Single nucleus RNA sequencing reveals testosterone replacement therapy-associated multicellular remodelling of skeletal muscle in hypogonadal men with Klinefelter Syndrome

Clicks: 5
ID: 317765
2026
Article Quality & Performance Metrics
Overall Quality
Not rated
Combines reader engagement with the AI quality analysis. This article has not been analysed, so there is no overall score — reader engagement is measured and shown alongside.
AI Quality Assessment
Not analyzed
Readership in this journal
Steady

Ranked #163 of 367 articles by views in the journal of clinical endocrinology & metabolism

Most read Least read

Bar heights use a square-root scale. Only the 120 most-read articles are drawn; the journal has 367 in total.

Mint this article as an NFT
Not yet minted

Create a permanent, verifiable on-chain record of this article on the Scimatic Network. The NFT is held in your Journament account, and you can withdraw it to your own wallet at any time.

5 SUSD one-off · no wallet required
Abstract
BACKGROUND: Klinefelter syndrome (KS) is characterized by hypogonadism, resulting in metabolic disturbances and altered body composition, including reduced muscle mass. Although testosterone replacement therapy (TRT) is a standard treatment, its effects on skeletal muscle remain incompletely understood. METHODS: Single-nucleus RNA-sequencing was applied to vastus lateralis biopsies from patients with KS (n = 4), collected at the time of diagnosis and again after one year of TRT. Reference material was retrieved from age-matched male controls (n = 4). We profiled nuclear transcriptomes across ten cell types residing within the skeletal muscle. RESULTS: At diagnosis, sex hormone measurements confirmed hypogonadism in the untreated KS group. One year of TRT effectively normalized serum testosterone and reduced LH and FSH levels. Furthermore, three in four KS patients gained muscle mass.We obtained transcriptomic data from 81,786 individual nuclei. At baseline, untreated KS muscle exhibited pervasive transcriptional reprogramming with indications of changes to myogenic differentiation and heightened fibrotic, adipogenic, and inflammatory transcriptomic profiles. Pseudotime trajectory analysis indicated altered progression from muscle stem to progenitor states. After TRT, gene expression shifted toward gene-patterns linked to improved structural integrity, regeneration, and vascular remodelling. Nevertheless, a substantial KS-specific signature persisted including increased inflammatory signalling. CONCLUSION: In this exploratory pilot study, TRT was associated with a shift toward a more pro-regenerative skeletal muscle transcriptional environment in patients with KS, though only partially mitigating some of the adverse effects of long-standing hypogonadism and KS.
Reference Key
openalex_W7165031500 Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Emma B. Johannsen, Lukas Ochsner Reynaud Ridder, Agnete Nørgaard Schou, Jakob Wang, Jean Farup, Lin Lin, Jesper Just, Claus Højbjerg Gravholt
Journal the journal of clinical endocrinology & metabolism
Year 2026
DOI
10.1210/clinem/dgag240
URL
Keywords Keywords not found

Citations

No citations found. To add a citation, contact the admin at info@scimatic.org

No comments yet. Be the first to comment on this article.