease cluster and all-cause mortality among older adults: a retrospective cohort analysis |
title_short | Relationship between multimorbidity, disease cluster and all-cause mortality among older adults: a retrospective cohort analysis |
title_sort | relationship between multimorbidity, disease cluster and all-cause mortality among older adults: a retrospective cohort analysis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8180153/ https://www.ncbi.nlm.nih.gov/pubmed/34090390 http://dx.doi.org/10.1186/s12889-021-11108-w |
work_keys_str_mv | AT hekun relationshipbetweenmultimorbiditydiseaseclusterandallcausemortalityamongolderadultsaretrospectivecohortanalysis AT zhangwenli relationshipbetweenmultimorbiditydiseaseclusterandallcausemortalityamongolderadultsaretrospectivecohortanalysis AT huxueqi relationshipbetweenmultimorbiditydiseaseclusterandallcausemortalityamongolderadultsaretrospectivecohortanalysis AT zhaohao relationshipbetweenmultimorbiditydiseaseclusterandallcausemortalityamongolderadultsaretrospectivecohortanalysis AT guobingxin relationshipbetweenmultimorbiditydiseaseclusterandallcausemortalityamongolderadultsaretrospectivecohortanalysis AT shizhan relationshipbetweenmultimorbiditydiseaseclusterandallcausemortalityamongolderadultsaretrospectivecohortanalysis AT zhaoxiaoyan relationshipbetweenmultimorbiditydiseaseclusterandallcausemortalityamongolderadultsaretrospectivecohortanalysis AT yinchunyu relationshipbetweenmultimorbiditydiseaseclusterandallcausemortalityamongolderadultsaretrospectivecohortanalysis AT shisonghe relationshipbetweenmultimorbiditydiseaseclusterandallcausemortalityamongolderadultsaretrospectivecohortanalysis |