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Letter to the Editor
©The Author(s) 2025. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Clin Cases. Jan 6, 2025; 13(1): 93632
Published online Jan 6, 2025. doi: 10.12998/wjcc.v13.i1.93632
Intricacies during pregnancy with gestational diabetes mellitus
Ripunjay Prasad, Arvind Kumar Morya, Parul Chawla Gupta, Rimesh Pal, Richa Rattan
Richa Rattan, Rimesh Pal, Department of Endocrinology, Post Graduate Institute of Medical Education and Research, Chandigarh 160012, India
Parul Chawla Gupta, Department of Ophthalmology, Post Graduate Institute of Medical Education and Research, Chandigarh 160012, Punjab, India
Arvind Kumar Morya, Department of Ophthalmology, All India Institute of Medical Sciences, Hyderabad 508126, Telangana, India
Ripunjay Prasad, Department of Ophthalmology, RP Eye Institute, Delhi 110001, India
Author contributions: Morya AK, Rattan R, and Pal R designed the study; Rattan R, Pal R, Gupta PC, and Morya AK wrote the manuscript; Prasad R edited the manuscript; all of the authors read and approved the final version of the manuscript to be published.
Conflict-of-interest statement: All the authors declare that they have no conflict of interest.
Corresponding author: Arvind Kumar Morya, Doctor, MS, Neurosurgeon, Professor, Surgeon, Department of Ophthalmology, All India Institute of Medical Sciences, Bibi Nagar, Hyderabad 508126, Telangana, India. bulbul.morya@gmail.com
Received: March 2, 2024
Revised: September 22, 2024
Accepted: October 23, 2024
Published online: January 6, 2025
Processing time: 249 Days and 14.8 Hours
Abstract

The study by Cao et al aimed to identify early second-trimester biomarkers that could predict gestational diabetes mellitus (GDM) development using advanced proteomic techniques, such as Isobaric tags for relative and absolute quantitation isobaric tags for relative and absolute quantitation and liquid chromatography-mass spectrometry liquid chromatography-mass spectrometry. Their analysis revealed 47 differentially expressed proteins in the GDM group, with retinol-binding protein 4 and angiopoietin-like 8 showing significantly elevated serum levels compared to controls. Although these findings are promising, the study is limited by its small sample size (n = 4 per group) and lacks essential details on the reproducibility and reliability of the protein quantification methods used. Furthermore, the absence of experimental validation weakens the interpretation of the protein-protein interaction network identified through bioinformatics analysis. The study's focus on second-trimester biomarkers raises concerns about whether this is a sufficiently early period to implement preventive interventions for GDM. Predicting GDM risk during the first trimester or pre-conceptional period may offer more clinical relevance. Despite its limitations, the study presents valuable insights into potential GDM biomarkers, but larger, well-validated studies are needed to establish their predictive utility and generalizability.

Keywords: Gestational diabetes mellitus; Biomarkers; Differentially expressed proteins; Retinol-binding protein 4; Angiopoietin-like 8; Proteomics; Lifestyle interventions; Early prediction

Core Tip: The letter highlights certain limitations of the study by Cao et al, which explored early second-trimester biomarkers, retinol-binding protein 4 and angiopoietin-like 8, for predicting gestational diabetes mellitus (GDM). While valuable, identifying GDM in the early second trimester may not provide sufficient time for pregnant mothers to adopt major lifestyle interventions. Early first-trimester prediction or pre-conceptional identification would be more clinically significant. While the study uses advanced proteomic techniques, including isobaric tags for relative and absolute quantitation and liquid chromatography-mass spectrometry, to identify differentially expressed proteins, it is constrained by a small sample size and methodological gaps. Specifically, the reliability of protein quantification and high-abundance protein removal is unclear, and the lack of experimental validation limits the functional interpretation of identified protein interactions.