Newman-Casey Paula Anne, Stem Maxwell, Talwar Nidhi, Musch David C, Besirli Cagri G, Stein Joshua D
Department of Ophthalmology and Visual Sciences, University of Michigan Medical School, Ann Arbor, Michigan.
Department of Ophthalmology and Visual Sciences, University of Michigan Medical School, Ann Arbor, Michigan.
Ophthalmology. 2014 Oct;121(10):1939-48. doi: 10.1016/j.ophtha.2014.04.045. Epub 2014 Jun 20.
To determine risk factors associated with development of a branch retinal vein occlusion (BRVO) among a large group of managed-care plan beneficiaries in the United States.
Retrospective, longitudinal cohort study.
All beneficiaries age ≥55 years continuously enrolled for ≥2 years in a managed care network from 2001-2009 who had ≥2 visits to an eye care provider.
Multivariable Cox regression analyses identified sociodemographic factors, ocular and nonocular conditions associated with incident BRVO.
Hazard of incident BRVO with 95% confidence interval (CI).
Of the 492,488 enrollees who met inclusion criteria, 2283 (0.5%) developed incident BRVO. After adjustment for confounding factors, blacks (adjusted hazard ratio [aHR], 1.43; CI, 1.19-1.73; P = 0.0001) had a 43% increased hazard of BRVO relative to non-Hispanic whites. Enrollees with hypertension (HTN) alone (aHR, 1.78; CI, 1.36-2.32; P < 0.0001) or HTN along with other metabolic syndrome components (diabetes mellitus [DM] and hyperlipidemia; aHR, 1.44; CI, 1.12-1.84; P = 0.005) had an increased hazard of developing a BRVO compared with those with none of these conditions. Disease severity was important; enrollees with end-organ damage caused by HTN had a 107% increased hazard of developing BRVO compared with enrollees without HTN (aHR, 2.07; CI, 1.75-2.45; P < 0.0001). Although there was no association between DM without end-organ damage and BRVO (aHR, 0.92; CI, 0.81-1.04; P = 0.2), individuals with end-organ damage from DM had a 36% increased hazard of BRVO (aHR, 1.36; CI, 1.18-1.57; P < 0.0001) compared with those without DM. Although cerebrovascular accident was associated with an increased hazard of developing BRVO (aHR, 1.34; CI, 1.19-1.52; P < 0.0001), other diseases of the vascular system (deep venous thrombosis/pulmonary embolism, peripheral vascular disease, hypercoagulable state, myocardial infarction) or anticoagulant use did not increase the risk of BRVO (P > 0.10 for all comparisons).
Both HTN and end-organ damage from DM contribute to arteriosclerosis, atherosclerosis, and endothelial dysfunction, which seem to be major risk factors for BRVO. Ophthalmologists should emphasize to patients and their primary physicians the importance of effectively managing systemic medical conditions associated with BRVO.
确定美国一大群管理式医疗计划受益人群中与视网膜分支静脉阻塞(BRVO)发生相关的危险因素。
回顾性纵向队列研究。
2001年至2009年期间在管理式医疗网络中连续登记≥2年且年龄≥55岁、并至少有2次眼科就诊记录的所有受益人。
多变量Cox回归分析确定与BRVO发病相关的社会人口学因素、眼部和非眼部疾病。
BRVO发病风险及95%置信区间(CI)。
在符合纳入标准的492488名登记者中,2283人(0.5%)发生了BRVO。在对混杂因素进行调整后,黑人(调整后风险比[aHR]为1.43;CI为1.19 - 1.73;P = 0.0001)发生BRVO的风险相对于非西班牙裔白人增加了43%。仅患有高血压(HTN)的登记者(aHR为1.78;CI为1.36 - 2.32;P < 0.0001)或患有高血压以及其他代谢综合征成分(糖尿病[DM]和高脂血症;aHR为1.44;CI为1.12 - 1.84;P = 0.005)的登记者发生BRVO的风险高于无这些疾病的登记者。疾病严重程度很重要;因高血压导致终末器官损害的登记者发生BRVO的风险比无高血压的登记者增加了107%(aHR为2.07;CI为1.75 - 2.45;P < 0.0001)。虽然无终末器官损害的糖尿病与BRVO之间无关联(aHR为0.92;CI为0.81 - 1.04;P = 0.2),但因糖尿病导致终末器官损害的个体发生BRVO的风险比无糖尿病的个体增加了36%(aHR为1.36;CI为1.18 - 1.57;P < 0.0001)。虽然脑血管意外与发生BRVO的风险增加相关(aHR为1.34;CI为1.19 - 1.52;P < 0.0001),但其他血管系统疾病(深静脉血栓形成/肺栓塞、外周血管疾病、高凝状态、心肌梗死)或使用抗凝剂并未增加BRVO的风险(所有比较的P > 0.10)。
高血压和糖尿病导致的终末器官损害均会导致动脉硬化、动脉粥样硬化和内皮功能障碍,这似乎是BRVO的主要危险因素。眼科医生应向患者及其初级医生强调有效控制与BRVO相关的全身性疾病的重要性。