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Trends in statin prescription among osteoporosis patients: A retrospective cohort study using UK primary care data
Ingrid Mei-Fung Wong1, Philip Chun-Ming Au2, Noel Cassandra Yue2
1Department of Health Policy and Management, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, United States of America.
Insights
Statin prescribing for osteoporosis patients declined, especially in males, indicating potential gaps in cardiovascular care. Guidelines may influence these trends, but adherence remains a challenge for this multimorbid population.
Area of Science:
- Cardiology
- Geriatrics
- Pharmacology
Background:
- Cardiovascular disease is a major cause of death in osteoporosis patients.
- Statin prescribing patterns in this population are not well understood.
- Understanding these trends is crucial for improving patient outcomes.
Purpose of the Study:
- To examine temporal trends in statin prescription rates among osteoporosis patients in the UK.
- To analyze demographic variations (age, gender) in statin prescribing.
- To identify factors influencing these prescribing patterns.
Main Methods:
- Retrospective cohort study using IQVIA Medical Research Data (2005-2019).
- Analysis of osteoporosis diagnosis and statin prescription data.
- Joinpoint regression for trend analysis (APC, AAPC) stratified by age and gender.
Main Results:
- Overall statin prescription prevalence (AAPC: -1.03%) and incidence (AAPC: -1.82%) significantly decreased.
- Male patients showed higher rates and steeper declines, leading to convergence with females.
- Age-specific analysis revealed steepest declines in the 70-79 group; a 2018 breakpoint suggested guideline influence.
Conclusions:
- Declining statin use in osteoporosis patients, particularly males, suggests evolving risk-benefit assessments.
- High discontinuation rates point to challenges in long-term cardiovascular protection.
- Need for updated guidelines addressing statin initiation and adherence in multimorbid patients.
Abstract:
Statin prescribing patterns in osteoporosis patients remain uncharacterized despite cardiovascular disease being a leading cause of mortality in this population. This study examined temporal trends and demographic variations in statin prescription rates among osteoporosis patients in the UK. This research is a retrospective cohort study utilizing the IQVIA Medical Research Data (IMRD) spanning 2005-2019. Patients' diagnosis of osteoporosis and corresponding statin prescription data were extracted. Prevalence and incidence of statin prescription were calculated, followed by age-stratified and gender-stratified trends analysis using joinpoint regression to calculate the average percent change (APC), annual average percent change (AAPC), and identify significant temporal shifts. Among 157,483 identified osteoporosis patients, statin prescribing trends demonstrated significant reductions in both prescription prevalence (AAPC: -1.03%, p = 0.005) and incidence rate (AAPC:-1.82%, p < 0.001). Gender-based analysis revealed higher prescription rates and more pronounced declines in male patients (prevalence AAPC:2.7% vs female -0.8%), resulting in prescription rate convergence by study end. Age stratified findings showed the 70-79 years age group maintained the highest initial prevalence but experienced the steepest declines. A notable breakpoint occurred in 2018 within the 50-59 age cohort, which may be a result of stricter ACC/AHA cholesterol guidelines requiring enhanced risk-based criteria for primary and secondary prevention. The prescription peaks in 2006 and 2014 likely coincided with NICE guideline modifications. Despite these guideline expansions encouraging broader statin use, sensitivity analysis of cumulative defined daily dose revealed persistently high discontinuation rates in osteoporosis patients. These patterns indicate substantial gaps in cardiovascular protection for this vulnerable population. Declining statin prescription trends among osteoporosis patients, particularly among elderly males, appear to reflect an evolution in clinical practices toward risk-benefit assessment. These findings highlight the need for treatment guideline advancement that addresses both appropriate statin initiation and strategies to improve long-term adherence in patients with multimorbidity.
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