PMID- 33081726 OWN - NLM STAT- MEDLINE DCOM- 20210201 LR - 20210201 IS - 1471-2261 (Electronic) IS - 1471-2261 (Linking) VI - 20 IP - 1 DP - 2020 Oct 20 TI - Increased osteoprotegerin level is associated with impaired cardiovagal modulation in type-2 diabetic patients treated with oral antidiabetic drugs. PG - 453 LID - 10.1186/s12872-020-01729-1 [doi] LID - 453 AB - BACKGROUND: An increased osteoprotegerin (OPG) level has been reported in both type-2 diabetes mellitus (T2DM) and cardiovascular diease (CVD) that are linked to sympathovagal imbalance (SVI). We explored the link of osteoprotegerin with cardiovagal modulation in T2DM. METHODS: We assessed fasting serum OPG, high-sensitive C-reactive protein (hsCRP), glucose, insulin and lipid profile in patients having T2DM receiving oral antidiabetic drugs (OAD) (n = 42) compared with age, gender and body composition-matched healthy participants without diabetes (n = 42). Rate pressure product (RPP), spectral indices of heart rate variability (HRV) and body composition were recorded in both the groups. Association of HOMA-IR and OPG with various parameters were assessed. RESULTS: Osteoprotegerin, HOMA-IR, hsCRP, coronary lipid risk factor were significantly increased, markers of cardiovagal modulation (TP, SDNN, RMSSD) were considerably decreased, ratio of low-frequency to high-frequency (LH-HF ratio), the indicator of SVI, and RPP, the marker of myocardial work stress were significantly higher in patients with diabetes, suggesting an overall elevated CVD risks in them. HOMA-IR was correlated with RMSSD, lipid risk factors and OPG. Rise in OPG was correlated with decreased cardiovagal modulation in patients with diabetes. There was significant contribution of OPG in decreasing TP, suggesting impaired cardiovagal modulation. CONCLUSION: T2DM patients receiving OAD had higher cardiometabolic risks compared to age, gender and body composition-matched healthy individuals. Increased level of OPG is linked to decreased cardiovagal modulation in T2DM patients. FAU - Jasmine, M R AU - Jasmine MR AD - Department of Biochemistry, Jawaharlal Institute of Postgraduate Medical Education and Research (JIPMER), Puducherry, 605 006, India. FAU - Nanda, Nivedita AU - Nanda N AUID- ORCID: 0000-0002-8887-8357 AD - Department of Biochemistry, Jawaharlal Institute of Postgraduate Medical Education and Research (JIPMER), Puducherry, 605 006, India. drnnivedita@gmail.com. FAU - Sahoo, Jayaprakash AU - Sahoo J AD - Department of Endocrinology, Jawaharlal Institute of Postgraduate Medical Education and Research, Puducherry, India. FAU - Velkumary, S AU - Velkumary S AD - Department of Physiology, Jawaharlal Institute of Postgraduate Medical Education and Research, Puducherry, India. FAU - Pal, G K AU - Pal GK AD - Department of Physiology, Jawaharlal Institute of Postgraduate Medical Education and Research, Puducherry, India. LA - eng GR - JIP/Res/Intra-MSc/02//2015-16/Intramural/International PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20201020 PL - England TA - BMC Cardiovasc Disord JT - BMC cardiovascular disorders JID - 100968539 RN - 0 (Biomarkers) RN - 0 (Hypoglycemic Agents) RN - 0 (Osteoprotegerin) RN - 0 (Sulfonylurea Compounds) RN - 0 (TNFRSF11B protein, human) RN - 6KY687524K (glimepiride) RN - 9100L32L2N (Metformin) SB - IM MH - Administration, Oral MH - Adult MH - Biomarkers/blood MH - Cardiometabolic Risk Factors MH - Case-Control Studies MH - Diabetes Mellitus, Type 2/blood/*drug therapy/physiopathology MH - Female MH - Heart/*innervation MH - Humans MH - Hypoglycemic Agents/*administration & dosage/adverse effects MH - India MH - Male MH - Metformin/*administration & dosage/adverse effects MH - Middle Aged MH - Osteoprotegerin/*blood MH - Risk Assessment MH - Sulfonylurea Compounds/*administration & dosage/adverse effects MH - Treatment Outcome MH - Up-Regulation MH - Vagus Nerve/*physiopathology PMC - PMC7574185 OTO - NOTNLM OT - Cardiometabolic risks OT - Cardiovagal modulation OT - Heart rate variability OT - Osteoprotegerin OT - Sympathovagal imbalance OT - Type-2 diabetes mellitus COIS- The authors declare that there is no competing interest. EDAT- 2020/10/22 06:00 MHDA- 2021/02/02 06:00 PMCR- 2020/10/20 CRDT- 2020/10/21 05:37 PHST- 2020/02/10 00:00 [received] PHST- 2020/10/06 00:00 [accepted] PHST- 2020/10/21 05:37 [entrez] PHST- 2020/10/22 06:00 [pubmed] PHST- 2021/02/02 06:00 [medline] PHST- 2020/10/20 00:00 [pmc-release] AID - 10.1186/s12872-020-01729-1 [pii] AID - 1729 [pii] AID - 10.1186/s12872-020-01729-1 [doi] PST - epublish SO - BMC Cardiovasc Disord. 2020 Oct 20;20(1):453. doi: 10.1186/s12872-020-01729-1.