Association between renin–angiotensin–aldosterone system blockade and future osteoporotic fracture risk in hypertensive population A population-based cohort study in Taiwan

Tissue renin-angiotensin-aldosterone system (RAAS) activation in sites of osteoporosis had been demonstrated in animal studies; however, the possibility of RAAS blockade to prevent future osteoporotic fracture had rarely been verified in clinical studies. We Used the Taiwan Longitudinal Health insur...

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Published inMedicine (Baltimore) Vol. 96; no. 46; p. e8331
Main Authors Chen, Chang-I., Yeh, Jong-Shiuan, Tsao, Nai-Wen, Lin, Fen-Yen, Shih, Chun-Ming, Chiang, Kuang-Hsing, Kao, Yung-Ta, Fang, Yu-Ann, Tsai, Lung-Wen, Liu, Wen-Chi, Nakagami, Hironori, Morishita, Ryuichi, Kuo, Yi-Jie, Huang, Chun-Yao
Format Journal Article
LanguageEnglish
Published United States Wolters Kluwer Health 01.11.2017
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ISSN0025-7974
1536-5964
1536-5964
DOI10.1097/MD.0000000000008331

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Abstract Tissue renin-angiotensin-aldosterone system (RAAS) activation in sites of osteoporosis had been demonstrated in animal studies; however, the possibility of RAAS blockade to prevent future osteoporotic fracture had rarely been verified in clinical studies. We Used the Taiwan Longitudinal Health insurance database 2000 to 2008, the cohort study comprised patients age over 40 with a recorded new diagnosis of hypertension between January 1, 2000 to December 31, 2008, in addition, patients who had diagnosis of osteoporosis before the date of cohort enter were excluded. After the definite diagnosis of hypertension, each patient was followed until osteoporotic fracture happened or the end of 2008. The occurrence of osteoporotic fracture was evaluated in patients who either were or without taking RAAS blockade agents. Cox proportional hazard regressions were used to evaluate the osteoporotic fracture incidence after adjusting for known confounding factors. In total, 57,132 hypertensive patients comprised the study cohort. Our study results showed that the incidence of osteoporosis fracture in the whole cohort was significantly higher in the RAAS blockade non-user group than the user group. This phenomenon was observed in both sex and all age categories. Sensitivity analysis further showed the concordant lower osteoporosis fracture risk in patients with various RAAS blockers usage durations; the risk of osteoporosis fracture was the lowest in those drug use >365 days when compared with the non-user cohort. In conclusion, our study result demonstrated the lower future osteoporotic fracture risk in hypertensive subjects who received long term RAAS blocker treatment.
AbstractList Tissue renin–angiotensin–aldosterone system (RAAS) activation in sites of osteoporosis had been demonstrated in animal studies; however, the possibility of RAAS blockade to prevent future osteoporotic fracture had rarely been verified in clinical studies. We Used the Taiwan Longitudinal Health insurance database 2000 to 2008, the cohort study comprised patients age over 40 with a recorded new diagnosis of hypertension between January 1, 2000 to December 31, 2008, in addition, patients who had diagnosis of osteoporosis before the date of cohort enter were excluded. After the definite diagnosis of hypertension, each patient was followed until osteoporotic fracture happened or the end of 2008. The occurrence of osteoporotic fracture was evaluated in patients who either were or without taking RAAS blockade agents. Cox proportional hazard regressions were used to evaluate the osteoporotic fracture incidence after adjusting for known confounding factors. In total, 57,132 hypertensive patients comprised the study cohort. Our study results showed that the incidence of osteoporosis fracture in the whole cohort was significantly higher in the RAAS blockade non-user group than the user group. This phenomenon was observed in both sex and all age categories. Sensitivity analysis further showed the concordant lower osteoporosis fracture risk in patients with various RAAS blockers usage durations; the risk of osteoporosis fracture was the lowest in those drug use >365 days when compared with the non-user cohort. In conclusion, our study result demonstrated the lower future osteoporotic fracture risk in hypertensive subjects who received long term RAAS blocker treatment.
Tissue renin-angiotensin-aldosterone system (RAAS) activation in sites of osteoporosis had been demonstrated in animal studies; however, the possibility of RAAS blockade to prevent future osteoporotic fracture had rarely been verified in clinical studies. We Used the Taiwan Longitudinal Health insurance database 2000 to 2008, the cohort study comprised patients age over 40 with a recorded new diagnosis of hypertension between January 1, 2000 to December 31, 2008, in addition, patients who had diagnosis of osteoporosis before the date of cohort enter were excluded. After the definite diagnosis of hypertension, each patient was followed until osteoporotic fracture happened or the end of 2008. The occurrence of osteoporotic fracture was evaluated in patients who either were or without taking RAAS blockade agents. Cox proportional hazard regressions were used to evaluate the osteoporotic fracture incidence after adjusting for known confounding factors. In total, 57,132 hypertensive patients comprised the study cohort. Our study results showed that the incidence of osteoporosis fracture in the whole cohort was significantly higher in the RAAS blockade non-user group than the user group. This phenomenon was observed in both sex and all age categories. Sensitivity analysis further showed the concordant lower osteoporosis fracture risk in patients with various RAAS blockers usage durations; the risk of osteoporosis fracture was the lowest in those drug use >365 days when compared with the non-user cohort. In conclusion, our study result demonstrated the lower future osteoporotic fracture risk in hypertensive subjects who received long term RAAS blocker treatment.Tissue renin-angiotensin-aldosterone system (RAAS) activation in sites of osteoporosis had been demonstrated in animal studies; however, the possibility of RAAS blockade to prevent future osteoporotic fracture had rarely been verified in clinical studies. We Used the Taiwan Longitudinal Health insurance database 2000 to 2008, the cohort study comprised patients age over 40 with a recorded new diagnosis of hypertension between January 1, 2000 to December 31, 2008, in addition, patients who had diagnosis of osteoporosis before the date of cohort enter were excluded. After the definite diagnosis of hypertension, each patient was followed until osteoporotic fracture happened or the end of 2008. The occurrence of osteoporotic fracture was evaluated in patients who either were or without taking RAAS blockade agents. Cox proportional hazard regressions were used to evaluate the osteoporotic fracture incidence after adjusting for known confounding factors. In total, 57,132 hypertensive patients comprised the study cohort. Our study results showed that the incidence of osteoporosis fracture in the whole cohort was significantly higher in the RAAS blockade non-user group than the user group. This phenomenon was observed in both sex and all age categories. Sensitivity analysis further showed the concordant lower osteoporosis fracture risk in patients with various RAAS blockers usage durations; the risk of osteoporosis fracture was the lowest in those drug use >365 days when compared with the non-user cohort. In conclusion, our study result demonstrated the lower future osteoporotic fracture risk in hypertensive subjects who received long term RAAS blocker treatment.
Author Morishita, Ryuichi
Tsai, Lung-Wen
Fang, Yu-Ann
Lin, Fen-Yen
Nakagami, Hironori
Shih, Chun-Ming
Chiang, Kuang-Hsing
Tsao, Nai-Wen
Liu, Wen-Chi
Chen, Chang-I.
Kuo, Yi-Jie
Yeh, Jong-Shiuan
Huang, Chun-Yao
Kao, Yung-Ta
AuthorAffiliation l Cancer Center, Taipei Medical University Wang Fung Hospital
j Department of Surgery, Taipei Medical University Hospital
k Division of Cardiology
f Graduate Institute of Biomedical Informatics, Taipei Medical University
a Department of Internal Medicine
m Institute of Clinical Medical Sciences, Chang Gung University
b Department of Surgery
d School of Health Care Administration
o Department of Health Development and Medicine
p Department of Clinical Gene Medicine, Osaka University, Osaka, Japan
g Division of Cardiology and Cardiovascular Research Center
h Evidence-base Medicine Center
i Department of Business
e Center of Excellence for Cancer Research
c Graduate Institute of Clinical Medicine, School of Medicine, College of Medicine
n Department of Living Science, National Open University, Taipei, Taiwan
AuthorAffiliation_xml – name: k Division of Cardiology
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– name: m Institute of Clinical Medical Sciences, Chang Gung University
– name: p Department of Clinical Gene Medicine, Osaka University, Osaka, Japan
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Snippet Tissue renin-angiotensin-aldosterone system (RAAS) activation in sites of osteoporosis had been demonstrated in animal studies; however, the possibility of...
Tissue renin–angiotensin–aldosterone system (RAAS) activation in sites of osteoporosis had been demonstrated in animal studies; however, the possibility of...
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SubjectTerms Aged
Antihypertensive Agents - pharmacology
Antihypertensive Agents - therapeutic use
Cohort Studies
Female
Humans
Hypertension - drug therapy
Male
Middle Aged
Observational Study
Osteoporotic Fractures - epidemiology
Osteoporotic Fractures - prevention & control
Renin-Angiotensin System - drug effects
Taiwan - epidemiology
Subtitle A population-based cohort study in Taiwan
Title Association between renin–angiotensin–aldosterone system blockade and future osteoporotic fracture risk in hypertensive population
URI https://www.ncbi.nlm.nih.gov/pubmed/29145244
https://www.proquest.com/docview/1966232103
https://pubmed.ncbi.nlm.nih.gov/PMC5704789
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