TY - JOUR
T1 - Bone mineral density and long-term progression of aortic valve and mitral annular calcification
T2 - The Multi-Ethnic Study of Atherosclerosis
AU - Massera, Daniele
AU - Buzkova, Petra
AU - Bortnick, Anna E.
AU - Owens, David S.
AU - Mao, Song Shou
AU - Li, Dong
AU - De Boer, Ian H.
AU - Kestenbaum, Bryan R.
AU - Budoff, Matthew J.
AU - Kizer, Jorge
N1 - Funding Information:
This research was supported by contracts HHSN268201500003I , N01-HC-95159 , N01-HC-95160 , N01-HC-95161 , N01-HC-95162 , N01-HC-95163 , N01-HC-95164 , N01-HC-95165 , N01-HC-95166 , N01-HC-95167 , N01-HC-95168 , N01-HC-95169 and grants R01HL096875 and R01HL071739 from the National Heart, Lung, and Blood Institute , by grants UL1-TR-000040 , UL1-TR-001079 , and UL1-TR-001420 from the National Center for Advancing Translational Sciences (NCATS) and by grant 2R42AR070713-02A1 from the National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) .
Funding Information:
This research was supported by contracts HHSN268201500003I, N01-HC-95159, N01-HC-95160, N01-HC-95161, N01-HC-95162, N01-HC-95163, N01-HC-95164, N01-HC-95165, N01-HC-95166, N01-HC-95167, N01-HC-95168, N01-HC-95169 and grants R01HL096875 and R01HL071739 from the National Heart, Lung, and Blood Institute, by grants UL1-TR-000040, UL1-TR-001079, and UL1-TR-001420 from the National Center for Advancing Translational Sciences (NCATS) and by grant 2R42AR070713-02A1 from the National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS).This publication was developed under a STAR research assistance agreements, No. RD831697 (MESA Air) and RD-83830001 (MESA Air Next Stage), awarded by the U.S. Environmental Protection Agency. It has not been formally reviewed by the EPA. The views expressed in this document are solely those of the authors and the EPA does not endorse any products or commercial services mentioned in this publication.AEB was supported by American Heart Association Mentored and Clinical Population Research Award 17MCPRP33630098 and K23 HL146982 from the National Heart, Lung, and Blood Institute; JRK was supported by K24 Hl135413 from the National Heart, Lung, and Blood Institute.DM received consulting fees from Bristol Myers Squibb. AEB served as site principal investigator for multi-center trials sponsored by Abbott and CSL-Behring for which her institution received compensation. JRK reports stock ownership in Abbott, Bristol Myers Squibb, Johnson & Johnson, Medtronic, Merck and Pfizer. All other authors declare that they have no conflicts of interest.
Funding Information:
AEB was supported by American Heart Association Mentored and Clinical Population Research Award 17MCPRP33630098 and K23 HL146982 from the National Heart, Lung, and Blood Institute; JRK was supported by K24 Hl135413 from the National Heart, Lung, and Blood Institute .
Publisher Copyright:
© 2021 Elsevier B.V.
PY - 2021/10
Y1 - 2021/10
N2 - Background and aims: Bone and mineral metabolism has been implicated in the pathophysiology of cardiac valve calcification. Whether bone demineralization, a common aging-related disorder, promotes calcific valve disease remains uncertain. We tested the hypothesis that low bone mineral density (BMD) is associated with greater incidence/progression of cardiac valve calcification in the Multi-Ethnic Study of Atherosclerosis. Methods: Using linear mixed-effects models, we related baseline measurement of BMD of the thoracic vertebrae by computed tomography (CT) in 6768 participants to serial CT assessments of aortic valve calcification (AVC) and mitral annular calcification (MAC) obtained over a >10-year period. Results: After multivariable adjustment, lower BMD (per SD decrement) was associated with accelerated increase in AVC over time in women (0.76 [95% CI 0.42,1.09] Agatston -units [AU]/year) and men (1.41 [95% CI 0.48,2.33] AU/year), as well as for MAC in women (3.22 [95% CI 1.16,5.28] AU/year) and men (3.59 [95% CI 2.09,5.09] AU/year). Significant effect modification was observed, with more pronounced BMD-related acceleration of AVC and MAC progression in older or white participants of one or both sexes, as well as by estimated glomerular filtration rate, though the latter differed by sex for AVC and MAC. Conclusions: In this multi-ethnic cohort, low thoracic BMD was significantly, but modestly, associated with increased AVC and MAC progression. This suggests that altered bone mineral metabolism does not have a major impact on calcific valve disease in the general population, but the possibility of a more meaningful influence in higher-risk individuals with osteoporosis will require further investigation.
AB - Background and aims: Bone and mineral metabolism has been implicated in the pathophysiology of cardiac valve calcification. Whether bone demineralization, a common aging-related disorder, promotes calcific valve disease remains uncertain. We tested the hypothesis that low bone mineral density (BMD) is associated with greater incidence/progression of cardiac valve calcification in the Multi-Ethnic Study of Atherosclerosis. Methods: Using linear mixed-effects models, we related baseline measurement of BMD of the thoracic vertebrae by computed tomography (CT) in 6768 participants to serial CT assessments of aortic valve calcification (AVC) and mitral annular calcification (MAC) obtained over a >10-year period. Results: After multivariable adjustment, lower BMD (per SD decrement) was associated with accelerated increase in AVC over time in women (0.76 [95% CI 0.42,1.09] Agatston -units [AU]/year) and men (1.41 [95% CI 0.48,2.33] AU/year), as well as for MAC in women (3.22 [95% CI 1.16,5.28] AU/year) and men (3.59 [95% CI 2.09,5.09] AU/year). Significant effect modification was observed, with more pronounced BMD-related acceleration of AVC and MAC progression in older or white participants of one or both sexes, as well as by estimated glomerular filtration rate, though the latter differed by sex for AVC and MAC. Conclusions: In this multi-ethnic cohort, low thoracic BMD was significantly, but modestly, associated with increased AVC and MAC progression. This suggests that altered bone mineral metabolism does not have a major impact on calcific valve disease in the general population, but the possibility of a more meaningful influence in higher-risk individuals with osteoporosis will require further investigation.
KW - Aortic valve calcification
KW - Bone mineral density
KW - Epidemiology
KW - Mitral annular calcification
UR - http://www.scopus.com/inward/record.url?scp=85114689059&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85114689059&partnerID=8YFLogxK
U2 - 10.1016/j.atherosclerosis.2021.08.031
DO - 10.1016/j.atherosclerosis.2021.08.031
M3 - Article
C2 - 34511241
AN - SCOPUS:85114689059
SN - 0021-9150
VL - 335
SP - 126
EP - 134
JO - Atherosclerosis
JF - Atherosclerosis
ER -