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11/14/2025 8:23:13 AM | Browse: 21 | Download: 130
Publication Name World Journal of Diabetes
Manuscript ID 112236
Country China
Received
2025-07-22 03:31
Peer-Review Started
2025-07-24 00:11
First Decision by Editorial Office Director
2025-08-06 11:08
Return for Revision
2025-08-06 11:08
Revised
2025-08-06 16:46
Publication Fee Transferred
Second Decision by Editor
2025-09-08 00:16
Second Decision by Editor-in-Chief
Final Decision by Editorial Office Director
2025-09-22 05:23
Articles in Press
2025-09-22 05:23
Edit the Manuscript by Language Editor
Typeset the Manuscript
2025-10-24 08:27
Publish the Manuscript Online
2025-11-14 08:23
ISSN 1948-9358 (online)
Open Access This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/Licenses/by-nc/4.0/
Copyright © The Author(s) 2025. Published by Baishideng Publishing Group Inc. All rights reserved.
Article Reprints For details, please visit: http://www.wjgnet.com/bpg/gerinfo/247
Permissions For details, please visit: http://www.wjgnet.com/bpg/gerinfo/207
Publisher Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
Website http://www.wjgnet.com
Category Endocrinology & Metabolism
Manuscript Type Review
Article Title Androgen receptor mutations in familial androgen insensitivity syndrome: A metabolic reprogramming pathway to type 2 diabetes susceptibility
Manuscript Source Invited Manuscript
All Author List Cheng Luo, Wei-Wei Zhang, Liang-Yan Hua, Mei-Qi Zeng, Hui Xu, Cheng-Zheng Duan, Shi-Yu Xu, Shuo Zhan, Xiao-Fei Pan, Da Sun, Li-Ya Ye and Dong-Juan He
ORCID
Author(s) ORCID Number
Cheng Luo http://orcid.org/0009-0008-2257-6066
Wei-Wei Zhang http://orcid.org/0009-0000-9360-0686
Liang-Yan Hua http://orcid.org/0009-0002-1156-7638
Mei-Qi Zeng http://orcid.org/0009-0000-5376-5021
Hui Xu http://orcid.org/0009-0004-6817-1954
Cheng-Zheng Duan http://orcid.org/0009-0002-4768-6911
Shi-Yu Xu http://orcid.org/0009-0003-5450-9670
Shuo Zhan http://orcid.org/0009-0009-3147-3779
Xiao-Fei Pan http://orcid.org/0009-0002-4234-4584
Da Sun http://orcid.org/0000-0001-7747-9951
Li-Ya Ye http://orcid.org/0009-0001-6288-7933
Dong-Juan He http://orcid.org/0009-0001-1750-127X
Funding Agency and Grant Number
Funding Agency Grant Number
Quzhou Science and Technology Plan Project No. 2022K69
Corresponding Author Dong-Juan He, Chief Physician, Dean, Director, Professor, Department of Endocrinology, The Second People’s Hospital of Quzhou, No. 338 Xin’an Avenue, Qujiang District, Quzhou 324002, Zhejiang Province, China. hedongjuan1247@wmu.edu.cn
Key Words Androgen insensitivity syndrome; Androgen receptor; Gene mutation; Metabolic reprogramming; Type 2 diabetes
Core Tip Familial androgen insensitivity syndrome (AIS), caused by androgen receptor gene mutations, has long been viewed as a disorder of sex development. However, recent findings revealed that androgen receptor dysfunction also drives metabolic reprogramming in key tissues - pancreatic β-cells, skeletal muscle, liver, and adipose tissue - leading to insulin resistance and increased susceptibility to type 2 diabetes mellitus. This article highlights emerging evidence of glucagon-like peptide-1 signaling disruption, mitochondrial dysfunction, and inflammatory imbalance in AIS. We propose an integrated framework of genetic screening, endocrine surveillance, and individualized therapy to improve long-term metabolic outcomes and prevent cardiometabolic complications in AIS patients.
Publish Date 2025-11-14 08:23
Citation

Luo C, Zhang WW, Hua LY, Zeng MQ, Xu H, Duan CZ, Xu SY, Zhan S, Pan XF, Sun D, Ye LY, He DJ. Androgen receptor mutations in familial androgen insensitivity syndrome: A metabolic reprogramming pathway to type 2 diabetes susceptibility. World J Diabetes 2025; 16(11): 112236

URL https://www.wjgnet.com/1948-9358/full/v16/i11/112236.htm
DOI https://dx.doi.org/10.4239/wjd.v16.i11.112236
Full Article (PDF) WJD-16-112236-with-cover.pdf
Manuscript File 112236_Auto_Edited_095335.docx
Answering Reviewers 112236-answering-reviewers.pdf
Audio Core Tip 112236-audio.mp3
Conflict-of-Interest Disclosure Form 112236-conflict-of-interest-statement.pdf
Copyright License Agreement 112236-copyright-assignment.pdf
Non-Native Speakers of English Editing Certificate 112236-non-native-speakers.pdf
Peer-review Report 112236-peer-reviews.pdf
Scientific Misconduct Check 112236-scientific-misconduct-check.png
Scientific Editor Work List 112236-scientific-editor-work-list.pdf
CrossCheck Report 112236-crosscheck-report.pdf