Serum FGF-21 levels in individuals with prediabetes and newly diagnosed type 2 diabetes mellitus

Aim:To compare serum fibroblast growth factor-21 (FGF-21) levels in healthy individuals, patients with impaired fasting glucose (IFG) and impaired glucose tolerance (IGT);combined prediabetic patients (IFG+IGT), and patients with newly diagnosed type 2 diabetes mellitus (T2DM). In addition, the rela...

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Veröffentlicht in:Experimental Biomedical Research 2022-04, Vol.5 (2), p.225
Hauptverfasser: Gurler, Mujgan, Dag, Ismail, Serin, Naciye Ozden
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Sprache:eng
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Zusammenfassung:Aim:To compare serum fibroblast growth factor-21 (FGF-21) levels in healthy individuals, patients with impaired fasting glucose (IFG) and impaired glucose tolerance (IGT);combined prediabetic patients (IFG+IGT), and patients with newly diagnosed type 2 diabetes mellitus (T2DM). In addition, the relationship between serum FGF-21 levels and demographic characteristics, glucose metabolism and laboratory parameters predicting cardiovascular disease risk factors were investigated.Method: Age, gender, waist and hip circumference measurements, and body mass index (BMI) values were reported for all study groups. Fasting serum insulin, c-peptide levels, insulin/c-peptide ratio, homeostatic model assessment for insulin resistance(HOMA-IR)value, serum lipids, serum cortisol, and plasma fibrinogen levels were all evaluated.Result: There were no statistically significant variations in the gender distribution of male and female groups (p= 0.340). For age, BMI, waist and hip circumference, no statistically significant differences were observed between groups 2, 3, and 4. When the groups were compared for FGF-21 levels, moderate differences were found between Groups 1 and 2 (p= 0.04), highly significant differences between Groups 1 and 3 (p0.05).Conclusions: Serum FGF-21 levels were significantly increased in prediabetic patients and T2DM. Furthermore, FGF-21 levels were linked to a rise in cardiovascular risk factors. It may shed light onthe etiopathogenesis of glucometabolic diseases.
ISSN:2618-6454
2618-6454
DOI:10.30714/j-ebr.2022275837