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 in | Medicine (Baltimore) Vol. 96; no. 46; p. e8331 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
Wolters Kluwer Health
01.11.2017
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ISSN | 0025-7974 1536-5964 1536-5964 |
DOI | 10.1097/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. |
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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 – name: h Evidence-base Medicine Center – name: b Department of Surgery – name: c Graduate Institute of Clinical Medicine, School of Medicine, College of Medicine – name: l Cancer Center, Taipei Medical University Wang Fung Hospital – name: j Department of Surgery, Taipei Medical University Hospital – name: o Department of Health Development and Medicine – name: m Institute of Clinical Medical Sciences, Chang Gung University – name: p Department of Clinical Gene Medicine, Osaka University, Osaka, Japan – name: d School of Health Care Administration – name: f Graduate Institute of Biomedical Informatics, Taipei Medical University – name: e Center of Excellence for Cancer Research – name: a Department of Internal Medicine – name: g Division of Cardiology and Cardiovascular Research Center – name: i Department of Business – name: n Department of Living Science, National Open University, Taipei, Taiwan |
Author_xml | – sequence: 1 givenname: Chang-I. surname: Chen fullname: Chen, Chang-I. – sequence: 2 givenname: Jong-Shiuan surname: Yeh fullname: Yeh, Jong-Shiuan – sequence: 3 givenname: Nai-Wen surname: Tsao fullname: Tsao, Nai-Wen – sequence: 4 givenname: Fen-Yen surname: Lin fullname: Lin, Fen-Yen – sequence: 5 givenname: Chun-Ming surname: Shih fullname: Shih, Chun-Ming – sequence: 6 givenname: Kuang-Hsing surname: Chiang fullname: Chiang, Kuang-Hsing – sequence: 7 givenname: Yung-Ta surname: Kao fullname: Kao, Yung-Ta – sequence: 8 givenname: Yu-Ann surname: Fang fullname: Fang, Yu-Ann – sequence: 9 givenname: Lung-Wen surname: Tsai fullname: Tsai, Lung-Wen – sequence: 10 givenname: Wen-Chi surname: Liu fullname: Liu, Wen-Chi – sequence: 11 givenname: Hironori surname: Nakagami fullname: Nakagami, Hironori – sequence: 12 givenname: Ryuichi surname: Morishita fullname: Morishita, Ryuichi – sequence: 13 givenname: Yi-Jie surname: Kuo fullname: Kuo, Yi-Jie – sequence: 14 givenname: Chun-Yao surname: Huang fullname: Huang, Chun-Yao |
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CitedBy_id | crossref_primary_10_1007_s11657_021_01004_6 crossref_primary_10_1007_s00198_019_05041_3 crossref_primary_10_1016_j_spinee_2019_04_017 crossref_primary_10_1002_jcb_30069 crossref_primary_10_1016_j_ijcard_2019_12_069 crossref_primary_10_3389_fphys_2022_1037750 crossref_primary_10_1007_s00223_022_01004_9 crossref_primary_10_1016_j_bone_2020_115477 crossref_primary_10_1186_s12891_023_07102_5 |
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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 |
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