Li Ming, McDermott Robyn
Centre of Population Health Research, University of South Australia, IPC CWE-48, GPO Box 2471, Adelaide, SA, Australia 5001.
Centre of Population Health Research, University of South Australia, IPC CWE-48, GPO Box 2471, Adelaide, SA, Australia 5001; Faculty of Medicine, Health & Molecular Sciences, James Cook University, Cairns, Australia 4870;.
J Diabetes Complications. 2017 Apr;31(4):708-714. doi: 10.1016/j.jdiacomp.2016.12.008. Epub 2017 Jan 5.
To document risk factors of all-cause mortality in a cohort of indigenous Australians from 23 communities of North Queensland during 1998-2006.
Among 2787 indigenous adults, baseline weight, waist circumference, blood pressure, fasting glucose, lipids, gamma-glutamyl transferase, urine albumin creatinine ratio, smoking, alcohol intake and physical activity were measured in 1998-2000. Deaths were ascertained from State Registry of Deaths, hospitalization and clinical records till 2006. Mortality risk factors were assessed using a Cox proportional-hazards model.
The standardized all-cause mortality rate was 23.2/1000 person-years (95% CI 20.3-26.3/1000 pys). After adjusting for age, sex, and ethnicity, baseline plasm fasting glucose >=5.5mmol/L was associated with a 50% increased risk of death (HR 1.5, 95% CI 1.2-2.0). Albuminuria was associated with all-cause mortality with a hazards ratio of 1.4 for microalbuminuria (95% CI 1.0-1.9) and 2.6 (95% CI 1.8-3.7) for macroalbuminuria. Gamma-glutamyl transferase >=50IU was associated with an increased risk of all-cause mortality by 40% (95% CI 1.04-1.8).
Fasting glycaemia, albuminuria, and gamma-glutamyl transferase, may be a marker for all-cause mortality within this cohort.
记录1998 - 2006年期间北昆士兰23个社区的澳大利亚原住民队列中全因死亡率的风险因素。
在2787名原住民成年人中,于1998 - 2000年测量了基线体重、腰围、血压、空腹血糖、血脂、γ-谷氨酰转移酶、尿白蛋白肌酐比值、吸烟、酒精摄入量和身体活动情况。通过州死亡登记处、住院记录和临床记录确定直至2006年的死亡情况。使用Cox比例风险模型评估死亡率风险因素。
标准化全因死亡率为23.2/1000人年(95%可信区间20.3 - 26.3/1000人年)。在调整年龄、性别和种族后,基线血浆空腹血糖≥5.5mmol/L与死亡风险增加50%相关(风险比1.5,95%可信区间1.2 - 2.0)。蛋白尿与全因死亡率相关,微量蛋白尿的风险比为1.4(95%可信区间1.0 - 1.9),大量蛋白尿的风险比为2.6(95%可信区间1.8 - 3.7)。γ-谷氨酰转移酶≥50IU与全因死亡率风险增加40%相关(95%可信区间1.04 - 1.8)。
空腹血糖、蛋白尿和γ-谷氨酰转移酶可能是该队列中全因死亡率的一个标志物。