# Tea consumption is associated with a reduced risk of high-altitude pulmonary hypertension among high-altitude permanent inhabitants in the Tibetan population: a case-control study

**Authors:** Wuyang Tong, Ran Cheng, Xiaoming Chen, Xuesen Zhang, Wanmin Li, Xiaqing Luo, Shipeng Xu, Xianjin Bi

PMC · DOI: 10.3389/fnut.2026.1732242 · Frontiers in Nutrition · 2026-02-10

## TL;DR

Drinking tea, especially Tibetan tea, is linked to a lower risk of high-altitude pulmonary hypertension in Tibetans living at high altitudes.

## Contribution

This study identifies tea consumption as a novel protective factor against high-altitude pulmonary hypertension in a Tibetan population.

## Key findings

- HAPH patients consumed tea less frequently than controls (45.1% vs. 59.3%).
- Tibetan tea showed the strongest protective effect against HAPH (adjusted OR = 0.300).
- Higher tea consumption frequency, quantity, and duration were associated with reduced HAPH risk.

## Abstract

This study investigated the potential association between tea consumption and high-altitude pulmonary hypertension (HAPH) risk in a long-term, high-altitude Tibetan population, which remained unexplored.

In a hospital-based case-control study, 113 patients with HAPH and 113 controls were included. Data were collected from medical records and a tea consumption questionnaire. Group comparisons were performed using t-tests, Mann–Whitney U, Chi-square, or Fisher's exact test. Univariate and multivariable logistic regression analyses determined the tea–HAPH relationship (p < 0.05).

Patients with HAPH exhibited significant right-heart structural alterations and a distinct metabolic profile characterized by lower lipid and glucose levels. A significant inverse association was observed between tea consumption and HAPH risk. Compared to the control group, patients with HAPH exhibited a significantly lower proportion of tea consumption (45.1% vs. 59.3%, p = 0.033). After adjusting for confounders, including age, hemodynamic, and metabolic parameters, regular tea consumption remained an independent protective factor (adjusted OR = 0.496, 95% CI: 0.258–0.952). Tibetan tea exhibited the strongest protective effect (adjusted OR = 0.300, 95% CI: 0.123–0.735). A significant dose-response relationship was observed, with the significant risk reduction at higher consumption frequency (≥6 days/week: adjusted OR = 0.208), more tea consumption (≥3 cups/day: adjusted OR = 0.305), and longer duration (≥20 years: adjusted OR = 0.210).

Regular Tibetan tea consumption significantly reduces HAPH risk in a dose-response manner. These findings offer new insights into dietary factors in HAPH etiology and can explain Tibetan adaptation to high altitudes.

## Full-text entities

- **Genes:** CMPK1 (cytidine/uridine monophosphate kinase 1) [NCBI Gene 51727] {aka CK, CMK, CMPK, UMK, UMP-CMPK, UMPK}, EDN1 (endothelin 1) [NCBI Gene 1906] {aka ARCND3, ET1, HDLCQ7, PPET1, QME}
- **Diseases:** cancer (MESH:D009369), HAPH (MESH:C535833), diabetes (MESH:D003920), cardiovascular, cerebrovascular, metabolic diseases (MESH:D002318), sPAP (MESH:D000071079), inflammation (MESH:D007249), hypertension (MESH:D006973), cardiorespiratory or sleep disorders (MESH:D012893), hypoxia (MESH:D000860), PH (MESH:D006976), obesity (MESH:D009765), amyloid (MESH:C000718787)
- **Chemicals:** amino acids (MESH:D000596), UA (MESH:D014527), polysaccharides (MESH:D011134), TG (MESH:D014280), Epigallocatechin-3-gallate (MESH:C045651), TC (-), sugar (MESH:D000073893), prostacyclin (MESH:D011464), alkaloids (MESH:D000470), epigallocatechin (MESH:C057580), alcohol (MESH:D000438), epicatechin gallate (MESH:C062669), glyceride (MESH:D005989), cholesterol (MESH:D002784), nitric oxide (MESH:D009569), Glu (MESH:D005947), theabrownins (MESH:C569455), polyphenol (MESH:D059808), catechin (MESH:D002392), thromboxane A2 (MESH:D013928), lipid (MESH:D008055)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606], Camellia sinensis (black tea, species) [taxon 4442]

## Full text

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## Figures

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## References

34 references — full list in the complete paper: https://tomesphere.com/paper/PMC12929138/full.md

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Source: https://tomesphere.com/paper/PMC12929138