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Serum lutein is a promising biomarker for type 2 diabetes mellitus and diabetic kidney disease in the elderly

OBJECTIVE: To investigate the relationship between serum lutein and type 2 diabetes mellitus (T2DM) and diabetic kidney disease (DKD) in elderly individuals. METHODS: A total of 60 T2DM patients over 60 years were subgrouped into a DKD group and a non‐DKD group according to their urinary microalbumi...

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Autores principales: Pan, Fenghui, Cui, Wenxia, Gao, Lei, Shi, Xiaoting, Yang, Haiyan, Hu, Yun, Li, Man
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8993643/
https://www.ncbi.nlm.nih.gov/pubmed/35293029
http://dx.doi.org/10.1002/jcla.24350
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author Pan, Fenghui
Cui, Wenxia
Gao, Lei
Shi, Xiaoting
Yang, Haiyan
Hu, Yun
Li, Man
author_facet Pan, Fenghui
Cui, Wenxia
Gao, Lei
Shi, Xiaoting
Yang, Haiyan
Hu, Yun
Li, Man
author_sort Pan, Fenghui
collection PubMed
description OBJECTIVE: To investigate the relationship between serum lutein and type 2 diabetes mellitus (T2DM) and diabetic kidney disease (DKD) in elderly individuals. METHODS: A total of 60 T2DM patients over 60 years were subgrouped into a DKD group and a non‐DKD group according to their urinary microalbumin‐to‐creatinine ratio (UACR), while 30 age‐matched non‐T2DM patients were recruited in the control group. Baseline characteristics, laboratory examination results, and serum lutein levels were compared, and their correlations were analyzed. Receiver operating characteristic (ROC) curves were plotted to identify the diagnostic potential of lutein in T2DM and DKD. RESULTS: The lutein level in the T2DM group was significantly lower than that in the control group and was also significantly lower in the DKD group than in the non‐DKD group (p < 0.001). Lutein levels were negatively correlated with body mass index, glycosylated hemoglobin, fasting blood glucose, triglyceride, and UACR and positively correlated with high‐density lipoprotein cholesterol (p < 0.05). T2DM patients were divided into four groups according to the quartile of their lutein level. The proportion of T2DM and DKD gradually decreased with increasing lutein levels (p < 0.001). The area under the ROC curve of serum lutein in diagnosing T2DM and DKD was 0.880 and 0.779, respectively, with corresponding cut‐off values of 0.433 μmol/L and 0.197 μmol/L (p < 0.001). CONCLUSION: The serum level of lutein is negatively correlated with the incidence of T2DM and DKD in the elderly and can serve as a diagnostic marker for T2DM and DKD.
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spelling pubmed-89936432022-04-13 Serum lutein is a promising biomarker for type 2 diabetes mellitus and diabetic kidney disease in the elderly Pan, Fenghui Cui, Wenxia Gao, Lei Shi, Xiaoting Yang, Haiyan Hu, Yun Li, Man J Clin Lab Anal Research Articles OBJECTIVE: To investigate the relationship between serum lutein and type 2 diabetes mellitus (T2DM) and diabetic kidney disease (DKD) in elderly individuals. METHODS: A total of 60 T2DM patients over 60 years were subgrouped into a DKD group and a non‐DKD group according to their urinary microalbumin‐to‐creatinine ratio (UACR), while 30 age‐matched non‐T2DM patients were recruited in the control group. Baseline characteristics, laboratory examination results, and serum lutein levels were compared, and their correlations were analyzed. Receiver operating characteristic (ROC) curves were plotted to identify the diagnostic potential of lutein in T2DM and DKD. RESULTS: The lutein level in the T2DM group was significantly lower than that in the control group and was also significantly lower in the DKD group than in the non‐DKD group (p < 0.001). Lutein levels were negatively correlated with body mass index, glycosylated hemoglobin, fasting blood glucose, triglyceride, and UACR and positively correlated with high‐density lipoprotein cholesterol (p < 0.05). T2DM patients were divided into four groups according to the quartile of their lutein level. The proportion of T2DM and DKD gradually decreased with increasing lutein levels (p < 0.001). The area under the ROC curve of serum lutein in diagnosing T2DM and DKD was 0.880 and 0.779, respectively, with corresponding cut‐off values of 0.433 μmol/L and 0.197 μmol/L (p < 0.001). CONCLUSION: The serum level of lutein is negatively correlated with the incidence of T2DM and DKD in the elderly and can serve as a diagnostic marker for T2DM and DKD. John Wiley and Sons Inc. 2022-03-15 /pmc/articles/PMC8993643/ /pubmed/35293029 http://dx.doi.org/10.1002/jcla.24350 Text en © 2022 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Pan, Fenghui
Cui, Wenxia
Gao, Lei
Shi, Xiaoting
Yang, Haiyan
Hu, Yun
Li, Man
Serum lutein is a promising biomarker for type 2 diabetes mellitus and diabetic kidney disease in the elderly
title Serum lutein is a promising biomarker for type 2 diabetes mellitus and diabetic kidney disease in the elderly
title_full Serum lutein is a promising biomarker for type 2 diabetes mellitus and diabetic kidney disease in the elderly
title_fullStr Serum lutein is a promising biomarker for type 2 diabetes mellitus and diabetic kidney disease in the elderly
title_full_unstemmed Serum lutein is a promising biomarker for type 2 diabetes mellitus and diabetic kidney disease in the elderly
title_short Serum lutein is a promising biomarker for type 2 diabetes mellitus and diabetic kidney disease in the elderly
title_sort serum lutein is a promising biomarker for type 2 diabetes mellitus and diabetic kidney disease in the elderly
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8993643/
https://www.ncbi.nlm.nih.gov/pubmed/35293029
http://dx.doi.org/10.1002/jcla.24350
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