Lehrer Steven, Rheinstein Peter H
Department of Radiation Oncology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Severn Health Solutions, Severna Park, MD, USA.
Clin Hypertens. 2024 Nov 1;30(1):33. doi: 10.1186/s40885-024-00290-9.
The use of calcium channel blockers is associated with primary open-angle glaucoma (POAG) in a statistically meaningful but minor way. In general, those who had received calcium channel blocker medication were at a 23% increased risk of developing glaucoma in comparison to those who had never taken the antihypertensive drugs. We wished to confirm this association and examine POAG genes that might be involved, since the genetics has not yet been analyzed.
We used MedWatch and UK Biobank data to evaluate the effects of amlodipine on POAG and intraocular pressure (IOP). We analyzed three POAG-associated single-nucleotide polymorphisms: rs9913911, an intron variant in growth arrest-specific 7 (GAS7), one of the genes that influences IOP; rs944801, an intron variant within CDKN2B-AS1, and rs2093210, an intron variant within SIX6, known to be associated with vertical cup-disc ratio, an important optic nerve head parameter that is often used to define or diagnose glaucoma.
Amlodipine use in MedWatch doubled the prevalence of POAG, from 0.0805 to 0.177%, a small but significant increase. Multivariate analysis by logistic regression of UK Biobank data revealed that POAG risk was significantly increased with age, male sex, major alleles of rs9913911 (GAS7) and rs944801 (CDKN2B-AS1), and minor allele of rs2093210 (SIX6). Amlodipine increased POAG risk by 16.1% (P = 0.032). Amlodipine has not been associated with increased IOP. We confirmed this lack of association and in addition found that GAS7, associated with IOP, was not associated with POAG risk and amlodipine. But CDKN2B-AS1 and SIX6, POAG genes not associated with IOP, were associated with POAG and amlodipine.
Amlodipine, a frequently prescribed drug and first line treatment for hypertension, has a potentially hazardous relationship with POAG. Knowledge of this link can guide the prescribing of alternate drugs for hypertensive individuals who have glaucoma or are at risk for it. Diuretics and β-blockers are not associated with POAG or increased IOP and could be substituted for amlodipine in hypertensive patients at risk POAG.
None.
钙通道阻滞剂的使用与原发性开角型青光眼(POAG)存在统计学意义上的关联,但关联程度较小。一般来说,与从未服用过抗高血压药物的人相比,服用过钙通道阻滞剂药物的人患青光眼的风险增加了23%。由于尚未对遗传学进行分析,我们希望证实这种关联并研究可能涉及的POAG相关基因。
我们使用MedWatch和英国生物银行的数据来评估氨氯地平对POAG和眼压(IOP)的影响。我们分析了三个与POAG相关的单核苷酸多态性:rs9913911,生长停滞特异性7(GAS7)基因的内含子变异,该基因是影响眼压的基因之一;rs944801,CDKN2B-AS1基因内的内含子变异,以及rs2093210,SIX6基因内的内含子变异,已知其与垂直杯盘比相关,垂直杯盘比是一个重要的视神经乳头参数,常用于定义或诊断青光眼。
在MedWatch中,使用氨氯地平使POAG的患病率翻倍,从0.0805%增至0.177%,虽增幅较小但具有统计学意义。对英国生物银行数据进行逻辑回归的多变量分析显示,POAG风险随年龄、男性性别、rs9913911(GAS7)和rs944801(CDKN2B-AS1)的主要等位基因以及rs2093210(SIX6)的次要等位基因显著增加。氨氯地平使POAG风险增加了16.1%(P = 0.032)。氨氯地平与眼压升高无关。我们证实了这种缺乏关联的情况,此外还发现,与眼压相关的GAS7与POAG风险及氨氯地平无关。但与眼压无关的POAG相关基因CDKN2B-AS1和SIX6与POAG及氨氯地平有关。
氨氯地平是一种常用的高血压处方药和一线治疗药物,与POAG存在潜在的有害关系。了解这种关联可为患有青光眼或有青光眼风险的高血压患者选择替代药物提供指导。利尿剂和β受体阻滞剂与POAG或眼压升高无关,可替代氨氯地平用于有POAG风险的高血压患者。
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