共 49 条
Association between BMD and coronary artery calcification: an observational and Mendelian randomization study
被引:3
作者:
Lu, Haojie
[1
,2
]
Lary, Christine W.
[3
]
Hodonsky, Chani J.
[4
]
Peyser, Patricia A.
[5
]
Bos, Daniel
[6
]
van der Laan, Sander W.
[7
]
Miller, Clint L.
[4
,8
,9
]
Rivadeneira, Fernando
[2
]
Kiel, Douglas P.
[10
,11
]
Kavousi, Maryam
[1
]
Medina-Gomez, Carolina
[2
]
机构:
[1] Univ Med Ctr Rotterdam, Dept Epidemiol, Erasmus MC, NL-3000 CA Rotterdam, Netherlands
[2] Univ Med Ctr, Dept Internal Med, Erasmus MC, Postbus 2040, NL-CA 3000 Rotterdam, Netherlands
[3] Northeastern Univ, Roux Inst, Portland, ME 04101 USA
[4] Univ Virginia, Ctr Publ Hlth Genom, Charlottesville, VA 22903 USA
[5] Univ Michigan, Sch Publ Hlth, Dept Epidemiol, Ann Arbor, MI 48109 USA
[6] Erasmus MC, Univ Med Ctr Rotterdam, Dept Radiol & Nucl Med, NL-3000 CA Rotterdam, Netherlands
[7] Univ Med Ctr Utrecht, Utrecht Univ, Div Labs Pharm & Biomed Genet, Cent Diagnost Lab, NL-CX 3584 Utrecht, Netherlands
[8] Univ Virginia, Dept Biochem & Mol Genet, Charlottesville, VA 22903 USA
[9] Univ Virginia, Dept Publ Hlth Sci, Charlottesville, VA 22903 USA
[10] Hebrew SeniorLife, Hinda & Arthur Marcus Inst Aging Res, Boston, MA 02131 USA
[11] Beth Israel Deaconess Med Ctr, Harvard Med Sch, Dept Med, Boston, MA 02215 USA
关键词:
Mendelian randomization;
polygenic risk score;
BMD;
osteoporosis;
coronary artery calcification;
BONE-MINERAL DENSITY;
VASCULAR CALCIFICATION;
RISK-FACTORS;
OSTEOPOROSIS;
INSTRUMENTS;
METAANALYSIS;
CALCIUM;
HEART;
POWER;
BIAS;
D O I:
10.1093/jbmr/zjae022
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Observational studies have reported inconsistent associations between bone mineral density (BMD) and coronary artery calcification (CAC). We examined the observational association of BMD with CAC in 2 large population-based studies and evaluated the evidence for a potential causal relation between BMD and CAC using polygenic risk scores (PRS), 1- and 2-sample Mendelian randomization (MR) approaches. Our study populations comprised 1414 individuals (mean age 69.9 yr, 52.0% women) from the Rotterdam Study and 2233 individuals (mean age 56.5 yr, 50.9% women) from the Framingham Heart Study with complete information on CAC and BMD measurements at the total body (TB-), lumbar spine (LS-), and femoral neck (FN-). We used linear regression models to evaluate the observational association between BMD and CAC. Subsequently, we compared the mean CAC across PRSBMD quintile groups at different skeletal sites. In addition, we used the 2-stage least squares regression and the inverse variance weighted (IVW) model as primary methods for 1- and 2-sample MR to test evidence for a potentially causal association. We did not observe robust associations between measured BMD levels and CAC. These results were consistent with a uniform random distribution of mean CAC across PRSBMD quintile groups (P-value > .05). Moreover, neither 1- nor 2-sample MR supported the possible causal association between BMD and CAC. Our results do not support the contention that lower BMD is (causally) associated with an increased CAC risk. These findings suggest that previously reported epidemiological associations of BMD with CAC are likely explained by unmeasured confounders or shared etiology, rather than by causal pathways underlying both osteoporosis and vascular calcification processes.
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页码:443 / 452
页数:10
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