Albumin-Corrected Fructosamine Predicts All-Cause and Non-CVD Mortality Among the Very Elderly Aged 80 Years or Older Without Diabetes

Author:

Zhou Jinhui1,Lv Yuebin1,Zhao Feng1,Wei Yuan12,Gao Xiang3ORCID,Chen Chen1ORCID,Lu Feng1,Liu Yingchun1,Li Chengcheng1,Wang Jiaonan14,Zhang Xiaochang5,Gu Heng1,Yin Zhaoxue5,Cao Zhaojin1,Kraus Virginia B6,Mao Chen7,Shi Xiaoming14

Affiliation:

1. China CDC Key Laboratory of Environment and Population Health, National Institute of Environmental Health, Chinese Center for Disease Control and Prevention, Beijing, China

2. Department of Epidemiology and Biostatistics, School of Public Health, Jilin University, Changchun, China

3. Department of Nutritional Sciences, The Pennsylvania State University, University Park, Pennsylvania, USA

4. Center for Global Health, School of Public Health, Nanjing Medical University, Nanjing, China

5. Division of Non-communicable Disease and Healthy Ageing Management, Chinese Center for Disease Control and Prevention, Beijing, China

6. Duke Molecular Physiology Institute and Division of Rheumatology, Department of Medicine, Duke University School of Medicine, Durham, North Carolina, USA

7. Division of Epidemiology, School of Public Health, Southern Medical University, Guangzhou, China

Abstract

Abstract Background Several guidelines have suggested alternative glycemic markers for hemoglobin A1c among older adults with limited life expectancy or multiple coexisting chronic illnesses. We evaluated associations between fructosamine, albumin-corrected fructosamine (AlbF), fasting plasma glucose (FPG), and mortality in the diabetic and nondiabetic subpopulations, and compared which marker better predicts mortality among participants aged 80 and older. Methods Included were 2 238 subjects from the Healthy Ageing and Biomarkers Cohort Study (2012–2018) and 207 participants had diabetes at baseline. Multivariable Cox proportional hazards regression models investigated the associations of fructosamine, AlbF, FPG, and all-cause, cardiovascular disease (CVD), and non-CVD mortality in the diabetic and nondiabetic subpopulations. Restricted cubic splines explored potential nonlinear relations. C-statistic, integrated discrimination improvement (IDI), and net reclassification improvement (NRI) evaluated the additive value of different glycemic markers to predict mortality. Results Overall, 1 191 deaths were documented during 6 793 person-years of follow-up. In the linear model, per unit increases of fructosamine, AlbF, and FPG were associated with a higher risk of mortality in nondiabetic participants, with hazard ratios of 1.02 (1.00, 1.05), 1.27 (1.14, 1.42), and 1.04 (0.98, 1.11) for all-cause mortality, and 1.04 (1.00, 1.07), 1.38 (1.19, 1.59), and 1.10 (1.01, 1.19) for non-CVD mortality, respectively. Comparisons indicated that AlbF better predicts all-cause and non-CVD mortality in nondiabetic participants with significant improvement in IDI and NRI. Conclusions Higher concentrations of fructosamine, AlbF, and FPG were associated with a higher risk of all-cause or non-CVD mortality among the very elderly where AlbF may constitute an alternative prospective glycemic predictor of mortality.

Funder

National Natural Science Foundation of China

National Institute on Aging

Claude D. Pepper Older Americans Independence Centers

Publisher

Oxford University Press (OUP)

Subject

Geriatrics and Gerontology,Aging

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