PMID- 28951620 OWN - NLM STAT- MEDLINE DCOM- 20190716 LR - 20221207 IS - 2045-2322 (Electronic) IS - 2045-2322 (Linking) VI - 7 IP - 1 DP - 2017 Sep 26 TI - Lipoprotein-associated Phospholipase A2 Is Associated with Risk of Mild Cognitive Impairment in Chinese Patients with Type 2 Diabetes. PG - 12311 LID - 10.1038/s41598-017-12515-z [doi] LID - 12311 AB - Type 2 diabetes mellitus (T2DM) is a low-grade chronic inflammatory diseases, which have been implicated in the pathogenesis of cognitive decline. We aim to evaluate associations between inflammatory markers and the risk of mild cognitive impairment (MCI) in T2DM. This study of 140 diabetic patients involved 71 with MCI and 69 controls. Clinical parameters, neuropsychological tests, high sensitivity C reactive protein (hsCRP), interleukin-6 (IL-6), lipoprotein-associated Phospholipase A2 (Lp-PLA2) mass and activity were measured. The results showed significantly higher plasma hsCRP, IL-6, Lp-PLA2 mass and activity in MCI group compared to controls. In T2DM with MCI, the Montreal Cognitive Assessment (MoCA) score was positively correlated with education level and high-density lipoprotein cholesterol (HDL-c), but inversely correlated with age, glycosylated hemoglobin, intima-media thickness (IMT), hsCRP, IL-6, and Lp-PLA2 mass and activity. Correlation analysis showed that both plasma Lp-PLA2 mass and activity were positively correlated with total cholesterol, low-density lipoprotein cholesterol, and IMT but negatively associated with MoCA score. Multivariable logistic regression analysis indicated higher hsCRP, Lp-PLA2 mass, Lp-PLA2 activity, and lower HDL-c to be independent risk factors increasing the possibility of MCI in T2DM. In conclusion, plasma Lp-PLA2 and hsCRP were found to be associated with the risk of MCI among T2DM patients. FAU - Cai, Rongrong AU - Cai R AD - Department of Endocrinology, The Affiliated ZhongDa Hospital of Southeast University, Nanjing, China. AD - Medical school of Southeast University, Nanjing, China. FAU - Huang, Rong AU - Huang R AD - Department of Endocrinology, The Affiliated ZhongDa Hospital of Southeast University, Nanjing, China. FAU - Han, Jing AU - Han J AD - Department of Endocrinology, The Affiliated ZhongDa Hospital of Southeast University, Nanjing, China. FAU - Sun, Haixia AU - Sun H AD - Department of Endocrinology, Yixing People's Hospital, Yixing, China. FAU - Sun, Jie AU - Sun J AD - Department of Endocrinology, The Affiliated ZhongDa Hospital of Southeast University, Nanjing, China. FAU - Xia, Wenqing AU - Xia W AD - Department of Endocrinology, Nanjing First Hospital, Nanjing Medical University, Nanjing, China. FAU - Tian, Sai AU - Tian S AD - Department of Endocrinology, The Affiliated ZhongDa Hospital of Southeast University, Nanjing, China. FAU - Dong, Xue AU - Dong X AD - Department of Endocrinology, Wuxi No.2 People's Hospital, Wuxi, China. FAU - Shen, Yanjue AU - Shen Y AD - Department of Endocrinology, The Affiliated ZhongDa Hospital of Southeast University, Nanjing, China. FAU - Wang, Shaohua AU - Wang S AD - Department of Endocrinology, The Affiliated ZhongDa Hospital of Southeast University, Nanjing, China. gyjwsh@163.com. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20170926 PL - England TA - Sci Rep JT - Scientific reports JID - 101563288 RN - 0 (Biomarkers) RN - 9007-41-4 (C-Reactive Protein) RN - EC 3.1.1.47 (1-Alkyl-2-acetylglycerophosphocholine Esterase) RN - EC 3.1.1.47 (PLA2G7 protein, human) SB - IM MH - 1-Alkyl-2-acetylglycerophosphocholine Esterase/*blood/metabolism MH - Adult MH - Aged MH - Asian People MH - Biomarkers/blood MH - C-Reactive Protein/analysis/metabolism MH - Case-Control Studies MH - Cognitive Dysfunction/*blood/etiology MH - Diabetes Mellitus, Type 2/blood/*complications MH - Female MH - Humans MH - Male MH - Middle Aged MH - Risk Factors PMC - PMC5615059 COIS- The authors declare that they have no competing interests. EDAT- 2017/09/28 06:00 MHDA- 2019/07/17 06:00 PMCR- 2017/09/26 CRDT- 2017/09/28 06:00 PHST- 2016/09/05 00:00 [received] PHST- 2017/09/12 00:00 [accepted] PHST- 2017/09/28 06:00 [entrez] PHST- 2017/09/28 06:00 [pubmed] PHST- 2019/07/17 06:00 [medline] PHST- 2017/09/26 00:00 [pmc-release] AID - 10.1038/s41598-017-12515-z [pii] AID - 12515 [pii] AID - 10.1038/s41598-017-12515-z [doi] PST - epublish SO - Sci Rep. 2017 Sep 26;7(1):12311. doi: 10.1038/s41598-017-12515-z.