Visfatin and Retinol Binding Protein-4 in Young-Onset Type 2 Diabetes Mellitus

Author:

Huang Ya-Li12ORCID,Chen Yen-Lin3ORCID,Lin Jiunn-Diann45ORCID,Pei Dee67ORCID,Pitrone Pietro8ORCID,Chen Jin-Shuen91011ORCID,Wu Chung-Ze45ORCID

Affiliation:

1. Department of Public Health, School of Medicine, College of Medicine, Taipei Medical University, Taipei City 11031, Taiwan

2. School of Public Health, College of Public Health, Taipei Medical University, Taipei City 11031, Taiwan

3. Department of Pathology, Tri-Service General Hospital, National Defense Medical Center, Taipei City 11490, Taiwan

4. Division of Endocrinology and Metabolism, Department of Internal Medicine, School of Medicine, College of Medicine, Taipei Medical University, Taipei City 11031, Taiwan

5. Division of Endocrinology and Metabolism, Department of Internal Medicine, Shuang Ho Hospital, Taipei Medical University, New Taipei City 23561, Taiwan

6. School of Medicine, College of Medicine, Fu Jen Catholic University, New Taipei City 24352, Taiwan

7. Division of Endocrinology and Metabolism, Department of Internal Medicine, Fu Jen Catholic University Hospital, New Taipei City 24352, Taiwan

8. Radiology Department, Papardo Hospital, 98100 Messina, Italy

9. Deputy Superintendent, Kaohsiung Veterans General Hospital, Kaohsiung City 81362, Taiwan

10. Institute of Precision Medicine, National Sun Yat-sen University, Kaohsiung City 80424, Taiwan

11. Division of Nephrology, Department of Medicine, Tri-Service General Hospital, Taipei City 11490, Taiwan

Abstract

Background and Objectives: The prevalence of type 2 diabetes mellitus in adolescents has increased rapidly in recent decades. However, the role of adipokines on pathophysiology in young-onset type 2 diabetes mellitus (YDM) is not clear. In this article, we explored the relationships between the adipokines (visfatin and retinol binding protein 4 (RBP4)) and metabolic syndrome (MetS) components in both YDM and late-onset type 2 diabetes mellitus (ODM). Materials and Methods: There were 36 patients with YDM (23.6 ± 4.8 years) and 36 patients with ODM (54.3 ± 10.1 years) enrolled. Visfatin, RBP4, and MetS components were measured. The relationships between visfatin, RBP4 and MetS components were assessed in YDM and ODM. Results: The visfatin, but not the RPB4 level, was significantly higher in YDM than in ODM. After adjusting for age and body mass index, visfatin was not related to any MetS components except that there was a negative correlation with fasting plasma glucose (FPG). As for RPB4, triglyceride was found to be positively and FPG negatively related to RBP4 in YDM. However, in ODM, the only positive relationship that existed was between RBP4 and diastolic blood pressure. Conclusions: In conclusion, both visfatin and RBP4 had certain roles in diabetes and MetS although their relationships were different in YDM and ODM. Further studies are needed to explore their physiological and pathological effects in glucose metabolism.

Funder

Taipei Medical University-Shuang Ho Hospital

Publisher

MDPI AG

Subject

General Medicine

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