PMID- 35180824 OWN - NLM STAT- MEDLINE DCOM- 20220222 LR - 20220222 IS - 1336-0329 (Electronic) IS - 1210-0668 (Linking) VI - 56 IP - 1 DP - 2022 Feb 18 TI - Insulin receptor substrate 1 gene variations and lipid profile characteristics in the type 2 diabetic patients with comorbid obesity and chronic pancreatitis. PG - 1-9 LID - 10.2478/enr-2022-0001 [doi] AB - Objective. Type 2 diabetes mellitus (T2DM) is one of diseases that develops in a setting of polymorbid processes or more often promotes their development, forming in this spectrum the phenomenon of comorbidity. The aim of this study was to evaluate changes in the lipid panel data in T2DM patients with comorbid obesity and chronic pancreatitis (CP) taking into account the C/A polymorphism of the insulin receptor substrate 1 (IRS1) gene (rs2943640). Methods. The study involved 34 T2DM patients and 10 healthy individuals. The rs2943640 IRS1 gene polymorphism was genotyped using the TaqMan real-time polymerase chain reaction (PCR) method. Blood serum lipid panel data were determined with commercially available kits on a Cobas 6000 analyzer. Results. In patients with only T2DM and T2DM + comorbid obesity, an association between IRS1 gene polymorphism (rs2943640) and lipid profile abnormalities with maximum changes of the lipid characteristics recorded in C/C genotype carriers was found. Within the C/C genotype of the IRS1 gene (rs2943640) in type 2 diabetic patients with comorbid obesity and CP, significantly lower high-density lipoprotein cholesterol (HDL-C) levels and significantly higher levels of triglycerides (TG), non-HDL-C and remnant cholesterol (RC) in relation to type 2 diabetic patients with comorbid obesity were found. At the same time, within the C/A genotype of the IRS1 gene (rs2943640), significant changes of lipid panel data were found in type 2 diabetic patients with comorbid obesity relative to the control group (p<0.001). Conclusions. Our data indicate that the presence of the C allele of IRS1 gene (rs2943640) in both homozygous and heterozygous states may indicate increased risk of dyslipidemia in type 2 diabetic patients with comorbidities. CI - (c) 2022 Mariya Marushchak et al., published by Sciendo. FAU - Marushchak, Mariya AU - Marushchak M AD - Department of Functional and Laboratory Diagnostics, I. Horbachevsky Ternopil National Medical University, Ternopil, Ukraine. FAU - Hevko, Uliana AU - Hevko U AD - Department of Functional and Laboratory Diagnostics, I. Horbachevsky Ternopil National Medical University, Ternopil, Ukraine. FAU - Krynytska, Inna AU - Krynytska I AD - Department of Functional and Laboratory Diagnostics, I. Horbachevsky Ternopil National Medical University, Ternopil, Ukraine. LA - eng PT - Journal Article DEP - 20220218 PL - Germany TA - Endocr Regul JT - Endocrine regulations JID - 9112018 RN - 0 (Cholesterol, HDL) RN - 0 (Insulin Receptor Substrate Proteins) SB - IM MH - Cholesterol, HDL MH - Comorbidity MH - *Diabetes Mellitus, Type 2/epidemiology/genetics MH - Humans MH - Insulin Receptor Substrate Proteins/genetics MH - Obesity/epidemiology/genetics MH - *Pancreatitis, Chronic OTO - NOTNLM OT - IRS1 gene OT - comorbidities OT - lipid profile OT - type 2 diabetes mellitus EDAT- 2022/02/19 06:00 MHDA- 2022/02/23 06:00 CRDT- 2022/02/18 20:16 PHST- 2022/02/19 06:00 [pubmed] PHST- 2022/02/23 06:00 [medline] PHST- 2022/02/18 20:16 [entrez] AID - enr-2022-0001 [pii] AID - 10.2478/enr-2022-0001 [doi] PST - epublish SO - Endocr Regul. 2022 Feb 18;56(1):1-9. doi: 10.2478/enr-2022-0001.