Department of Clinical and Experimental Medicine, School of Biosciences and Medicine, University of Surrey, Guildford GU2 7XH, UK.
Department of Clinical and Experimental Medicine, School of Biosciences and Medicine, University of Surrey, Guildford GU2 7XH, UK; Nuffield Department of Primary Care Health Sciences, Radcliffe Primary Care Building, Radcliffe Observatory Quarter, Woodstock Road, University of Oxford, Oxford OX2 6GG, UK.
Diabetes Res Clin Pract. 2021 May;175:108776. doi: 10.1016/j.diabres.2021.108776. Epub 2021 Mar 19.
To determine, inreal-world primary care settings, the prevalence of, and risk factors for, retinopathy atType 2 diabetes mellitus diagnosis and report cumulative incidence and progression of retinopathy seven years after diabetes diagnosis.
Retrospective cohort analysis of people with newly diagnosed Type 2 diabetesrecorded bythe Royal College of General Practitioners Research and Surveillance Centre(between 2005 and 2009, n=11,399).Outcomes included; retinopathy prevalence atdiabetesdiagnosis (baseline) and cumulative incidence or progression of retinopathy at seven years. Retinopathy prevalence was compared with the United Kingdom Prospective Diabetes Study (UKPDS-1998). Factors influencing retinopathy incidence and progression were analysed using logistic regression.
Baseline retinopathy prevalencewas 18% (n=2,048) versus 37% in UKPDS. At seven years, 11.6% (n=237) of those with baseline retinopathyhad progression of retinopathy. In those without baseline retinopathy, 46.4% (n=4,337/9,351) developed retinopathy by seven years. Retinopathy development (OR: 1.05 [95%CI: 1.02-1.07] per mmol/mol increase) and progression (OR: 1.05 [1.04-1.06]) at seven years was associated with higher HbAatdiabetesdiagnosis. Obesity (OR: 0.88 [0.79-0.98]) and high socioeconomic status (OR: 0.63 [0.53-0.74]) were negatively associated with retinopathy development at seven years.
Baseline retinopathy prevalence has declined since UKPDS. Additionally, HbA at diabetes diagnosis remains important for retinopathy development and progression.
在真实的初级保健环境中,确定 2 型糖尿病诊断时视网膜病变的患病率和危险因素,并报告糖尿病诊断后 7 年视网膜病变的累积发生率和进展情况。
对皇家全科医师学院研究和监测中心(2005 年至 2009 年间)记录的新诊断为 2 型糖尿病的患者进行回顾性队列分析(n=11399)。结局包括:糖尿病诊断时(基线)视网膜病变的患病率以及 7 年后视网膜病变的累积发生率或进展。将视网膜病变的患病率与英国前瞻性糖尿病研究(UKPDS-1998)进行比较。使用逻辑回归分析影响视网膜病变发生率和进展的因素。
基线时视网膜病变的患病率为 18%(n=2048),而 UKPDS 为 37%。在 7 年内,基线时有视网膜病变的患者中有 11.6%(n=237)出现视网膜病变进展。在基线时无视网膜病变的患者中,有 46.4%(n=4337/9351)在 7 年内发生了视网膜病变。7 年内视网膜病变的发生(OR:1.05[95%CI:1.02-1.07]每 mmol/mol 增加)和进展(OR:1.05[1.04-1.06])与糖尿病诊断时 HbA1c 升高有关。肥胖(OR:0.88[0.79-0.98])和高社会经济地位(OR:0.63[0.53-0.74])与 7 年内视网膜病变的发生呈负相关。
自 UKPDS 以来,基线时视网膜病变的患病率有所下降。此外,糖尿病诊断时的 HbA1c 仍然是视网膜病变发生和进展的重要因素。