Abstract
Summary
Accurate patient risk perception of adverse health events promotes greater autonomy over, and motivation towards, health-related lifestyles.
Introduction
We compared self-perceived fracture risk and 3-year incident fracture rates in postmenopausal women with a range of morbidities in the Global Longitudinal study of Osteoporosis in Women (GLOW).
Methods
GLOW is an international cohort study involving 723 physician practices across ten countries (Europe, North America, Australasia); 60,393 women aged ≥55 years completed baseline questionnaires detailing medical history and self-perceived fracture risk. Annual follow-up determined self-reported incident fractures.
Results
In total 2,945/43,832 (6.8 %) sustained an incident fracture over 3 years. All morbidities were associated with increased fracture rates, particularly Parkinson's disease (hazard ratio [HR]; 95 % confidence interval [CI], 3.89; 2.78–5.44), multiple sclerosis (2.70; 1.90–3.83), cerebrovascular events (2.02; 1.67–2.46), and rheumatoid arthritis (2.15; 1.53–3.04) (all p < 0.001). Most individuals perceived their fracture risk as similar to (46 %) or lower than (36 %) women of the same age. While increased self-perceived fracture risk was strongly associated with incident fracture rates, only 29 % experiencing a fracture perceived their risk as increased. Under-appreciation of fracture risk occurred for all morbidities, including neurological disease, where women with low self-perceived fracture risk had a fracture HR 2.39 (CI 1.74–3.29) compared with women without morbidities.
Conclusions
Postmenopausal women with morbidities tend to under-appreciate their risk, including in the context of neurological diseases, where fracture rates were highest in this cohort. This has important implications for health education, particularly among women with Parkinson's disease, multiple sclerosis, or cerebrovascular disease.
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Acknowledgments
We thank the physicians, project coordinators, and women participating in GLOW.
Funding
Funding/Support and Role of the Sponsor: Financial support for the GLOW study is provided by Warner Chilcott Company, LLC and sanofi-aventis to the Center for Outcomes Research, University of Massachusetts Medical School. The sponsors had no involvement in the design and conduct of the study; collection, management, analysis, and interpretation of the data; or preparation, review, or approval of the manuscript. The design, conduct, and interpretation of the GLOW data are undertaken by an independent steering committee. The Medical Research Council and the University of Southampton provided funding infrastructure support for manuscript completion.
Conflicts of interest
CLG has no disclosures. EMD has no disclosures. JEC has undertaken paid consultancy work for Servier, Shire, Nycomed, Novartis, Amgen, Procter & Gamble, Wyeth, Pfizer, The Alliance for Better Bone Health, Roche, and GlaxoSmithKline; has been a paid speaker for and received reimbursement, travel and accommodation from Servier, Procter & Gamble, and Lilly; and has received research grants from Servier R&D and Procter & Gamble. SA has received speaker honoraria from Eli Lilly and Amgen; and consultancy honoraria from MSD, Eli Lilly, Amgen and Novartis. JDA has been a consultant/speaker for Amgen, Lilly, GlaxoSmithKline, Merck, Novartis, Nycomed, Pfizer, Procter & Gamble, Roche, sanofi-aventis, Servier, Warner Chilcott and Wyeth; and has conducted clinical trials for Amgen, Lilly, GlaxoSmithKline, Merck, Novartis, Pfizer, Procter & Gamble, Roche, sanofi-aventis, Warner Chilcott, Wyeth, and Bristol-Myers Squibb. FAA has received funding from The Alliance for Better Bone Health (sanofi-aventis and Warner Chilcott). SB has received research grants from Amgen, Lilly, Novartis, Pfizer, Procter & Gamble, sanofi-aventis, Roche, and GlaxoSmithKline; and has received honoraria from, served on Speakers' Bureaus for, and acted as a consultant/Advisory Board member for Amgen, Lilly, Merck, Novartis, Procter & Gamble, sanofi-aventis, and Servier. RC has received funding from the French Ministry of Health, Merck, Servier, Lilly, and Procter & Gamble; has received honoraria from Amgen, Servier, Novartis, Lilly, Roche, and sanofi-aventis; and has acted as a consultant/Advisory Board member for Amgen, Merck, Servier, Nycomed, and Novartis. AD-P has received consulting fees and lectured for Eli Lilly, Amgen, Procter & Gamble, Servier, and Daiichi-Sankyo; has been an expert witness for Merck; and is a consultant/Advisory Board member for Novartis, Eli Lilly, Amgen, and Procter & Gamble; has received honoraria from Novartis, Lilly, Amgen, Procter & Gamble, and Roche; has been an expert witness for Merck; and has acted as a consultant/Advisory Board member for Novartis, Lilly, Amgen, and Procter & Gamble. SLG has acted as a consultant/Advisory Board member for Amgen, Lilly, and Merck; and has received research grants from The Alliance for Better Bone Health (sanofi-aventis and Proctor & Gamble) and Lilly. FHH has received funding from The Alliance for Better Bone Health (sanofi-aventis and Warner Chilcott). AZL has received funding from The Alliance for Better Bone Health (sanofi-aventis and Warner Chilcott) and is an Advisory Board member for Amgen. JWN has no disclosures. JCN has undertaken paid consultancy work for Roche Diagnostics, Daiichi-Sankyo, Proctor & Gamble, and Nycomed; has been a paid speaker for and received reimbursement, travel and accommodation from Roche Diagnostics, Novartis, Daiichi-Sankyo, and Procter & Gamble; and has received research grants from The Alliance for Better Bone Health and Amgen. JP has received research grants from Amgen, Kyphon, Novartis, and Roche; has received other research support (equipment) from GE Lunar; has served on Speakers' Bureaus for Amgen, sanofi-aventis, GlaxoSmithKline, Roche, Lilly Deutschland, Orion Pharma, Merck, Merckle, Nycomed, and Procter & Gamble; and has acted as an Advisory Board member for Novartis, Roche, Procter & Gamble, and Teva. MR is on the Speakers' Bureau for Roche. CR has received honoraria from and acted as a consultant/Advisory Board member for Alliance, Amgen, Lilly, Merck, Novartis, Nycomed, Roche, GlaxoSmithKline, Servier, and Wyeth. KGS received consulting fees or other remuneration from Eli Lilly & Co, Merck, Novartis, and Amgen; and has conducted paid research for Eli Lilly & Co, Merck, Novartis, and Amgen. SS has received research grants from Wyeth, Lilly, Novartis, and Alliance; has served on Speakers' Bureaus for Lilly, Novartis, Pfizer, and Procter & Gamble; has received honoraria from Procter & Gamble; and has acted as a consultant/Advisory Board member for Lilly, Argen, Wyeth, Merck, Roche, and Novartis. ESS has acted as a consultant for Amgen, Lilly, Novartis, and The Alliance for Better Bone Health; and has served on Speakers' Bureaus in the past year for Amgen, and Lilly. NBW has received honoraria for lectures in the past year from Amgen, Novartis, and Warner Chilcott; has acted as a consultant in the past year for Amgen, Arena, Baxter, InteKrin, Johnson & Johnson, Lilly, Medpace, Merck, NPS, Orexigen, Pfizer/Wyeth, Takeda, Vivus, Warner Chilcott; has received research support (through University) from Amgen, Merck, and NPS; and co-founded, has stock options and is a director of OsteoDynamics. AW has no disclosures. CC has received consulting fees from and lectured for Amgen, The Alliance for Better Bone Health (sanofi-aventis and Warner Chilcott), Lilly, Merck, Servier, Novartis, and Roche-GSK.
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Table S1
Age-adjusted Kaplan–Meier 3-year hazard ratios for fracture by morbidities and self-perceived fracture risk (DOC 43 kb)
Table S2
Unadjusted Kaplan–Meier 3-year incident fracture rate estimates according to the cumulative morbidity index and grouped morbidities, stratified by self-perceived fracture risk (DOC 41 kb)
Table S3
Age-adjusted Kaplan–Meier 3-year hazard ratios according to morbidity, by self-perceived fracture risk (DOC 36 kb)
Table S4
Age-adjusted Kaplan–Meier 3-year hazard ratios according to morbidity index and grouped morbidities, by self-perceived fracture risk (DOC 35 kb)
Table S5
Potential influences on self-perceived fracture risk in postmenopausal women (DOC 49 kb)
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Gregson, C.L., Dennison, E.M., Compston, J.E. et al. Disease-specific perception of fracture risk and incident fracture rates: GLOW cohort study. Osteoporos Int 25, 85–95 (2014). https://doi.org/10.1007/s00198-013-2438-y
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DOI: https://doi.org/10.1007/s00198-013-2438-y