Low bone mineral density is associated with coronary arterial calcification progression and incident cardiovascular events in patients with chronic kidney disease

被引:13
|
作者
Kim, Hyoungnae [1 ]
Lee, Joongyub [2 ]
Lee, Kyu-Beck [3 ]
Kim, Yeong-Hoon [4 ]
Hong, Namki [5 ]
Park, Jung Tak [6 ]
Han, Seung Hyeok [6 ]
Kang, Shin-Wook [6 ]
Choi, Kyu Hun [6 ]
Oh, Kook-Hwan [7 ]
Yoo, Tae-Hyun [6 ]
机构
[1] Soonchunhyang Univ, Div Nephrol, Seoul Hosp, Seoul, South Korea
[2] Inha Univ Hosp, Prevent & Management Ctr, Incheon, South Korea
[3] Sungkyunkwan Univ, Kangbuk Samsung Hosp, Dept Internal Med, Sch Med, Seoul, South Korea
[4] Inje Univ, Busan Paik Hosp, Coll Med, Dept Internal Med, Busan, South Korea
[5] Yonsei Univ, Dept Internal Med, Div Endocrinol & Metab, Coll Med, Seoul, South Korea
[6] Yonsei Univ, Coll Med, Inst Kidney Dis Res, Dept Internal Med, Seoul, South Korea
[7] Seoul Natl Univ, Dept Internal Med, Coll Med, Seoul, South Korea
关键词
bone mineral density; cardiovascular disease; chronic kidney disease; coronary calcification; osteoporosis; RENAL OSTEODYSTROPHY; BIOCHEMICAL MARKERS; ALL-CAUSE; RISK; OSTEOPOROSIS; MORTALITY; FRACTURE; DEATH; PREDICTOR; TURNOVER;
D O I
10.1093/ckj/sfab138
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background. Although it is well known that low bone mineral density (BMD) is associated with an increased risk of cardiovascular disease (CVD) and mortality in the general population, the prognostic role of bone mineral density (BMD) has not been established in the chronic kidney disease (CKD) population. Therefore we aimed to evaluate the association between BMD and the risk of CVD and cardiovascular mortality in patients with predialysis CKD. Methods. This prospective cohort study was conducted with 1957 patients with predialysis CKD Stages 1-5. BMD was measured using dual-energy X-ray absorptiometry and coronary arterial calcification (CAC) scores were evaluated using coronary computed tomography. The primary outcome was a major adverse cardiovascular event (MACE). Results. When patients were classified based on total hip BMD T-score tertiles stratified by sex, the lowest BMD tertile was significantly associated with an increased risk of MACE fhazard ratio 2.16 [95% confidence interval (CI) 1.25-3.74]; P = 0.006g. This association was also shown with BMD at the femur neck but not with BMD at lumbar spine. In the subgroup of 977 patients with follow-up CACs at their fourth year, 97 (9.9%) showed accelerated CAC progression (>50/year), and BMD was inversely associated with accelerated CAC progression even after adjusting for the baseline CAC score [odds ratio 0.75 (95% CI 0.58-0.99); P = 0.039]. In addition, baseline CAC was associated with an increased risk of MACEs after adjusting for total hip T-score. Conclusions. Low BMD was significantly associated with CAC progression and MACEs in patients with predialysis CKD.
引用
收藏
页码:119 / 127
页数:9
相关论文
共 50 条
  • [31] BONE MINERAL DENSITY AND ADEQUACY OF DIETARY PATTERN OF PATIENTS WITH CHRONIC KIDNEY DISEASE IN HEMODIALYSIS
    Carrasco, Fernando
    Cano, Marcelo
    Camousseigt, Jean
    Rojas, Pamela
    Inostroza, Jorge
    Torres, Ruben
    NUTRICION HOSPITALARIA, 2013, 28 (04) : 1306 - 1312
  • [32] Coronary artery calcification and cardiovascular disease in children with chronic kidney disease
    Paoli, Sara
    Mitsnefes, Mark M.
    CURRENT OPINION IN PEDIATRICS, 2014, 26 (02) : 193 - 197
  • [33] Effect of Intravenous Contrast on Volumetric Bone Mineral Density in Patients with Chronic Kidney Disease
    Jorgensen, Hanne Skou
    Winther, Simon
    Bottcher, Morten
    Thygesen, Jesper
    Rejnmark, Lars
    Hauge, Ellen-Margrethe
    Svensson, My
    Ivarsen, Per
    JOURNAL OF CLINICAL DENSITOMETRY, 2016, 19 (04) : 423 - 429
  • [34] Bone microarchitecture and estimated failure load are deteriorated whether patients with chronic kidney disease have normal bone mineral density, osteopenia or osteoporosis
    Ghasem-Zadeh, Ali
    Bui, Minh
    Seeman, Ego
    Boyd, Steven K.
    Iuliano, Sandra
    Jaipurwala, Rizwan
    Mount, Peter F.
    Toussaint, Nigel D.
    Chiang, Cherie
    BONE, 2022, 154
  • [35] Low bone mineral density is associated with increased arterial stiffness in participants of a health records based study
    Wang, Ya-Qin
    Yang, Ping-Ting
    Yuan, Hong
    Cao, Xia
    Zhu, Xiao-Ling
    Xu, Guo
    Mo, Zhao-Hui
    Chen, Zhi-Heng
    JOURNAL OF THORACIC DISEASE, 2015, 7 (05) : 790 - 798
  • [36] Low bone mineral density is associated with global coronary atherosclerotic plaque burden in stable angina patients
    Guan, Xue-qiang
    Xue, Yang-jing
    Wang, Jie
    Ma, Jun
    Li, Yue-chun
    Zheng, Cheng
    Wu, Sai-zhu
    CLINICAL INTERVENTIONS IN AGING, 2018, 13 : 1475 - 1483
  • [37] Low bone mineral density in adult patients with coeliac disease
    Szymczak, Jadwiga
    Bohdanowicz-Pawlak, Anna
    Waszczuk, Ewa
    Jakubowska, Joanna
    ENDOKRYNOLOGIA POLSKA, 2012, 63 (04) : 270 - 276
  • [38] Association of Body Weight Variability With Progression of Coronary Artery Calcification in Patients With Predialysis Chronic Kidney Disease
    Suh, Sang Heon
    Oh, Tae Ryom
    Choi, Hong Sang
    Kim, Chang Seong
    Bae, Eun Hui
    Oh, Kook-Hwan
    Lee, Kyu-Beck
    Han, Seung Hyeok
    Sung, Suah
    Ma, Seong Kwon
    Kim, Soo Wan
    FRONTIERS IN CARDIOVASCULAR MEDICINE, 2022, 8
  • [39] Severe Coronary Artery Calcifications in Chronic Kidney Disease Patients, Coupled with Inflammation and Bone Mineral Disease Derangement, Promote Major Adverse Cardiovascular Events through Vascular Remodeling
    Morena-Carrere, Marion
    Jaussent, Isabelle
    Chenine, Leila
    Dupuy, Anne-Marie
    Bargnoux, Anne-Sophie
    Leray-Moragues, Helene
    Klouche, Kada
    Vernhet, Helene
    Canaud, Bernard
    Cristol, Jean-Paul
    KIDNEY & BLOOD PRESSURE RESEARCH, 2025, 50 (01) : 33 - 45
  • [40] Development of a novel chronic kidney disease mouse model to evaluate the progression of hyperphosphatemia and associated mineral bone disease
    Tani, Takashi
    Orimo, Hideo
    Shimizu, Akira
    Tsuruoka, Shuichi
    SCIENTIFIC REPORTS, 2017, 7