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Sex-specific patterns and lifetime risk of multimorbidity in the general population: a 23-year prospective cohort study

BACKGROUND: Multimorbidity poses a major challenge for care coordination. However, data on what non-communicable diseases lead to multimorbidity, and whether the lifetime risk differs between men and women are lacking. We determined sex-specific differences in multimorbidity patterns and estimated s...

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Autores principales: Velek, Premysl, Luik, Annemarie I., Brusselle, Guy G. O., Stricker, Bruno Ch., Bindels, Patrick J. E., Kavousi, Maryam, Kieboom, Brenda C. T., Voortman, Trudy, Ruiter, Rikje, Ikram, M. Arfan, Ikram, M. Kamran, de Schepper, Evelien I. T., Licher, Silvan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9454172/
https://www.ncbi.nlm.nih.gov/pubmed/36071423
http://dx.doi.org/10.1186/s12916-022-02487-x
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author Velek, Premysl
Luik, Annemarie I.
Brusselle, Guy G. O.
Stricker, Bruno Ch.
Bindels, Patrick J. E.
Kavousi, Maryam
Kieboom, Brenda C. T.
Voortman, Trudy
Ruiter, Rikje
Ikram, M. Arfan
Ikram, M. Kamran
de Schepper, Evelien I. T.
Licher, Silvan
author_facet Velek, Premysl
Luik, Annemarie I.
Brusselle, Guy G. O.
Stricker, Bruno Ch.
Bindels, Patrick J. E.
Kavousi, Maryam
Kieboom, Brenda C. T.
Voortman, Trudy
Ruiter, Rikje
Ikram, M. Arfan
Ikram, M. Kamran
de Schepper, Evelien I. T.
Licher, Silvan
author_sort Velek, Premysl
collection PubMed
description BACKGROUND: Multimorbidity poses a major challenge for care coordination. However, data on what non-communicable diseases lead to multimorbidity, and whether the lifetime risk differs between men and women are lacking. We determined sex-specific differences in multimorbidity patterns and estimated sex-specific lifetime risk of multimorbidity in the general population. METHODS: We followed 6,094 participants from the Rotterdam Study aged 45 years and older for the occurrence of ten diseases (cancer, coronary heart disease, stroke, chronic obstructive pulmonary disease, depression, diabetes, dementia, asthma, heart failure, parkinsonism). We visualised participants’ trajectories from a single disease to multimorbidity and the most frequent combinations of diseases. We calculated sex-specific lifetime risk of multimorbidity, considering multimorbidity involving only somatic diseases (1) affecting the same organ system, (2) affecting different organ systems, and (3) multimorbidity involving depression. RESULTS: Over the follow-up period (1993–2016, median years of follow-up 9.2), we observed 6334 disease events. Of the study population, 10.3% had three or more diseases, and 27.9% had two or more diseases. The most frequent pair of co-occurring diseases among men was COPD and cancer (12.5% of participants with multimorbidity), the most frequent pair of diseases among women was depression and dementia (14.9%). The lifetime risk of multimorbidity was similar among men (66.0%, 95% CI: 63.2–68.8%) and women (65.1%, 95% CI: 62.5–67.7%), yet the risk of multimorbidity with depression was higher for women (30.9%, 95% CI: 28.4–33.5%, vs. 17.5%, 95% CI: 15.2–20.1%). The risk of multimorbidity with two diseases affecting the same organ is relatively low for both sexes (4.2% (95% CI: 3.2–5.5%) for men and 4.5% (95% CI: 3.5–5.7%) for women). CONCLUSIONS: Two thirds of people over 45 will develop multimorbidity in their remaining lifetime, with women at nearly double the risk of multimorbidity involving depression than men. These findings call for programmes of integrated care to consider sex-specific differences to ensure men and women are served equally. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12916-022-02487-x.
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spelling pubmed-94541722022-09-09 Sex-specific patterns and lifetime risk of multimorbidity in the general population: a 23-year prospective cohort study Velek, Premysl Luik, Annemarie I. Brusselle, Guy G. O. Stricker, Bruno Ch. Bindels, Patrick J. E. Kavousi, Maryam Kieboom, Brenda C. T. Voortman, Trudy Ruiter, Rikje Ikram, M. Arfan Ikram, M. Kamran de Schepper, Evelien I. T. Licher, Silvan BMC Med Research Article BACKGROUND: Multimorbidity poses a major challenge for care coordination. However, data on what non-communicable diseases lead to multimorbidity, and whether the lifetime risk differs between men and women are lacking. We determined sex-specific differences in multimorbidity patterns and estimated sex-specific lifetime risk of multimorbidity in the general population. METHODS: We followed 6,094 participants from the Rotterdam Study aged 45 years and older for the occurrence of ten diseases (cancer, coronary heart disease, stroke, chronic obstructive pulmonary disease, depression, diabetes, dementia, asthma, heart failure, parkinsonism). We visualised participants’ trajectories from a single disease to multimorbidity and the most frequent combinations of diseases. We calculated sex-specific lifetime risk of multimorbidity, considering multimorbidity involving only somatic diseases (1) affecting the same organ system, (2) affecting different organ systems, and (3) multimorbidity involving depression. RESULTS: Over the follow-up period (1993–2016, median years of follow-up 9.2), we observed 6334 disease events. Of the study population, 10.3% had three or more diseases, and 27.9% had two or more diseases. The most frequent pair of co-occurring diseases among men was COPD and cancer (12.5% of participants with multimorbidity), the most frequent pair of diseases among women was depression and dementia (14.9%). The lifetime risk of multimorbidity was similar among men (66.0%, 95% CI: 63.2–68.8%) and women (65.1%, 95% CI: 62.5–67.7%), yet the risk of multimorbidity with depression was higher for women (30.9%, 95% CI: 28.4–33.5%, vs. 17.5%, 95% CI: 15.2–20.1%). The risk of multimorbidity with two diseases affecting the same organ is relatively low for both sexes (4.2% (95% CI: 3.2–5.5%) for men and 4.5% (95% CI: 3.5–5.7%) for women). CONCLUSIONS: Two thirds of people over 45 will develop multimorbidity in their remaining lifetime, with women at nearly double the risk of multimorbidity involving depression than men. These findings call for programmes of integrated care to consider sex-specific differences to ensure men and women are served equally. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12916-022-02487-x. BioMed Central 2022-09-08 /pmc/articles/PMC9454172/ /pubmed/36071423 http://dx.doi.org/10.1186/s12916-022-02487-x Text en © The Author(s) 2022 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
Velek, Premysl
Luik, Annemarie I.
Brusselle, Guy G. O.
Stricker, Bruno Ch.
Bindels, Patrick J. E.
Kavousi, Maryam
Kieboom, Brenda C. T.
Voortman, Trudy
Ruiter, Rikje
Ikram, M. Arfan
Ikram, M. Kamran
de Schepper, Evelien I. T.
Licher, Silvan
Sex-specific patterns and lifetime risk of multimorbidity in the general population: a 23-year prospective cohort study
title Sex-specific patterns and lifetime risk of multimorbidity in the general population: a 23-year prospective cohort study
title_full Sex-specific patterns and lifetime risk of multimorbidity in the general population: a 23-year prospective cohort study
title_fullStr Sex-specific patterns and lifetime risk of multimorbidity in the general population: a 23-year prospective cohort study
title_full_unstemmed Sex-specific patterns and lifetime risk of multimorbidity in the general population: a 23-year prospective cohort study
title_short Sex-specific patterns and lifetime risk of multimorbidity in the general population: a 23-year prospective cohort study
title_sort sex-specific patterns and lifetime risk of multimorbidity in the general population: a 23-year prospective cohort study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9454172/
https://www.ncbi.nlm.nih.gov/pubmed/36071423
http://dx.doi.org/10.1186/s12916-022-02487-x
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