Evidence map›Paper›PMID 41021209›Full record

ArticleJournal of endocrinological investigation2026

Potential role of insulin-like growth factor 1 and growth hormone in acneiform eruptions: evidence from a rat model of acromegaly.

Mengjie Fan, Yangfan Lai, Xiaoyao Fan, Yichang Yuan, Jin Chen, Yanzhuo Hu, Ye Liu, Min He, Meiyan Liu, Hongying Ye and 5 more

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of endocrinological investigation, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Mengjie Fan *Department of Dermatology, Huashan Hospital, Fudan University, 12 Wulumuqi Middle Road, Shanghai, 200040, People's Republic of China.
Yangfan Lai *Department of Dermatology, Huashan Hospital, Fudan University, 12 Wulumuqi Middle Road, Shanghai, 200040, People's Republic of China.
Xiaoyao Fan *Department of Dermatology, Huashan Hospital, Fudan University, 12 Wulumuqi Middle Road, Shanghai, 200040, People's Republic of China.
Yichang YuanSchool of Life Science and Technology, ShanghaiTech University, 393 Huaxia Middle Road, Shanghai, 201210, People's Republic of China.
Jin ChenDepartment of Dermatology, Huashan Hospital, Fudan University, 12 Wulumuqi Middle Road, Shanghai, 200040, People's Republic of China.
Yanzhuo HuDepartment of Dermatology, Huashan Hospital, Fudan University, 12 Wulumuqi Middle Road, Shanghai, 200040, People's Republic of China.
Ye LiuDepartment of Dermatology, Huashan Hospital, Fudan University, 12 Wulumuqi Middle Road, Shanghai, 200040, People's Republic of China.
Min HeDepartment of Endocrinology, Huashan Hospital, Fudan University, 12 Wulumuqi Middle Road, Shanghai, 200040, People's Republic of China.
Meiyan LiuDepartment of Endocrinology, Huashan Hospital, Fudan University, 12 Wulumuqi Middle Road, Shanghai, 200040, People's Republic of China.
Hongying YeDepartment of Endocrinology, Huashan Hospital, Fudan University, 12 Wulumuqi Middle Road, Shanghai, 200040, People's Republic of China.
Zhaoyun ZhangDepartment of Endocrinology, Huashan Hospital, Fudan University, 12 Wulumuqi Middle Road, Shanghai, 200040, People's Republic of China.
Yongfei WangDepartment of Neurosurgery, Huashan Hospital, Fudan University, 12 Wulumuqi Middle Road, Shanghai, 200040, People's Republic of China.
Leihong XiangDepartment of Dermatology, Huashan Hospital, Fudan University, 12 Wulumuqi Middle Road, Shanghai, 200040, People's Republic of China.
Zhengyuan ChenDepartment of Neurosurgery, Huashan Hospital, Fudan University, 12 Wulumuqi Middle Road, Shanghai, 200040, People's Republic of China. chenzy18@fudan.edu.cn.
Ying MaDepartment of Dermatology, Huashan Hospital, Fudan University, 12 Wulumuqi Middle Road, Shanghai, 200040, People's Republic of China. alle_ma@163.com.ORCID http://orcid.org/0000-0003-3688-8972

Funding

Clinical Research Plan of Shanghai Hospital Development Center SHDC22022302National Key Research and Development Program of China 2023YFC2509000National Natural Science Foundation of China 82173444National Natural Science Foundation of China 82304053
6 · The paper itself

Abstract

backgroundAcne, a chronic inflammatory disease, is influenced by insulin-like growth factor 1 (IGF-1). Acromegaly, characterized by excessive growth hormone (GH) and IGF-1, is associated with a higher prevalence of acne, though the underlying mechanisms remain unclear.

objectiveThis study aims to explore the underlying mechanisms why patients with acromegaly are more susceptible to acne, especially refractory acne.

methodsAn acromegaly rat model was established via biweekly long-acting recombinant human GH (rhGH) injections for eight weeks. Serum levels of GH, IGF-1, and glucose were measured, and skin pathology was examined. Immunohistochemistry, transcriptomics, and proteomics were performed to explore molecular pathways, with RT-qPCR and western blot validation.

resultsSerum GH and IGF-1 levels significantly increased from week 3 and remained elevated throughout the study in the rhGH-treated group. Acneiform lesions, including epidermal hyperkeratosis, sebaceous gland hyperplasia, and dermal thickening, were observed. Immunohistochemical analysis revealed upregulation of IGF-1, IGF-1R, SREBP1, and IL-1β. Transcriptomic and proteomic analyses identified 1,112 differentially expressed genes and 440 differentially expressed proteins, underscoring the activation of inflammation, extracellular matrix (ECM) remodeling, epithelial-mesenchymal transition (EMT), and cell proliferation through PI3K/Akt pathways. Significant upregulation of matrix metalloproteinases (MMPs) and tissue inhibitor of metalloproteinase 1 (TIMP-1) was observed in both transcriptomic and proteomic analyses.

conclusionChronic GH stimulation leads to persistent IGF-1 elevation, promoting acne by increasing IGF-1R expression and disrupting ECM remodeling via PI3K/Akt-regulated MMPs and TIMP-1. These findings help clarify the link between acromegaly and acne and provide mechanistic insights into the role of IGF-1 in acne pathogenesis.

Indexed as

Acneiform EruptionsAcromegalyGrowth HormoneHuman Growth HormoneInsulin-Like Growth Factor IAnimalsDisease Models, AnimalHumansMaleProteomicsRatsRats, Sprague-DawleySignal TransductionGrowth HormoneHuman Growth HormoneInsulin-Like Growth Factor IAcneAcromegalyIGF-1Muti-omicsPI3K/Akt

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.