Evidence map›Paper›PMID 41718952›Full record

ReviewCurrent atherosclerosis reports2026

Surfactant Protein B and the Lung-HDL-Vascular Axis: Linking Pulmonary Injury to Cardiovascular Risk.

Baohai Shao

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current atherosclerosis reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

1 author.

Baohai ShaoDepartment of Medicine, University of Washington, Box 358062, 850 Republican Street, Seattle, WA, 98109, United States. bhshao@uw.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purpose of reviewPulmonary surfactant protein B (SFTPB) is a lung-specific protein essential for surfactant function. This review summarizes its biology, circulation during pulmonary injury, association with high-density lipoprotein (HDL), and emerging links to cardiovascular disease (CVD). RECENT

findingsAlveolar–capillary barrier disruption in heart failure, valvular disease, acute respiratory distress syndrome, and smoking permits immature SFTPB (pro-SFTPB) to enter the bloodstream. Circulating pro-SFTPB binds predominantly to HDL, impairing antioxidant capacity while largely preserving cholesterol efflux and endothelial anti-inflammatory functions. HDL-bound SFTPB reflects pulmonary–vascular stress and predicts incident CVD independently of traditional risk factors. These observations support a “lung–HDL–vascular” axis in which alveolar–capillary injury is encoded in circulating HDL. SFTPB functions as a sensitive biomarker of lung–vascular crosstalk, and future studies should clarify its functional relevance, temporal dynamics, and translational potential.

Indexed as

Cardiovascular DiseasesLipoproteins, HDLLungLung InjuryPulmonary Surfactant-Associated Protein BAnimalsBiomarkersHeart Disease Risk FactorsHumansRisk FactorsBiomarkersLipoproteins, HDLPulmonary Surfactant-Associated Protein BAlveolar–capillary barrier disruptionCardiovascular diseaseHDL proteomicsHeart failureHigh-density lipoproteinSurfactant protein B

Identifiers

What OpenQuestion holds

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Registered trials

None linked

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.