ReviewCureus2025
Pulmonary Hypertension in Systemic Lupus Erythematosus: Current Evidence and Future Directions.
Review in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
- Research advances in connective tissue disease-associated pulmonary arterial hypertension with an emphasis on the Chinese population.Frontiers in medicine · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Pulmonary hypertension (PH) is an uncommon but serious manifestation of systemic lupus erythematosus (SLE) that significantly impacts prognosis. Its subtle clinical presentation often overlaps with other cardiopulmonary complications, leading to underdiagnosis and delayed treatment. Immune-mediated endothelial injury, chronic inflammation, and progressive vascular remodeling contribute to increased pulmonary arterial pressure and right ventricular dysfunction. Advances in molecular and immunologic research have identified distinct biological profiles in SLE-associated PH, highlighting the roles of endothelial dysfunction, cytokine imbalance, and specific autoantibodies in disease progression. These insights support precision medicine approaches targeting both immune and vascular pathways. Early recognition and multidisciplinary management are essential, with echocardiography and right heart catheterization remaining fundamental for diagnosis, and biomarkers aiding in risk stratification. Treatment typically combines immunosuppressive and pulmonary vasodilator therapies, with corticosteroids and cyclophosphamide as first-line options, while biologic agents and targeted vasodilator combinations may further enhance clinical outcomes. SLE-associated PH exemplifies the intersection of autoimmunity and vascular disease, and integrating novel diagnostic and therapeutic strategies may improve early detection and survival outcomes.
Indexed as
Identifiers
What Socratic holds
Registered trials
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 Socratic graph.