英国生物数据库中 APOE E4 等位基因与青光眼诊断年龄之间的女性特异性关联。

Q2 Medicine Ophthalmology. Glaucoma Pub Date : 2024-08-07 DOI:10.1016/j.ogla.2024.07.009
Yan Shi, Junming Hu, William Liu, Wei Qiao Qiu, Xinyue He, Miao Zhang, Yan Gao, Xiaoling Zhang, Zhigang Fan
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引用次数: 0

摘要

目的通过说明包括载脂蛋白E(APOE)E4等位基因、性别和眼压(IOP)在内的风险因素对青光眼诊断年龄(AAD)的相互作用,探讨载脂蛋白E(APOE)E4等位基因在青光眼性别特异性衰老过程中的影响:一项横断面研究纳入了英国生物数据库中具有完整数据(2006-2010 年)的参与者进行分析。参与者:2236 名青光眼患者和 103232 名对照者:我们使用线性混合模型(LMM)分析评估了青光眼AAD、APOE E4等位基因(0:不存在;1:存在)与眼压之间的多变量调整关系,并按AAD的平均绝经年龄(50岁)和性别对各组进行了分层:主要结果测量指标:青光眼的 AAD、APOE E4 等位基因和眼压:结果:与对照组相比,青光眼患者年龄较大,男性比例较高,平均眼压较高(均为 P <0.001)。将青光眼患者按年龄 50 岁和性别进一步分层,在单变量 LMM 中,年龄小于 50 岁的女性中,较低的眼压(根据年龄调整的模型 1,βIOP=-0.096±0.041,P=0.019)和阳性 APOE E4 等位基因(根据年龄和眼压调整的模型 2,βe4=1.093±0.488,P=0.026)与年龄较大的年龄相关。在按年龄调整的多变量 LMM 中(模型 3),随着贝塔值的增加,这两个因素在多变量模型中的效应大小也随之增加。(βIOP=-0.111±0.040,P=0.007;βe4=1.235±0.485,P=0.012)(模型 1 vs 模型 3:P=0.011)。在AAD≥50岁的女性中,只有APOE E4等位基因阳性(经年龄和眼压调整,βe4=-1.121±0.412,P=0.007)与更年轻的AAD相关。结论:APOE E4等位基因可能与年龄和眼压有关(βe4=-1.121±0.412,P=0.007):APOE E4等位基因可能会在女性更年期的平均年龄50岁左右的过渡时期延迟青光眼的发展,随后加速其发展,重要的是,这与眼压无关。了解每个年龄阶段的具体过渡状态和可改变的因素,对于制定促进健康老龄化的干预措施或策略至关重要。
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Female-Specific Association between the Apolipoprotein E E4 Allele and Age at Diagnosis of Glaucoma in UK Biobank.

Objective: To explore the impact of the apolipoprotein E (APOE) E4 allele in the gender-specific aging process in glaucoma by illustrating the interaction between risk factors, including the APOE E4 allele, gender, and intraocular pressure (IOP), for age at diagnosis (AAD) of glaucoma.

Design: A cross-sectional study included UK Biobank participants with complete data (2006-2010) for analysis. Data were analyzed in December 2023.

Participants: Two thousand two hundred thirty-six glaucoma patients and 103 232 controls.

Methods: We evaluated multivariable-adjusted associations of AAD of glaucoma, APOE E4 allele (0: absence; 1: presence), and IOP using linear mixed model (LMM) analyses across groups stratified by AAD of mean age of menopause (50 years) and gender.

Main outcomes measures: Age at diagnosis of glaucoma, APOE E4 allele, and IOP.

Results: Patients with glaucoma were older and had a higher percentage of males and a higher mean IOP compared to controls (all P < 0.001). Further stratifying the patients with glaucoma by AAD of 50 and gender, lower IOP (model 1 adjusted by age, βIOP = -0.096 ± 0.041, P = 0.019), and positive APOE E4 allele (model 2 adjusted by age and IOP, βe4 = 1.093 ± 0.488, P = 0.026) were associated with an older AAD in females with an AAD <50 years under univariate LMM. In multivariate LMM adjusted by age (model 3), the effect size of both factors increased in the multivariate model as the beta-value increased (βIOP = -0.111 ± 0.040, P = 0.007; βe4 = 1.235 ± 0.485, P = 0.012) (model 1 vs. model 3: P = 0.011). In females with an AAD ≥50 years, only positive APOE E4 allele (adjusted by age and IOP, βe4 = -1.121 ± 0.412, P = 0.007) was associated with a younger AAD. In males, only higher IOP was associated with an older AAD in those with an AAD ≥50 years (βIOP = 0.088 ± 0.032, P = 0.006).

Conclusions: Apolipoprotein E E4 allele may initially delay and later accelerate the development of glaucoma in females around the transition period of 50 years, which is the mean age of menopause, and importantly, this is independent of IOP. Understanding the specific transition states and modifiable factors within each age phase is crucial for developing interventions or strategies that promote healthy aging.

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

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来源期刊
Ophthalmology. Glaucoma
Ophthalmology. Glaucoma Medicine-Medicine (all)
CiteScore
4.20
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0.00%
发文量
140
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