# Proteomic signatures of intermittent pneumatic compression in patients with large artery atherosclerotic stroke

**Authors:** Shasha Lei, Zhenzhen Wang, Dandang Ouyang, Tingjing Huang, Kaili Huang, Xinying Li, Zhi-Xin Huang

PMC · DOI: 10.1016/j.isci.2026.114915 · iScience · 2026-02-10

## TL;DR

This study finds that intermittent pneumatic compression affects specific proteins in stroke patients, possibly influencing recovery pathways.

## Contribution

The study identifies 12 proteins modulated by IPC in stroke patients, linking them to neurological outcomes and vascular risk.

## Key findings

- IPC modulates 12 proteins, 93.3% of which increase after intervention.
- ANGPT1 and SOD2 are key proteins linked to angiogenesis, antioxidant, and inflammation pathways.
- Protein changes correlate with NIHSS and ESRS scores, suggesting a role in stroke recovery.

## Abstract

Intermittent pneumatic compression (IPC) is routinely used after stroke for venous thromboembolism prophylaxis, yet its molecular mechanisms remain elusive. In a single-blind randomized pilot trial, 44 patients with large-artery atherosclerotic ischemic stroke were assigned to bilateral IPC twice daily (n = 22) or unilateral compression once daily (n = 22) for 7 (SD = 2) days. Cardiovascular proteins were quantified with the Olink platform, and treatment-specific changes were identified using a prespecified triple orthogonal screening strategy. IPC was associated with 12 treatment-specific proteins, 93.3% of which increased after intervention. ANGPT1 and SOD2 were prominent candidates, mapping to angiogenesis, antioxidant, and inflammation pathways, including Ras signaling, correlating with NIHSS and ESRS scores. These hypothesis-generating data suggest IPC modulates defined protein networks (Ras-ANGPT1-related and SOD2-mediated antioxidant pathways) that may support mechanistic and precision rehabilitation studies, pending validation in larger cohorts.

•Ischemic preconditioning (IPC) alters levels of 12 circulating proteins in patients with stroke•IPC-induced protein changes correlate with neurological outcomes and vascular risk scores•IPC modulates proteins in oxidative stress, inflammation, and vascular remodeling pathways•Angiopoietin-1 (angiogenic) and SOD2 (antioxidant) emerge as key proteins upregulated by IPC

Ischemic preconditioning (IPC) alters levels of 12 circulating proteins in patients with stroke

IPC-induced protein changes correlate with neurological outcomes and vascular risk scores

IPC modulates proteins in oxidative stress, inflammation, and vascular remodeling pathways

Angiopoietin-1 (angiogenic) and SOD2 (antioxidant) emerge as key proteins upregulated by IPC

Health sciences; Medicine; Medical specialty; Cardiovascular medicine

## Linked entities

- **Proteins:** ANGPT1 (angiopoietin 1), SOD2 (superoxide dismutase 2)
- **Diseases:** ischemic stroke (MONDO:1060198)

## Full-text entities

- **Genes:** DECR1 (2,4-dienoyl-CoA reductase 1) [NCBI Gene 1666] {aka DECR, NADPH, SDR18C1}, HBEGF (heparin binding EGF like growth factor) [NCBI Gene 1839] {aka DTR, DTS, DTSF, HEGFL}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, OLR1 (oxidized low density lipoprotein receptor 1) [NCBI Gene 4973] {aka CLEC8A, LOX1, LOXIN, SCARE1, SLOX1}, MARCO (macrophage receptor with collagenous structure) [NCBI Gene 8685] {aka SCARA2, SR-A6}, IKBKG (inhibitor of nuclear factor kappa B kinase regulatory subunit gamma) [NCBI Gene 8517] {aka AMCBX1, EDAID1, FIP-3, FIP3, Fip3p, IKK-gamma}, CD40LG (CD40 ligand) [NCBI Gene 959] {aka CD154, CD40L, HIGM1, IGM, IMD3, T-BAM}, SOD2 (superoxide dismutase 2) [NCBI Gene 6648] {aka GC1, GClnc1, IPO-B, IPOB, MNSOD, MVCD6}, SPON2 (spondin 2) [NCBI Gene 10417] {aka DIL-1, DIL1, M-SPONDIN, MINDIN}, ANGPT1 (angiopoietin 1) [NCBI Gene 284] {aka AGP1, AGPT, AGPT-1, ANG1, HAE5}, HAO1 (hydroxyacid oxidase 1) [NCBI Gene 54363] {aka GO, GOX, GOX1, HAOX1}, SORT1 (sortilin 1) [NCBI Gene 6272] {aka Gp95, LDLCQ6, NT3, NTR3}, EGF (epidermal growth factor) [NCBI Gene 1950] {aka HOMG4, URG}
- **Diseases:** inflammation (MESH:D007249), death (MESH:D003643), NIHSS (MESH:C538175), immunodeficiency (MESH:D007153), VTE (MESH:D054556), stenosis or occlusion of major cerebral arteries (MESH:D001157), IPC (MESH:D009408), atherosclerosis (MESH:D050197), ischemic brain damage (MESH:D001925), infection (MESH:D007239), ischemic stroke (MESH:D002544), ischemic (MESH:D002545), ischemic disease (MESH:D017202), post (MESH:D000094025), deep vein thrombosis (MESH:D020246), neuroinflammation (MESH:D000090862), ulcers (MESH:D014456), deformity (MESH:D009140), neuronal death (MESH:D009410), hemorrhagic transformation (MESH:D006470), congestive heart failure (MESH:D006333), infarct (MESH:D007238), dermatitis (MESH:D003872), allergic reactions (MESH:D004342), atherosclerotic stroke (MESH:D002537), Stroke (MESH:D020521), micro (MESH:C536681), ischemia (MESH:D007511), Neurological deficit (MESH:D009461), thrombophlebitis (MESH:D013924), LAA stroke (MESH:D020243), venous stasis (MESH:D054070), disability (MESH:D009069), neurological impairment (MESH:D009422), skin abnormalities (MESH:D012868)
- **Chemicals:** KY-KZ-239-03 (-), EDTA (MESH:D004492), lipid (MESH:D008055), cholesterol (MESH:D002784), reactive oxygen species (MESH:D017382)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12936827/full.md

## References

27 references — full list in the complete paper: https://tomesphere.com/paper/PMC12936827/full.md

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Source: https://tomesphere.com/paper/PMC12936827