High Altitude and Hypoxia Open access Peer reviewed

Altitude-associated circulating biomarker profiles in native Tibetans with and without chronic mountain sickness

Yutian Zhang, Xiaoou Li, Tao Wang, Lian Liu and 6 more

Travel Medicine and Infectious Disease | Oct 17, 2026

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Rising altitude drives distinct biomarker profiles in healthy Tibetans, with CXCL8/IFN-γ/FGF/VEGF/CXCL4/TPO exhibiting an inverted U-shaped response peaking at 4,750m, and isolated MMP-3 elevation at 5,373m, indicating a transition from adaptive angiogenesis to pathological tissue remodeling at extreme-high altitude.

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AIM: Native Tibetans have adapted to chronic hypoxia, yet remain susceptible to Chronic Mountain Sickness (CMS), including high-altitude polycythemia (HAPC) and high-altitude pulmonary hypertension (HAPH). CMS prevalence rises with altitude, but mechanisms remain unclear. We aim to investigate biomarker profiles in native Tibetans with and without CMS across altitudes, including extreme altitude >5,000m. METHODS: We enrolled 91 native Tibetans across 4 altitudes (500m/3,680m/4,750m/5,373m), categorized into healthy, HAPC and HAPH groups. Seventeen biomarkers were quantified via Luminex. Biomarker associations with altitude and disease were analyzed using linear regression with Type-III-F-tests, followed by post-hoc comparison and effect-size analysis. RESULTS: Among healthy Tibetans, multiple biomarkers exhibited non-linear altitude-dependent changes. C-X-C motif chemokine ligand 8 (CXCL8), interferon-γ (IFN-γ), fibroblast growth factor (FGF), vascular endothelial growth factor (VEGF), C-X-C motif chemokine ligand 4 (CXCL4) and thrombopoietin (TPO) peaked at 4,750m and declined at 5,373m, whereas matrix metalloproteinase-3 (MMP-3) increased at 5,373m. Among plateau-dwelling Tibetans (including HAPC and HAPH), no independent main disease-status effects were detected across biomarkers. However, an altitude-disease interaction was observed for angiogenin, with reduction at 5373m in HAPH, but not in HAPC. CONCLUSION: Rising altitude drives distinct biomarker profiles in healthy Tibetans, with CXCL8/IFN-γ/FGF/VEGF/CXCL4/TPO exhibiting an inverted U-shaped response peaking at 4,750m, and isolated MMP-3 elevation at 5,373m, indicating a transition from adaptive angiogenesis to pathological tissue remodeling at extreme-high altitude. The altitude-dependent angiogenin reduction observed exclusively in HAPH at extreme altitude, indicating a dysregulated vascular reparative signaling in Tibetans with HAPH. These findings provide new insights into CMS pathogenesis across hypoxic gradient.

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Authors

Researchers on this paper

Yutian Zhang

first | Sichuan University

Xiaoou Li

middle | Sichuan University

Tao Wang

middle | Sichuan University

Lian Liu

middle | Sichuan University

Bi Ran

middle | Sichuan University

Kangzhuo Baima

middle | Xizang Minzu University | ORCID 0009-0002-5576-9565

Yue Liao

middle | Sichuan University

Fuqiang Wen

middle | Sichuan University

Jun Chen

middle | Sichuan University | ORCID 0000-0002-1571-428X

Chen Lei

last | Sichuan University

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BibTeX

@article{Zhang2026Altitude,
  title = {Altitude-associated circulating biomarker profiles in native Tibetans with and without chronic mountain sickness},
  author = {Yutian Zhang and Xiaoou Li and Tao Wang and Lian Liu and Bi Ran and Kangzhuo Baima and Yue Liao and Fuqiang Wen and Jun Chen and Chen Lei},
  journal = {Travel Medicine and Infectious Disease},
  year = {2026},
  doi = {10.1016/j.tmaid.2026.103030},
  url = {https://doi.org/10.1016/j.tmaid.2026.103030}
}

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