PMID- 33658784 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20240331 IS - 1176-6328 (Print) IS - 1178-2021 (Electronic) IS - 1176-6328 (Linking) VI - 17 DP - 2021 TI - Peripheral Polyneuropathy and Cognitive Impairment in Type II Diabetes Mellitus. PG - 627-635 LID - 10.2147/NDT.S284308 [doi] AB - BACKGROUND: Neuropathy is one of most common complications in diabetic patients. Diagnosis of diabetic neuropathy is essential for decreasing the rate of the disability and death. Neuron-specific enolase (NSE) is released from damaged neuronal cells and enters the blood circulation through an injured blood brain barrier. Therefore, serum NSE can reflect the damage of neurons and brain tissue. OBJECTIVE: To evaluate peripheral polyneuropathy and cognitive function in Type 2 Diabetes Mellitus (T2DM) and correlate them with NSE level as a possible biomarker of diabetic neuropathy. SUBJECTS AND METHODS: Forty five T2DM patients with polyneuropathy were randomly recruited in this study compared to 45 healthy age and sex matched subjects as a control. Patients group were divided into two subgroups, 24 diabetic patients with painful peripheral neuropathy and 21 with painless peripheral neuropathy. All were subjected to clinical assessment by diabetic neuropathy symptom score, Dyck neuropathy grading, Mini-Mental State Examination (MMSE), assessment of HbA1c, NSE biomarker and neurophysiological assessment (nerve conduction study (NCS), event related potential (P300wave) and somatosensory evoked potential (SSEP) of the right median nerve). RESULTS: There were significant decrease in cognitive functions in diabetic patients compared to controls and a significant increase in NSE in diabetic patients. There were no significant difference between patients with painless and painful diabetic neuropathy as regard MMSE, HbA1c and NSE. There were significant correlation of P300 in diabetic patients with HbA1c and NSE. CONCLUSION: Neurophysiological assessment of diabetic patients by NCS, SSEP and P300 have well evaluation of cognitive functions, painless, and painful diabetic polyneuropathy. NSE is a beneficial biomarker in diabetic patients to pick up neurological complications. CI - (c) 2021 Elsharkawy et al. FAU - Elsharkawy, Rasha Elbialy AU - Elsharkawy RE AD - Department of Neurology, Faculty of Medicine for Girls, Al-Azhar University, Cairo, Egypt. FAU - Abdel Azim, Ghada Saed AU - Abdel Azim GS AUID- ORCID: 0000-0002-2289-3802 AD - Department of Neurology, Faculty of Medicine for Girls, Al-Azhar University, Cairo, Egypt. FAU - Osman, Marwa Abdellah AU - Osman MA AD - Department of Neurology, Faculty of Medicine for Girls, Al-Azhar University, Cairo, Egypt. FAU - Maghraby, Hend Maghraby AU - Maghraby HM AUID- ORCID: 0000-0001-7224-2242 AD - Department of Internal Medicine, Faculty of Medicine for Girls, Al-Azhar University, Cairo, Egypt. FAU - Mohamed, Rehab Abdelfattah AU - Mohamed RA AUID- ORCID: 0000-0003-0760-5013 AD - Department of Internal Medicine, Faculty of Medicine for Girls, Al-Azhar University, Cairo, Egypt. FAU - Abdelsalam, Eman Mahmoud AU - Abdelsalam EM AUID- ORCID: 0000-0001-9695-0470 AD - Department of Internal Medicine, Faculty of Medicine for Girls, Al-Azhar University, Cairo, Egypt. FAU - Ebrahem, Eman Elshohat AU - Ebrahem EE AD - Department of Biochemistry, Faculty of Medicine for Girls, Al-Azhar University, Cairo, Egypt. FAU - Seliem, Nora Mohamed Ahmed AU - Seliem NMA AUID- ORCID: 0000-0001-9541-6479 AD - Department of Biochemistry, Faculty of Medicine for Girls, Al-Azhar University, Cairo, Egypt. LA - eng PT - Journal Article DEP - 20210224 PL - New Zealand TA - Neuropsychiatr Dis Treat JT - Neuropsychiatric disease and treatment JID - 101240304 PMC - PMC7917357 OTO - NOTNLM OT - MMSE OT - Mini-Mental State Examination OT - NSE OT - diabetic neuropathy OT - glycated hemoglobin OT - nerve conduction study OT - neuron-specific enolase COIS- The authors declared no conflicts of interest in this work. EDAT- 2021/03/05 06:00 MHDA- 2021/03/05 06:01 PMCR- 2021/02/24 CRDT- 2021/03/04 05:53 PHST- 2020/10/03 00:00 [received] PHST- 2020/12/24 00:00 [accepted] PHST- 2021/03/04 05:53 [entrez] PHST- 2021/03/05 06:00 [pubmed] PHST- 2021/03/05 06:01 [medline] PHST- 2021/02/24 00:00 [pmc-release] AID - 284308 [pii] AID - 10.2147/NDT.S284308 [doi] PST - epublish SO - Neuropsychiatr Dis Treat. 2021 Feb 24;17:627-635. doi: 10.2147/NDT.S284308. eCollection 2021.