UMMS Affiliation
Department of Medicine, Division of Clinical Informatics; UMass Worcester Prevention Research Center
Publication Date
2019-04-24
Document Type
Article
Disciplines
Amino Acids, Peptides, and Proteins | Clinical Epidemiology | Epidemiology | Fluids and Secretions | Hemic and Immune Systems | Musculoskeletal, Neural, and Ocular Physiology | Musculoskeletal System | Women's Health
Abstract
OBJECTIVES: Elevated Lipoprotein(a) (Lp[a]) is a well-known risk factor for cardiovascular disease. However, its roles in bone metabolism and fracture risk are unclear. We therefore investigated whether plasma Lp(a) levels were associated with bone mineral density (BMD) and incident hip fractures in a large cohort of postmenopausal women.
DESIGN: Post hoc analysis of data from the Women's Health Initiative (WHI), USA.
SETTING: 40 clinical centres in the USA.
PARTICIPANTS: The current analytical cohort consisted of 9698 white, postmenopausal women enrolled in the WHI, a national prospective study investigating determinants of chronic diseases including heart disease, breast and colorectal cancers and osteoporotic fractures among postmenopausal women. Recruitment for WHI took place from 1 October 1993 to 31 December 1998.
EXPOSURES: Plasma Lp(a) levels were measured at baseline.
OUTCOME MEASURES: Incident hip fractures were ascertained annually and confirmed by medical records with follow-up through 29 August 2014. BMD at the femoral neck was measured by dual X-ray absorptiometry in a subset of participants at baseline.
STATISTICAL ANALYSES: Cox proportional hazards and logistic regression models were used to evaluate associations of quartiles of plasma Lp(a) levels with hip fracture events and hip BMD T-score, respectively.
RESULTS: During a mean follow-up of 13.8 years, 454 incident cases of hip fracture were observed. In analyses adjusting for confounding variables including age, body mass index, history of hysterectomy, smoking, physical activity, diabetes mellitus, general health status, cardiovascular disease, use of menopausal hormone therapy, use of bisphosphonates, calcitonin or selective-oestrogen receptor modulators, baseline dietary and supplemental calcium and vitamin D intake and history of fracture, no significant association of plasma Lp(a) levels with low hip BMD T-score or hip fracture risk was detected.
CONCLUSIONS: These findings suggest that plasma Lp(a) levels are not related to hip BMD T-score or hip fracture events in postmenopausal women.
TRIAL REGISTRATION NUMBER: NCT00000611; Post-results.
Keywords
bone mineral density, fractures, lipoprotein (a), postmenopausal women
Rights and Permissions
Copyright © Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
DOI of Published Version
10.1136/bmjopen-2018-027257
Source
BMJ Open. 2019 Apr 24;9(4):e027257. doi: 10.1136/bmjopen-2018-027257. Link to article on publisher's site
Journal/Book/Conference Title
BMJ open
Related Resources
PubMed ID
31023762
Repository Citation
Haring, Bernhard; Crandall, Carolyn J.; Carbone, Laura; Liu, Simin; Li, Wenjun; Johnson, Karen C.; Wactawski-Wende, Jean; Shadyab, Aladdin H.; Gass, Margery L.; Kamensky, Victor; Cauley, Jane A.; and Wassertheil-Smoller, Sylvia, "Lipoprotein(a) plasma levels, bone mineral density and risk of hip fracture: a post hoc analysis of the Women's Health Initiative, USA" (2019). Open Access Articles. 3817.
https://escholarship.umassmed.edu/oapubs/3817
Creative Commons License
This work is licensed under a Creative Commons Attribution-Noncommercial 4.0 License
Included in
Amino Acids, Peptides, and Proteins Commons, Clinical Epidemiology Commons, Epidemiology Commons, Fluids and Secretions Commons, Hemic and Immune Systems Commons, Musculoskeletal, Neural, and Ocular Physiology Commons, Musculoskeletal System Commons, Women's Health Commons