Circulatory Omentin-1 levels but not genetic variants influence the pathophysiology of Type 2 diabetes. (July 2019)
- Record Type:
- Journal Article
- Title:
- Circulatory Omentin-1 levels but not genetic variants influence the pathophysiology of Type 2 diabetes. (July 2019)
- Main Title:
- Circulatory Omentin-1 levels but not genetic variants influence the pathophysiology of Type 2 diabetes
- Authors:
- Rathwa, Nirali
Patel, Roma
Pramanik Palit, Sayantani
Jadeja, Shahnawaz D.
Narwaria, Mahendra
Ramachandran, A.V.
Begum, Rasheedunnisa - Abstract:
- Highlights: No association has been found between Omentin-1 polymorphisms and risk of T2D susceptibility. Omentin-1 rs2274907 AT genotype is associated with BMI. Elevated Omentin-1 transcript levels are observed in T2D patients. Reduced circulatory Omentin-1 levels are seen in T2D patients. Abstract: Objective: Omentin-1, an anti-inflammatory protein, is secreted by the visceral adipose tissue. Altered levels of Omentin-1 are associated with obesity and Type 2 Diabetes (T2D). Although Omentin-1 is implicated in the insulin signaling pathway, the relationship between the genetic variants of Omentin-1 and T2D is not yet explored. The current study evaluates the association of Omentin-1 polymorphisms (rs2274907 A/T and rs1333062 G/T), its transcript and protein levels, and genotype-phenotype correlation with metabolic parameters and T2D susceptibility. Methods: Plasma and Peripheral Blood Mononuclear Cells (PBMCs) were separated from venous blood taken from 250 controls and 250 T2D patients recruited from Gujarat, India. Genomic DNA was isolated from PBMCs and genotyping of Omentin-1 variants was performed by Polymerase Chain Reaction-Restriction Fragment Length Polymorphism (PCR-RFLP). RNA was isolated from Visceral Adipose Tissue (VAT) samples of 12 controls and 10 patients, and transcript levels of Omentin-1 were assessed by qPCR. Plasma Omentin-1 levels were estimated by ELISA. Fasting Blood Glucose, Body Mass Index (BMI) and plasma lipid profile were considered for theHighlights: No association has been found between Omentin-1 polymorphisms and risk of T2D susceptibility. Omentin-1 rs2274907 AT genotype is associated with BMI. Elevated Omentin-1 transcript levels are observed in T2D patients. Reduced circulatory Omentin-1 levels are seen in T2D patients. Abstract: Objective: Omentin-1, an anti-inflammatory protein, is secreted by the visceral adipose tissue. Altered levels of Omentin-1 are associated with obesity and Type 2 Diabetes (T2D). Although Omentin-1 is implicated in the insulin signaling pathway, the relationship between the genetic variants of Omentin-1 and T2D is not yet explored. The current study evaluates the association of Omentin-1 polymorphisms (rs2274907 A/T and rs1333062 G/T), its transcript and protein levels, and genotype-phenotype correlation with metabolic parameters and T2D susceptibility. Methods: Plasma and Peripheral Blood Mononuclear Cells (PBMCs) were separated from venous blood taken from 250 controls and 250 T2D patients recruited from Gujarat, India. Genomic DNA was isolated from PBMCs and genotyping of Omentin-1 variants was performed by Polymerase Chain Reaction-Restriction Fragment Length Polymorphism (PCR-RFLP). RNA was isolated from Visceral Adipose Tissue (VAT) samples of 12 controls and 10 patients, and transcript levels of Omentin-1 were assessed by qPCR. Plasma Omentin-1 levels were estimated by ELISA. Fasting Blood Glucose, Body Mass Index (BMI) and plasma lipid profile were considered for the genotype-phenotype correlation analysis. Results: Our study revealed no association of Omentin-1 genetic variants with T2D risk ( p > 0.05). However, the AT genotype of Omentin-1 rs2274907 A/T polymorphism was associated with increased BMI ( p = 0.0247). Plasma Omentin-1 levels were significantly decreased ( p < 0.0001) however, increased VAT Omentin-1 transcript levels ( p = 0.0127) were observed in T2D patients. Conclusion: Our findings suggest that decreased circulatory Omentin-1 levels could pose a risk towards T2D susceptibility. … (more)
- Is Part Of:
- Cytokine. Volume 119(2019)
- Journal:
- Cytokine
- Issue:
- Volume 119(2019)
- Issue Display:
- Volume 119, Issue 2019 (2019)
- Year:
- 2019
- Volume:
- 119
- Issue:
- 2019
- Issue Sort Value:
- 2019-0119-2019-0000
- Page Start:
- 144
- Page End:
- 151
- Publication Date:
- 2019-07
- Subjects:
- Obesity -- Single nucleotide polymorphism -- Linkage disequilibrium -- Haplotype -- Genotype-phenotype correlation
T2D Type 2 Diabetes -- FBG Fasting Blood Glucose -- TC Total Cholesterol -- HDL High Density Lipoprotein -- TG Triglycerides -- LDL Low Density Lipoprotein -- BMI Body Mass Index -- PCR-RFLP Polymerase Chain Reaction-Restriction Fragment Length Polymorphism
Cytokines -- Periodicals
571.844 - Journal URLs:
- http://www.sciencedirect.com/science/journal/10434666 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.cyto.2019.03.011 ↗
- Languages:
- English
- ISSNs:
- 1043-4666
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3506.778000
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British Library HMNTS - ELD Digital store - Ingest File:
- 26024.xml