Key result
Higher baseline neuron-specific enolase is linked to ~18% greater risk of post-stroke depression.
Why the study?
Do baseline NIHSS and NSE predict the risk of post-stroke depression at 3 months in patients with acute ischemic stroke?
Cohort (n=172)
Do baseline NIHSS and NSE predict the risk of post-stroke depression at 3 months in patients with acute ischemic stroke?
Odds Ratio: 1.18 (95% CI 1.037–1.343)
p-value: p=<0.05
A nomogram incorporating sex, age, baseline NIHSS, and NSE can help predict the risk of post-stroke depression at 3 months in patients with acute ischemic stroke.
Objective The National Institutes of Health Stroke Scale (NIHSS) is a known risk factor for post-stroke depression (PSD). However, more objective indicators are needed. The role of neuron-specific enolase (NSE) in PSD development remains unclear. This study aimed to ascertain the correlation of NIHSS score and NSE with PSD risk, and establish a novel nomogram combining NSE and NIHSS for early PSD prediction.Methods A total of 172 patients with acute ischemic stroke (AIS) were involved. Baseline clinical data including NSE and NIHSS were collected. At 3-month follow-up, patients were categorized into PSD and non-PSD groups. Logistic models and restricted cubic spline curve were used to investigate the correlation between NIHSS, NSE and PSD. A corresponding nomogram was formulated.Results Among 172 patients with AIS, 63 (36.63%) were diagnosed with PSD, while 109 (63.37%) were non-PSD. The baseline NIHSS and NSE were positively correlated with the risk of 3-month PSD (P < 0.05). Multivariate logistic regression revealed that sex (OR= 2.168, 95% CI 1.038 ∼ 4.526), age (OR= 1.035, 95% CI 1.002 ∼ 1.070), NIHSS (OR= 1.164, 95% CI 1.022 ∼ 1.325) and NSE (OR= 1.180, 95% CI 1.037 ∼ 1.343) were independently associated with 3-month PSD (all P < 0.05). The nomogram constructed using sex, age, baseline NIHSS score and NSE showed good discrimination, calibration, and clinical utility.Conclusion NSE is a valuable tool for early identification of PSD risk. A combined prediction model incorporating NIHSS and NSE has been established for the personalized prevention and intervention of PSD.
No takes yet. Share an insight, caveat, or question.
Yan et al. (2025) conducted a cohort in acute ischemic stroke (AIS) (n=172). Neuron-specific enolase (NSE) and NIHSS score was evaluated on 3-month post-stroke depression (PSD) (OR 1.180, 95% CI 1.037-1.343, p=<0.05). Baseline neuron-specific enolase (OR 1.180; 95% CI 1.037-1.343) and NIHSS (OR 1.164; 95% CI 1.022-1.325) were independently associated with 3-month post-stroke depression.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: