A cross-sectional study to assess beta cell function in individuals with recently diagnosed young onset type 2 diabetes mellitus and its complications.

Abstract

The primary objective of this study was to assess beta cell function of recently diagnosed young onset type 2 diabetes mellitus (T2DM) individuals. The secondary objective examined the association between C- peptide with metabolic factors and diabetes complications. A cross-sectional study was conducted for young onset T2DM individuals aged 18-35 years with disease duration not more than 5 years. Plasma basal and stimulated C-peptide was measured before and after intravenous glucagon injection.  Demographic data, medical history and complications were obtained from medical records and clinical assessment. A total of 113 participants with young onset T2DM with mean age of 29 years and median disease duration of 24 months were included in this study. The median (interquartile range) basal and stimulated C-peptide was 619 (655) pmol/L and 1231(1024) pmol/L . Adequate beta cell function was present in 78-86% of the participants based on the basal and stimulated C-peptide levels. Obesity and hypertension were independently associated with higher basal and stimulated C-peptide while diabetic kidney disease was independently associated with higher basal C-peptide. We found most recently diagnosed young onset T2DM have adequate beta cell function. Elevated C-peptide levels associated with obesity, hypertension and diabetic kidney disease suggests insulin resistance as the key driving factor for complications.

Competing Interest Statement

The authors have declared no competing interest.

Funding Statement

This study was funded by a diabetes and endocrine subspecialty research grant awarded to the primary author , Dr Shamharini Nagaratnam by the Malaysian Endocrine and Metabolic Society (MEMS). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

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The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

his study was approved by the Medical Research and Ethics Committee (MREC) of Ministry of Health Malaysia (MOH),National Medical Research Registry (NMMR) ID : NMRR-19-1048-47849.

I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.

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I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

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Data Availability

All relevant data are within the manuscript and its supporting information files

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