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年龄相关性黄斑变性与胆石症的关联

Association of Age-Related Macular Degeneration with Cholelithiasis.

作者信息

Zhang Kevin R, Nair Rohini M, Chen Yineng, Jin Fangming, Dunaief Joshua, VanderBeek Brian L

机构信息

Department of Ophthalmology, Scheie Eye Institute, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania.

Center for Preventative Ophthalmology and Biostatistics, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania.

出版信息

Ophthalmol Sci. 2025 Mar 19;5(4):100771. doi: 10.1016/j.xops.2025.100771. eCollection 2025 Jul-Aug.

Abstract

PURPOSE

Dysregulated lipid metabolism likely contributes to the pathogenesis of age-related macular degeneration (AMD). There is an overlap in risk factors between AMD and diseases of lipid metabolism, such as cholelithiasis, suggesting that an association between these diseases could provide insight into AMD pathogenesis. This study sought to determine if there is an association between cholelithiasis and AMD.

DESIGN

A cohort study was conducted using patients in the Optum deidentified Clinformatics Data Mart database from January 1, 2000, to June 30, 2022.

PARTICIPANTS

Patients over the age of 55 with ≥2 years of data and no prior history of AMD were included. The exposed cohort included patients who had a history of cholelithiasis, cholecystitis, or cholecystectomy. The control cohort included patients with gastroesophageal reflux disease (GERD), matched for age ±3 years, sex, race, and year of index date.

METHODS

Propensity scores were created using multivariable logistic regression and applied to inverse probability of treatment weighting (IPTW). Cox proportional hazard regression modeling with IPTW was used to compare progression to AMD in each cohort.

MAIN OUTCOME MEASURES

Progression to AMD for patients with cholelithiasis, cholecystitis, or a history of cholecystectomy.

RESULTS

A total of 332 536 patients with cholelithiasis and 776 591 matched GERD controls were analyzed. After IPTW, the mean age (±standard deviation) was 66.6 ± 9.4 years in the cholelithiasis cohort and 67.5 (±10.3) years in the GERD cohort. Women comprised 58% of the cholelithiasis cohort and 57% of the GERD cohort. In the cholelithiasis cohort, 3511.7 (1.14%) were diagnosed with AMD, compared with 23 367.1 (2.92%) in the GERD cohort and corresponding to a significantly decreased hazard of AMD (adjusted hazard ratio [aHR] = 0.72, 95% confidence interval [CI]: 0.69-0.75,  < 0.0001). In the subanalysis, before IPTW weighting, AMD developed in 3809 of 275 897 (1.4%) patients with only cholelithiasis (aHR = 0.76, 95% CI: 0.73-0.80,  < 0.0001), 335 of 47 166 (0.71%) patients with cholecystitis (aHR = 0.54, 95% CI: 0.47-0.61,  < 0.0001), and 114 of 9473 (1.20%) patients who underwent cholecystectomy (aHR = 0.50, 95% CI: 0.41-0.63,  < 0.0001).

CONCLUSIONS

Cholelithiasis was associated with a 28% hazard reduction in AMD. More severe gallbladder disease conferred greater protection.

FINANCIAL DISCLOSURES

Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.

摘要

目的

脂质代谢失调可能在年龄相关性黄斑变性(AMD)的发病机制中起作用。AMD与脂质代谢疾病(如胆石症)的危险因素存在重叠,这表明这些疾病之间的关联可能有助于深入了解AMD的发病机制。本研究旨在确定胆石症与AMD之间是否存在关联。

设计

使用Optum去识别化临床信息数据集市数据库中2000年1月1日至2022年6月30日的患者进行队列研究。

参与者

纳入年龄在55岁以上、有≥2年数据且无AMD既往史的患者。暴露队列包括有胆石症、胆囊炎或胆囊切除术病史的患者。对照队列包括年龄相差±3岁、性别、种族和索引日期年份相匹配的胃食管反流病(GERD)患者。

方法

使用多变量逻辑回归创建倾向评分,并应用于治疗加权逆概率(IPTW)。采用带有IPTW的Cox比例风险回归模型比较各队列中进展为AMD的情况。

主要观察指标

有胆石症、胆囊炎或胆囊切除术病史的患者进展为AMD的情况。

结果

共分析了332536例胆石症患者和776591例匹配的GERD对照。经过IPTW后,胆石症队列的平均年龄(±标准差)为66.6±9.4岁,GERD队列的平均年龄为67.5(±10.3)岁。女性在胆石症队列中占58%,在GERD队列中占57%。在胆石症队列中,3511.7例(1.14%)被诊断为AMD,而GERD队列中有23367.1例(2.92%),这对应着AMD风险显著降低(调整后风险比[aHR]=0.72,95%置信区间[CI]:0.69 - 0.75,P<0.0001)。在亚分析中,在IPTW加权之前,仅患有胆石症的275897例患者中有3809例(1.4%)发生AMD(aHR = 0.76,95% CI:0.73 - 0.80,P<0.0001),患有胆囊炎的47166例患者中有335例(0.71%)(aHR = 0.54,95% CI:0.47 - 0.61,P<0.0001),接受胆囊切除术的9473例患者中有114例(1.20%)(aHR = 0.50,95% CI:0.41 - 0.63,P < 0.0001)。

结论

胆石症与AMD风险降低28%相关。更严重的胆囊疾病提供了更大的保护作用。

财务披露

在本文末尾的脚注和披露中可能会发现专有或商业披露信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2f2/12022688/78c19fd6d3b8/gr1.jpg

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