Literature DB >> 29966972

Biochemical investigation of gender-specific association between insulin resistance and inflammatory biomarkers in types 2 diabetic patients.

Muhammad Sajid Hamid Akash1, Kanwal Rehman2, Aamira Liaqat3, Muhammad Numan4, Qaisar Mahmood5, Shagufta Kamal6.   

Abstract

Inflammatory mediators play a key role in the pathogenesis of type 2 diabetes mellitus (T2DM) and development of insulin resistance (IR). The purpose of the present study was to investigate the gender-specific association between serum levels of inflammatory biomarkers and development of IR in type 2 diabetic patients. We recruited 90 study participants and collected their blood samples to measure the serum level of interleukin-6 (IL-6), tumor necrosis factor-alpha (TNF-α), C-reactive protein (CRP), insulin and glucose. We found that the serum levels of IL-6 (< 0.0001), TNF-α (< 0.0001) and CRP (< 0.0001) in type 2 diabetic patients were significantly high as compared to control participants. Moreover, we also found that in female diabetic patients, a significant association was observed between the elevated levels of IL-6 (r = 0.8819, R2 = 0.7778), TNF-α (r = 0.9833, R2 = 0.9669) and CRP (r = 0.9529, R2 = 0.9080) and increased risk of developing IR when compared with that of the serum levels of IL-6 (r = 0.7977, R2 = 0.6364), TNF-α (r = 0.9445, R2 = 0.8920) and CRP (r = 0.9051, R2 = 0.8192) of male diabetic patients. Additionally, we also found that the Body mass index (BMI) of female diabetic patients was strongly correlated (r = 0.9694, R2 = 0.9398) with the increased incidence of IR as compared to that of the BMI (r = 0.9188, R2 = 0.8442) of male diabetic patients. The key findings of present study exhibit that gender differences significantly influence the association of inflammatory biomarkers with the development of IR in T2DM.
Copyright © 2018 Elsevier Masson SAS. All rights reserved.

Entities:  

Keywords:  Diabetes mellitus; Gender-specific association; Inflammatory biomarkers; Insulin resistance

Mesh:

Substances:

Year:  2018        PMID: 29966972     DOI: 10.1016/j.biopha.2018.06.044

Source DB:  PubMed          Journal:  Biomed Pharmacother        ISSN: 0753-3322            Impact factor:   6.529


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