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Gender specific somatic symptom burden and mortality risk in the general population
Gender specific all-cause mortality risk associated with a high somatic symptom burden (SSB) in a population-based cohort was investigated. The study population included 5679 women and 5861 men aged 25–74 years from the population-based MONICA/KORA Cohort. SSB was assessed following the Somatic Symp...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9445038/ https://www.ncbi.nlm.nih.gov/pubmed/36065007 http://dx.doi.org/10.1038/s41598-022-18814-4 |
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author | Atasoy, Seryan Hausteiner-Wiehle, Constanze Sattel, Heribert Johar, Hamimatunnisa Roenneberg, Casper Peters, Annette Ladwig, Karl-Heinz Henningsen, Peter |
author_facet | Atasoy, Seryan Hausteiner-Wiehle, Constanze Sattel, Heribert Johar, Hamimatunnisa Roenneberg, Casper Peters, Annette Ladwig, Karl-Heinz Henningsen, Peter |
author_sort | Atasoy, Seryan |
collection | PubMed |
description | Gender specific all-cause mortality risk associated with a high somatic symptom burden (SSB) in a population-based cohort was investigated. The study population included 5679 women and 5861 men aged 25–74 years from the population-based MONICA/KORA Cohort. SSB was assessed following the Somatic Symptom Scale-8 and categorized as very high (≥ 95th percentile), high (60–95th percentile), moderate (30–60th percentile), and low (≤ 30th percentile). The impact of SSB on all-cause mortality risk within a mean follow-up period of 22.6 years (SD 7.1; 267,278 person years) was estimated by gender-specific Cox regression models adjusted for sociodemographic, lifestyle, somatic and psychosocial risk factors, as well as pre-existing medical conditions. Approximately 5.7% of men and 7.3% of women had very high SSB. During follow-up, 3638 (30.6%) mortality cases were observed. Men with a very-high SSB had 48% increased relative risk of mortality in comparison to men with a low SSB after adjustment for concurrent risk factors (1.48, 95% CI 1.20–1.81, p < .0001), corresponding to 2% increased risk of mortality for each 1-point increment in SSB (1.02; 95% CI 1.01–1.03; p = 0.03). In contrast, women with a very high SSB had a 22% lower risk of mortality (0.78, 95% CI 0.61–1.00, p = 0.05) and women with high SSB had an 18% lower risk of mortality (0.82; 95% CI 0.68–0.98, p = 0.03) following adjustment for concurrent risk factors. The current findings indicate that an increasing SSB is an independent risk factor for mortality in men but not in women, pointing in the direction of critical gender differences in the management of SSB, including women’s earlier health care utilization than men. |
format | Online Article Text |
id | pubmed-9445038 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-94450382022-09-07 Gender specific somatic symptom burden and mortality risk in the general population Atasoy, Seryan Hausteiner-Wiehle, Constanze Sattel, Heribert Johar, Hamimatunnisa Roenneberg, Casper Peters, Annette Ladwig, Karl-Heinz Henningsen, Peter Sci Rep Article Gender specific all-cause mortality risk associated with a high somatic symptom burden (SSB) in a population-based cohort was investigated. The study population included 5679 women and 5861 men aged 25–74 years from the population-based MONICA/KORA Cohort. SSB was assessed following the Somatic Symptom Scale-8 and categorized as very high (≥ 95th percentile), high (60–95th percentile), moderate (30–60th percentile), and low (≤ 30th percentile). The impact of SSB on all-cause mortality risk within a mean follow-up period of 22.6 years (SD 7.1; 267,278 person years) was estimated by gender-specific Cox regression models adjusted for sociodemographic, lifestyle, somatic and psychosocial risk factors, as well as pre-existing medical conditions. Approximately 5.7% of men and 7.3% of women had very high SSB. During follow-up, 3638 (30.6%) mortality cases were observed. Men with a very-high SSB had 48% increased relative risk of mortality in comparison to men with a low SSB after adjustment for concurrent risk factors (1.48, 95% CI 1.20–1.81, p < .0001), corresponding to 2% increased risk of mortality for each 1-point increment in SSB (1.02; 95% CI 1.01–1.03; p = 0.03). In contrast, women with a very high SSB had a 22% lower risk of mortality (0.78, 95% CI 0.61–1.00, p = 0.05) and women with high SSB had an 18% lower risk of mortality (0.82; 95% CI 0.68–0.98, p = 0.03) following adjustment for concurrent risk factors. The current findings indicate that an increasing SSB is an independent risk factor for mortality in men but not in women, pointing in the direction of critical gender differences in the management of SSB, including women’s earlier health care utilization than men. Nature Publishing Group UK 2022-09-05 /pmc/articles/PMC9445038/ /pubmed/36065007 http://dx.doi.org/10.1038/s41598-022-18814-4 Text en © The Author(s) 2022, corrected publication 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) . |
spellingShingle | Article Atasoy, Seryan Hausteiner-Wiehle, Constanze Sattel, Heribert Johar, Hamimatunnisa Roenneberg, Casper Peters, Annette Ladwig, Karl-Heinz Henningsen, Peter Gender specific somatic symptom burden and mortality risk in the general population |
title | Gender specific somatic symptom burden and mortality risk in the general population |
title_full | Gender specific somatic symptom burden and mortality risk in the general population |
title_fullStr | Gender specific somatic symptom burden and mortality risk in the general population |
title_full_unstemmed | Gender specific somatic symptom burden and mortality risk in the general population |
title_short | Gender specific somatic symptom burden and mortality risk in the general population |
title_sort | gender specific somatic symptom burden and mortality risk in the general population |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9445038/ https://www.ncbi.nlm.nih.gov/pubmed/36065007 http://dx.doi.org/10.1038/s41598-022-18814-4 |
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