دورية أكاديمية

Angiotensin‐converting enzyme inhibitors and risk of age‐related macular degeneration in individuals with hypertension.

التفاصيل البيبلوغرافية
العنوان: Angiotensin‐converting enzyme inhibitors and risk of age‐related macular degeneration in individuals with hypertension.
المؤلفون: Subramanian, Anuradhaa, Han, Diana, Braithwaite, Tasanee, Thayakaran, Rasiah, Zemedikun, Dawit T., Gokhale, Krishna M., Lee, Wen Hwa, Coker, Jesse, Keane, Pearse A., Denniston, Alastair K., Nirantharakumar, Krishnarajah, Azoulay, Laurent, Adderley, Nicola J.
المصدر: British Journal of Clinical Pharmacology; Sep2022, Vol. 88 Issue 9, p4199-4210, 12p
مصطلحات موضوعية: MACULAR degeneration, ENZYME inhibitors, ACE inhibitors, ANGIOTENSIN-receptor blockers, CALCIUM antagonists, PROPORTIONAL hazards models, PROPENSITY score matching, HYPERTENSION
مصطلحات جغرافية: UNITED Kingdom
مستخلص: Aims: Several observational studies have examined the potential protective effect of angiotensin‐converting enzyme inhibitor (ACE‐I) use on the risk of age‐related macular degeneration (AMD) and have reported contradictory results owing to confounding and time‐related biases. We aimed to assess the risk of AMD in a base cohort of patients aged 40 years and above with hypertension among new users of ACE‐I compared to an active comparator cohort of new users of calcium channel blockers (CCB) using data obtained from IQVIA Medical Research Data, a primary care database in the UK. Methods: In this study, 53 832 and 43 106 new users of ACE‐I and CCB were included between 1995 and 2019, respectively. In an on‐treatment analysis, patients were followed up from the time of index drug initiation to the date of AMD diagnosis, loss to follow‐up, discontinuation or switch to the comparator drug. A comprehensive range of covariates were used to estimate propensity scores to weight and match new users of ACE‐I and CCB. Standardized mortality ratio weighted Cox proportional hazards model was used to estimate hazard ratios of developing AMD. Results: During a median follow‐up of 2 years (interquartile range 1–5 years), the incidence rate of AMD was 2.4 (95% confidence interval 2.2–2.6) and 2.2 (2.0–2.4) per 1000 person‐years among the weighted new users of ACE‐I and CCB, respectively. There was no association of ACE‐I use on the risk of AMD compared to CCB use in either the propensity score weighted or matched, on‐treatment analysis (adjusted hazard ratio: 1.07 [95% confidence interval 0.90–1.27] and 0.87 [0.71–1.07], respectively). Conclusion: We found no evidence that the use of ACE‐I is associated with risk of AMD in patients with hypertension. [ABSTRACT FROM AUTHOR]
Copyright of British Journal of Clinical Pharmacology is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
قاعدة البيانات: Complementary Index
الوصف
تدمد:03065251
DOI:10.1111/bcp.15366