Age‐Specific Associations of Usual Blood Pressure Variability With Cardiovascular Disease and Mortality: 10‐Year Diabetes Mellitus Cohort Study

Background The detrimental effects of increased variability in systolic blood pressure (SBP) on cardiovascular disease (CVD) and mortality risk in patients with diabetes mellitus remains unclear. This study evaluated age‐specific association of usual SBP visit‐to‐visit variability with CVD and morta...

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التفاصيل البيبلوغرافية
الحاوية / القاعدة:Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
المؤلفون الرئيسيون: Eric Yuk Fai Wan, Esther Yee Tak Yu, Weng Yee Chin, Jessica K. Barrett, Ian Chi Kei Wong, Esther Wai Yin Chan, Celine Sze Ling Chui, Shiqi Chen, Cindy Lo Kuen Lam
التنسيق: مقال
اللغة:الإنجليزية
منشور في: Wiley 2021-09-01
الموضوعات:
الوصول للمادة أونلاين:https://www.ahajournals.org/doi/10.1161/JAHA.120.019026
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author Eric Yuk Fai Wan
Esther Yee Tak Yu
Weng Yee Chin
Jessica K. Barrett
Ian Chi Kei Wong
Esther Wai Yin Chan
Celine Sze Ling Chui
Shiqi Chen
Cindy Lo Kuen Lam
author_facet Eric Yuk Fai Wan
Esther Yee Tak Yu
Weng Yee Chin
Jessica K. Barrett
Ian Chi Kei Wong
Esther Wai Yin Chan
Celine Sze Ling Chui
Shiqi Chen
Cindy Lo Kuen Lam
author_sort Eric Yuk Fai Wan
collection DOAJ
container_title Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
description Background The detrimental effects of increased variability in systolic blood pressure (SBP) on cardiovascular disease (CVD) and mortality risk in patients with diabetes mellitus remains unclear. This study evaluated age‐specific association of usual SBP visit‐to‐visit variability with CVD and mortality in patients with type 2 diabetes mellitus. Methods and Results A retrospective cohort study investigated 155 982 patients with diabetes mellitus aged 45 to 84 years without CVD at baseline (2008–2010). Usual SBP variability was estimated using SBP SD obtained from a mixed‐effects model. Age‐specific associations (45–54, 55–64, 65–74, 75–84 years) between usual SBP variability, CVD, and mortality risk were assessed by Cox regression adjusted for patient characteristics. After a median follow‐up of 9.7 years, 49 816 events (including 34 039 CVD events and 29 211 mortalities) were identified. Elevated SBP variability was independently, positively, and log‐linearly associated with higher CVD and mortality risk among all age groups, with no evidence of any threshold effects. The excess CVD and mortality risk per 5 mm Hg increase in SBP variability within the 45 to 54 age group is >3 times higher than the 70 to 79 age group (hazard ratio, 1.66; 95% CI, 1.49–1.85 versus hazard ratio, 1.19; 95% CI, 1.15–1.23). The significant associations remained consistent among all subgroups. Patients with younger age had a higher association of SBP variability with event outcomes. Conclusions The findings suggest that SBP visit‐to‐visit variability was strongly associated with CVD and mortality with no evidence of a threshold effect in a population with diabetes mellitus. As well as controlling overall blood pressure levels, SBP visit‐to‐visit variability should be monitored and evaluated in routine practice, in particular for younger patients.
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spelling doaj-art-e609953b0cc34abd8a9b7053b256a19a2025-08-19T21:16:12ZengWileyJournal of the American Heart Association: Cardiovascular and Cerebrovascular Disease2047-99802021-09-01101710.1161/JAHA.120.019026Age‐Specific Associations of Usual Blood Pressure Variability With Cardiovascular Disease and Mortality: 10‐Year Diabetes Mellitus Cohort StudyEric Yuk Fai Wan0Esther Yee Tak Yu1Weng Yee Chin2Jessica K. Barrett3Ian Chi Kei Wong4Esther Wai Yin Chan5Celine Sze Ling Chui6Shiqi Chen7Cindy Lo Kuen Lam8Department of Family Medicine and Primary Care The University of Hong Kong Hong Kong SAR ChinaDepartment of Family Medicine and Primary Care The University of Hong Kong Hong Kong SAR ChinaDepartment of Family Medicine and Primary Care The University of Hong Kong Hong Kong SAR ChinaMedical Research Council (MRC) Biostatistics Unit University of Cambridge Cambridge United KingdomCentre for Safe Medication Practice and Research Department of Pharmacology and Pharmacy The University of Hong Kong Hong Kong SAR ChinaCentre for Safe Medication Practice and Research Department of Pharmacology and Pharmacy The University of Hong Kong Hong Kong SAR ChinaCentre for Safe Medication Practice and Research Department of Pharmacology and Pharmacy The University of Hong Kong Hong Kong SAR ChinaDepartment of Family Medicine and Primary Care The University of Hong Kong Hong Kong SAR ChinaDepartment of Family Medicine and Primary Care The University of Hong Kong Hong Kong SAR ChinaBackground The detrimental effects of increased variability in systolic blood pressure (SBP) on cardiovascular disease (CVD) and mortality risk in patients with diabetes mellitus remains unclear. This study evaluated age‐specific association of usual SBP visit‐to‐visit variability with CVD and mortality in patients with type 2 diabetes mellitus. Methods and Results A retrospective cohort study investigated 155 982 patients with diabetes mellitus aged 45 to 84 years without CVD at baseline (2008–2010). Usual SBP variability was estimated using SBP SD obtained from a mixed‐effects model. Age‐specific associations (45–54, 55–64, 65–74, 75–84 years) between usual SBP variability, CVD, and mortality risk were assessed by Cox regression adjusted for patient characteristics. After a median follow‐up of 9.7 years, 49 816 events (including 34 039 CVD events and 29 211 mortalities) were identified. Elevated SBP variability was independently, positively, and log‐linearly associated with higher CVD and mortality risk among all age groups, with no evidence of any threshold effects. The excess CVD and mortality risk per 5 mm Hg increase in SBP variability within the 45 to 54 age group is >3 times higher than the 70 to 79 age group (hazard ratio, 1.66; 95% CI, 1.49–1.85 versus hazard ratio, 1.19; 95% CI, 1.15–1.23). The significant associations remained consistent among all subgroups. Patients with younger age had a higher association of SBP variability with event outcomes. Conclusions The findings suggest that SBP visit‐to‐visit variability was strongly associated with CVD and mortality with no evidence of a threshold effect in a population with diabetes mellitus. As well as controlling overall blood pressure levels, SBP visit‐to‐visit variability should be monitored and evaluated in routine practice, in particular for younger patients.https://www.ahajournals.org/doi/10.1161/JAHA.120.019026blood pressurecardiovascular diseasediabetes mellitusmortalityvisit‐to‐visit variability
spellingShingle Eric Yuk Fai Wan
Esther Yee Tak Yu
Weng Yee Chin
Jessica K. Barrett
Ian Chi Kei Wong
Esther Wai Yin Chan
Celine Sze Ling Chui
Shiqi Chen
Cindy Lo Kuen Lam
Age‐Specific Associations of Usual Blood Pressure Variability With Cardiovascular Disease and Mortality: 10‐Year Diabetes Mellitus Cohort Study
blood pressure
cardiovascular disease
diabetes mellitus
mortality
visit‐to‐visit variability
title Age‐Specific Associations of Usual Blood Pressure Variability With Cardiovascular Disease and Mortality: 10‐Year Diabetes Mellitus Cohort Study
title_full Age‐Specific Associations of Usual Blood Pressure Variability With Cardiovascular Disease and Mortality: 10‐Year Diabetes Mellitus Cohort Study
title_fullStr Age‐Specific Associations of Usual Blood Pressure Variability With Cardiovascular Disease and Mortality: 10‐Year Diabetes Mellitus Cohort Study
title_full_unstemmed Age‐Specific Associations of Usual Blood Pressure Variability With Cardiovascular Disease and Mortality: 10‐Year Diabetes Mellitus Cohort Study
title_short Age‐Specific Associations of Usual Blood Pressure Variability With Cardiovascular Disease and Mortality: 10‐Year Diabetes Mellitus Cohort Study
title_sort age specific associations of usual blood pressure variability with cardiovascular disease and mortality 10 year diabetes mellitus cohort study
topic blood pressure
cardiovascular disease
diabetes mellitus
mortality
visit‐to‐visit variability
url https://www.ahajournals.org/doi/10.1161/JAHA.120.019026
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