Evidence map›Paper›PMID 40179941›Full record

ReviewRenal failure2025

High altitude renal syndrome: four elements or one source?

Lei Zhang, Erchao Feng, Sezhen Baima, Cangjue Laba, Lazhen Suolang, Ji Cang, Qing De

Abstract readReview
In one paragraph

Review in Renal failure, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
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

7 authors.

Lei ZhangThe First Affiliated Hospital of Anhui University of Chinese Medicine, Hefei, Anhui Province, China.ORCID 0009-0005-9012-9952
Erchao FengCenter for High Altitude Disease Diagnosis and Treatment/Renal Department, Shannan People's Hospital Shannan City Tibet Autonomous Region, China.
Sezhen BaimaCenter for High Altitude Disease Diagnosis and Treatment/Renal Department, Shannan People's Hospital Shannan City Tibet Autonomous Region, China.
Cangjue LabaCenter for High Altitude Disease Diagnosis and Treatment/Renal Department, Shannan People's Hospital Shannan City Tibet Autonomous Region, China.
Lazhen SuolangCenter for High Altitude Disease Diagnosis and Treatment/Renal Department, Shannan People's Hospital Shannan City Tibet Autonomous Region, China.
Ji CangCenter for High Altitude Disease Diagnosis and Treatment/Renal Department, Shannan People's Hospital Shannan City Tibet Autonomous Region, China.
Qing DeCenter for High Altitude Disease Diagnosis and Treatment/Renal Department, Shannan People's Hospital Shannan City Tibet Autonomous Region, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High Altitude Renal Syndrome (HARS) is a clinical syndrome characterized by polycythemia, hyperuricemia, hypertension, and albuminuria at high altitudes. This review emphasizes hypoxia-induced High Altitude Polycythemia (HAPC) as its core driver. In 2014, the 6th Qinghai International Conference on Mountain Medicine and High Altitude Physiology established international diagnostic criteria for HAPC (hemoglobin ≥210g/L in males, ≥190g/L in females). HAPC triggers systemic hypoxia, leading to hyperuricemia via uric acid overproduction and reduced renal excretion, hypertension from hemodynamic changes, and glomerular injury through erythrocytosis. Pathological mechanisms involve HIF-2α-mediated glomerular hypertrophy and podocyte damage. Treatment strategies target HAPC and downstream effects. Carbonic anhydrase inhibitors (e.g., acetazolamide) reduce hematocrit and improve oxygen saturation, but newer agents like methazolamide and dichlorphenamide offer equivalent efficacy with fewer side effects (e.g., reduced central nervous system toxicity). For severe cases, descending to lower altitudes remains the gold standard. Additional interventions include calcium channel blockers (nifedipine), urate-lowering drugs, and experimental therapies such as HIF-2α inhibitors (PT2385) and endothelin receptor antagonists (matitan). This analysis underscores HAPC as the primary etiology of HARS, advocating revised diagnostic criteria and treatment prioritization.

Indexed as

Altitude SicknessPolycythemiaAlbuminuriaAltitudeCalcium Channel BlockersCarbonic Anhydrase InhibitorsHumansHypertensionHyperuricemiaHypoxiaCalcium Channel BlockersCarbonic Anhydrase Inhibitorsaltitude descentcarbonic anhydrase inhibitorshigh altitude polycythemiaHigh altitude renal syndromehypoxiapathogenesis

Identifiers

PMID40179941
PMCPMC11983532

What OpenQuestion holds

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Registered trials

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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.