Circulating Betatrophin and Hepatocyte Growth Factor in Type 2 Diabetic Patients: Their Relationship With Disease Prognosis

Abdulrahman Abdulwahab Alduraywish


Background: In Saudi Arabia, diabetes established itself as an epidemic that necessitates dissection of its predisposing factors and pathogenesis to set appropriate preventive measures. In a cross-sectional study, relationships between plasma betatrophin (BetaT) and hepatocyte growth factor (HGF) on one side, and, glycemic control, lipogram, anthropometric indices, treatment and prognosis on the other side were assessed in Saudi patients with type 2 diabetes mellitus (T2DM) vs. healthy controls.

Methods: The study voluntarily enrolled 202 T2DM patients (44 males and 158 females) and socioeconomically, age- and body mass index (BMI)-matched 106 healthy participants (71 males and 35 females). All participants were subgrouped according to gender and BMI (< 25 and ? 25) and patients were also subgrouped according to disease duration (? 5 and > 5 years) and treatment (insulin/non-insulin). Demographic and anthropometric data were anonymously collected. EDTA whole blood for HbA1c and its plasma for bioassays were frozen at -80 °C. Standard procedures and specific immunoassays were employed for biomarkers.

Results: Plasma insulin paralleled BMI and disease duration and was highly significantly different comparing patients and healthy controls. As expected glycemic control and lipogram indices were also highly significantly different comparing patients and healthy controls. Because of the massive individual variation in the plasma levels of each of betatrophin (except for a higher level in patients with lower BMI) and HGF (except for a higher level in females and those with higher BMI among controls), there were non-significant differences comparing patients and healthy controls. Males were more inclined to have more insulin treatment. Surprisingly, the later doubled the disease severity complication score and correlated negatively with plasma HDL-cholesterol. Betatrophin did not show much correlation among controls but correlated negatively with age and cholesterol and positively with BMI and HbA1c in patients. HGF showed very clear negative correlation with age and plasma insulin in patients.

Conclusion: The massive individual variation in plasma content of betatrophin and HGF did allow specific diagnostic/pathogenetic classification for these two hepato-/adipokines. This may reflect gene polymorphism at their gene regulatory sequences and/or resistance correlating insulin resistance. The former is being pursued in our laboratory for patients with distinctly higher and lower levels.

J Endocrinol Metab. 2017;7(1):31-43



Betatrophin; Hepatocyte growth factor; Type 2 diabetes mellitus; Disease prognosis; Saudi Arabia

Full Text: HTML PDF
Home     |     Log In     |      About     |      Search     |      Current     |      Archives     |      Submit      |     Subscribe



Aims and Scope

Current Issues

Conflict of Interest

About Publisher

Editorial Board



Company Profile

Editorial Office

Misconduct and Retraction


Company Registration

Contact Us

Abstracting and Indexing



Instructions to Authors


Declaration of Helsinki

Contact Publisher

Submission Checklist


Terms of Use

Company Address

Submit a Manuscript

Open Access Policy

Privacy Policy

Browse Journals

Publishing Fee

Publishing Policy


Recent Highlights

Peer-Review Process

Publishing Quality

Code of Ethics

Advertising Policy

Manuscript Tracking

Advanced Search

For Librarians


Publishing Process

Publication Frequency

For Reviewers

Propose a New Journal


Journal of Endocrinology and Metabolism, bimonthly, ISSN 1923-2861 (print), 1923-287X (online), published by Elmer Press Inc.        
The content of this site is intended for health care professionals.
This is an open-access journal distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License, which permits unrestricted
non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Creative Commons Attribution license (Attribution-NonCommercial 4.0 International CC-BY-NC 4.0)

This journal follows the International Committee of Medical Journal Editors (ICMJE) recommendations for manuscripts submitted to biomedical journals,
the Committee on Publication Ethics (COPE) guidelines, and the Principles of Transparency and Best Practice in Scholarly Publishing.

website:   editorial contact:
Address: 9225 Leslie Street, Suite 201, Richmond Hill, Ontario, L4B 3H6, Canada

© Elmer Press Inc. All Rights Reserved.