# Development and validation of a nomogram for early prediction of post-stroke shoulder–hand syndrome: a retrospective cohort study

**Authors:** Xuezheng Li, Yu Min, Lulu Cheng, Yunyun Tao, Meifeng Zheng, Hua Guo, Xuefeng Fu, Lijun Lu, Wen Yang, Hao Li, Zhen Huang, Kaifeng Guo

PMC · DOI: 10.3389/fnins.2026.1681392 · Frontiers in Neuroscience · 2026-02-09

## TL;DR

This study creates a tool to predict shoulder-hand syndrome after stroke, using patient data to help doctors develop prevention plans.

## Contribution

The study introduces a validated nomogram for early prediction of post-stroke shoulder-hand syndrome using clinical features.

## Key findings

- The nomogram achieved an AUC of 0.777 in the training set and 0.698 in the validation set.
- Key predictors included sex, occupation, residence, and several medical conditions and lab values.
- The model can predict SHS occurrence within 6 months after stroke with reasonable accuracy.

## Abstract

Shoulder-hand syndrome (SHS) is a prevalent complication following strokes. At present, there is no established and dependable method for early prediction of SHS risk. Thus, we undertook this study to create and validate a nomogram for early prediction of SHS following ischemic stroke (IS), with the aim of informing the development of SHS-specific follow-up protocols in clinical practice.

We retrospectively collected data on IS patients admitted to the Affiliated Panyu Central Hospital of Guangzhou Medical University from October 1, 2019 to March 31, 2024. The data was randomly split into a training set and a validation set in a 7:3 ratio, and LASSO regression was used to filter the modeling variables. In addition, the consistency index, area under the receiver operating characteristic curve (AUC), and calibration curve were used to verify the accuracy and discriminant power of the nomogram.

A total of 514 patients were enrolled in our study. Significant predictors contained sex, occupation, residence, osteoarthritis, gouty arthritis, myodynamia, heart rate, neutrophils, blood glucose, aspartate aminotransferase, and activated partial thromboplastin time. The AUC for the model constructed on the basis of these predictors was 0.777 (95% CI: 0.727–0.826) in the training set and 0.698 (95% CI: 0.615–0.781) in the validation set.

The nomogram constructed on the basis of common clinical features has a high performance in predicting the occurrence of SHS within 6 months after stroke. It can provide a reference for the development of specific prevention programs during clinical practice.

## Linked entities

- **Diseases:** ischemic stroke (MONDO:1060198), osteoarthritis (MONDO:0005178)

## Full-text entities

- **Genes:** SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, PLG (plasminogen) [NCBI Gene 5340] {aka HAE4}, FGB (fibrinogen beta chain) [NCBI Gene 2244] {aka HEL-S-78p}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}
- **Diseases:** middle cerebral artery infarction (MESH:D020244), cerebral hemorrhage (MESH:D002543), biceps longus tendinitis (MESH:D052256), hematological disorders (MESH:D006402), Brain injury (MESH:D001930), hypertension (MESH:D006973), obstruction of venous return (MESH:D012587), osteoporosis (MESH:D010024), ACS (MESH:D000168), urinary tract infection (MESH:D014552), circulation (MESH:D009360), cerebrovascular disease (MESH:D002561), IS (MESH:D002544), immune system disorders (MESH:D007154), blood coagulation (MESH:D001778), myocardial infarction (MESH:D009203), hemiplegia (MESH:D006429), coronary artery disease (MESH:D003324), hyperhomocysteinemia (MESH:D020138), depression (MESH:D003866), dyskinesia (MESH:D004409), HF (MESH:D006333), TIA (MESH:D002546), degeneration and (MESH:D009410), impaired motor function (MESH:D000068079), hyperuricemia (MESH:D033461), joint subluxation (MESH:D004204), coronary heart disease (MESH:D003327), compression neuropathy (MESH:D009408), acute coronary syndrome (MESH:D054058), brachial plexus injury (MESH:D020516), Pain (MESH:D010146), hyperlipidemia (MESH:D006949), hepatic or renal insufficiency (MESH:D048550), abnormalities in the nervous system (MESH:D009421), muscle atrophy (MESH:D009133), Inflammatory (MESH:D007249), spasticity (MESH:D009128), infection of the lungs (MESH:D012141), trauma (MESH:D014947), HL (MESH:C538324), adhesion bursitis (MESH:D002062), edema (MESH:D004487), central nervous system damage (MESH:D002493), GA (MESH:D015210), traumatic brain injury (MESH:D000070642), neoplasms (MESH:D009369), HSP (MESH:D020069), diabetes (MESH:D003920), sensory disturbance (MESH:D012678), Stroke (MESH:D020521), protein-energy malnutrition (MESH:D011502), Hypercoagulation (MESH:D019851), Loss of motor function (MESH:D003291), paralysis (MESH:D010243), wear of articular cartilage (MESH:D002357), CRPS (MESH:D020918), fever (MESH:D005334), shoulder abductor myodynamia (MESH:D000070599), CRPS-I (MESH:D012019)
- **Chemicals:** Na+ (MESH:D012964), K+ (MESH:D011188), HCY (MESH:D006710), urea nitrogen (MESH:C530477), creatinine (MESH:D003404), GLU (MESH:D005947), alcohol (MESH:D000438), UA (MESH:D014527), blood glucose (MESH:D001786)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## References

44 references — full list in the complete paper: https://tomesphere.com/paper/PMC12926463/full.md

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Source: https://tomesphere.com/paper/PMC12926463