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GSK-3β activation mediates apolipoprotein E4-associated cognitive impairment in type 2 diabetes mellitus: A multicenter, cross-sectional study.
J Diabetes. 2024 Jan; 16(1):e13470.JD

Abstract

AIM

Both the activation of glycogen synthase kinase-3β (GSK-3β) and the presence of ApoE ε4 genotype have been found to respectively correlate with cognitive decline in patients with type 2 diabetes mellitus (T2DM), who further show a high incidence of developing Alzheimer's disease. However, the relationship between ApoE ε4 and GSK-3β in the cognitive impairment of T2DM patients remains unclear.

METHODS

ApoE genotypes and platelet GSK-3β level were measured in 1139 T2DM patients recruited from five medical centers in Wuhan, China. Cognitive functions were assessed by Mini-Mental State Examination (MMSE). The association and the relationships among apolipoprotein E (ApoE) genotypes, GSK-3β activity and cognitive function were analyzed by regression and mediating effect analyses, respectively.

RESULTS

T2DM patients with ApoE ε4 but not ApoE ε2 haplotype showed poorer cognitive function and elevated platelet GSK-3β activity, when using ApoE ε3 as reference. The elevation of GSK-3β activity was positively correlated the diabetes duration, as well as plasma glycated hemoglobin (HbA1c) and glucose levels. Moreover, correlation and regression analysis also revealed significant pairwise correlations among GSK-3β activity, ApoE gene polymorphism and cognitive function. Lastly, using Baron and Kenny modeling, we unveiled a mediative role of GSK-3β activity between ApoE ε4 and cognitive impairment.

CONCLUSION

We reported here that the upregulation of GSK-3β activity mediates the exacerbation of cognitive impairment by ApoE ε4-enhanced cognitive impairment in T2DM patients, suggesting GSK-3β inhibitors as promising drugs for preserving cognitive function in T2DM patients, especially to those with ApoE ε4 genotype.

Authors+Show Affiliations

Department of Pathophysiology, School of Basic Medicine, Ministry of Education Key Laboratory for Neurological Disorders, Hubei Key Laboratory for Neurological Disorders, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China. Department of Radiology, Wuhan Brain Hospital, Wuhan, China.Department of Fundamental Medicine, Wuxi School of Medicine, Jiangnan University, Wuxi, China.Department of Neurosurgery, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.Department of Neurology, Zhongnan Hospital of Wuhan University, Wuhan, China.Department of Pathophysiology, School of Basic Medicine, Ministry of Education Key Laboratory for Neurological Disorders, Hubei Key Laboratory for Neurological Disorders, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.School of Medicine and Health Management, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.Department of Pathophysiology, School of Basic Medicine, Ministry of Education Key Laboratory for Neurological Disorders, Hubei Key Laboratory for Neurological Disorders, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.Li-Yuan Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.Department of Radiology, Wuhan Brain Hospital, Wuhan, China.Department of Pathophysiology, School of Basic Medicine, Ministry of Education Key Laboratory for Neurological Disorders, Hubei Key Laboratory for Neurological Disorders, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.Neuroscience Research Institute and Department of Neurobiology, School of Basic Medical Sciences, Peking University; Key Laboratory for Neuroscience, Ministry of Education/National Health Commission, Peking University, Beijing, China.Department of Pathophysiology, School of Basic Medicine, Ministry of Education Key Laboratory for Neurological Disorders, Hubei Key Laboratory for Neurological Disorders, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China. Co-innovation Center of Neuroregeneration, Nantong University, Nantong, China.

Pub Type(s)

Multicenter Study
Journal Article

Language

eng

PubMed ID

37700547

Citation

Gao, Yang, et al. "GSK-3β Activation Mediates Apolipoprotein E4-associated Cognitive Impairment in Type 2 Diabetes Mellitus: a Multicenter, Cross-sectional Study." Journal of Diabetes, vol. 16, no. 1, 2024, pp. e13470.
Gao Y, Yu H, Liu Y, et al. GSK-3β activation mediates apolipoprotein E4-associated cognitive impairment in type 2 diabetes mellitus: A multicenter, cross-sectional study. J Diabetes. 2024;16(1):e13470.
Gao, Y., Yu, H., Liu, Y., Xu, Z., He, B., Liu, H., Wang, Y., Zhang, Y., Liang, Y., Yang, Y., Zheng, J., & Wang, J. Z. (2024). GSK-3β activation mediates apolipoprotein E4-associated cognitive impairment in type 2 diabetes mellitus: A multicenter, cross-sectional study. Journal of Diabetes, 16(1), e13470. https://doi.org/10.1111/1753-0407.13470
Gao Y, et al. GSK-3β Activation Mediates Apolipoprotein E4-associated Cognitive Impairment in Type 2 Diabetes Mellitus: a Multicenter, Cross-sectional Study. J Diabetes. 2024;16(1):e13470. PubMed PMID: 37700547.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - GSK-3β activation mediates apolipoprotein E4-associated cognitive impairment in type 2 diabetes mellitus: A multicenter, cross-sectional study. AU - Gao,Yang, AU - Yu,Haitao, AU - Liu,Yanchao, AU - Xu,Zhipeng, AU - He,Benrong, AU - Liu,Honghai, AU - Wang,Yuying, AU - Zhang,Yao, AU - Liang,Yi, AU - Yang,Ying, AU - Zheng,Jie, AU - Wang,Jian-Zhi, Y1 - 2023/09/12/ PY - 2023/07/17/revised PY - 2023/05/05/received PY - 2023/08/16/accepted PY - 2024/1/30/medline PY - 2023/9/13/pubmed PY - 2023/9/13/entrez KW - ApoE KW - gene polymorphism KW - glycogen synthase kinase-3β KW - mediation analyses KW - mild cognitive impairment KW - type 2 diabetes mellitus SP - e13470 EP - e13470 JF - Journal of diabetes JO - J Diabetes VL - 16 IS - 1 N2 - AIM: Both the activation of glycogen synthase kinase-3β (GSK-3β) and the presence of ApoE ε4 genotype have been found to respectively correlate with cognitive decline in patients with type 2 diabetes mellitus (T2DM), who further show a high incidence of developing Alzheimer's disease. However, the relationship between ApoE ε4 and GSK-3β in the cognitive impairment of T2DM patients remains unclear. METHODS: ApoE genotypes and platelet GSK-3β level were measured in 1139 T2DM patients recruited from five medical centers in Wuhan, China. Cognitive functions were assessed by Mini-Mental State Examination (MMSE). The association and the relationships among apolipoprotein E (ApoE) genotypes, GSK-3β activity and cognitive function were analyzed by regression and mediating effect analyses, respectively. RESULTS: T2DM patients with ApoE ε4 but not ApoE ε2 haplotype showed poorer cognitive function and elevated platelet GSK-3β activity, when using ApoE ε3 as reference. The elevation of GSK-3β activity was positively correlated the diabetes duration, as well as plasma glycated hemoglobin (HbA1c) and glucose levels. Moreover, correlation and regression analysis also revealed significant pairwise correlations among GSK-3β activity, ApoE gene polymorphism and cognitive function. Lastly, using Baron and Kenny modeling, we unveiled a mediative role of GSK-3β activity between ApoE ε4 and cognitive impairment. CONCLUSION: We reported here that the upregulation of GSK-3β activity mediates the exacerbation of cognitive impairment by ApoE ε4-enhanced cognitive impairment in T2DM patients, suggesting GSK-3β inhibitors as promising drugs for preserving cognitive function in T2DM patients, especially to those with ApoE ε4 genotype. SN - 1753-0407 UR - https://www.unboundmedicine.com/medline/citation/37700547/GSK_3 DB - PRIME DP - Unbound Medicine ER -