Department of Rehabilitation, Zhejiang Chinese Medical University Affiliated Wenzhou Hospital of Traditional Chinese Medicine, Wenzhou, Zhejiang, China.
BMC Geriatr. 2023 Mar 27;23(1):173. doi: 10.1186/s12877-023-03919-w.
Malnutrition is a common complication after stroke and may worsen neurological outcomes for patients. There are still no uniform tools for screening nutritional status for the patients with stroke. We aimed to explore the relationship between the baseline geriatric nutritional risk index (GNRI) and neurological function at the convalescence stage for patients with stroke and assessed the predictive value of the GNRI for adverse neurological outcomes.
A total of 311 patients with stroke were enrolled retrospectively. Basic information and laboratory results on admission since onset of stroke were collected. The GNRI on admission was calculated and neurological outcomes evaluated by the Barthel index at 1 month after the onset of stroke. Statistical analyses, including correlation coefficient tests, multivariate regression analyses, and receiver operating characteristic (ROC) analyses, were applied in this study.
Compared with the good outcome group, the poor outcome group showed a significantly lower GNRI on admission (P < 0.05). GNRI was associated with Barthel index (r = 0.702, P < 0.01). The GNRI was independently correlated with the Barthel index (Standardization β = 0.721, P < 0.01) and poor outcome 0.885 (95% CIs, 0.855-0.917, P < 0.01) after adjusting for covariates. Compared with no nutritional risk grades (Q4), the OR of GNRI to poor neurological outcome increased across increasing nutritional risk grades of GNRI (OR = 2.803, 95% CIs = 1.330-5.909 in Q3, 7.992, 95% CIs = 3.294-19.387 in Q2 and 14.011, 95% CIs = 3.972-49.426 in Q1, respectively, P for trend < 0.001). The area under ROC curves (AUC) of the GNRI was 0.804, which was larger than that of the NIHSS, BMI, or Albumin (P < 0.01), with an optimal cut-off value of 97.69, sensitivity of 69.51% and specificity of 77.27%. Combined GNRI with NIHSS gained the largest AUC among all the variables (all P < 0.05), with an AUC of 0.855, sensitivity of 84.75 and specificity of 72.73%.
For patients with stroke, higher nutritional risk grades at baseline indicated worse neurological function at the convalescence stage. Compared with NIHSS, BMI, and Albumin, GNRI was a competitive indicator for the risk of poor neurological outcome. The predictive property of GNRI for adverse neurological outcomes might be more powerful when combined with NIHSS.
营养不良是中风后的常见并发症,可能使患者的神经功能恶化。目前仍然没有用于筛选中风患者营养状况的统一工具。我们旨在探讨中风患者入院时的基本老年营养风险指数(GNRI)与恢复期神经功能之间的关系,并评估 GNRI 对不良神经结局的预测价值。
回顾性纳入 311 例中风患者。收集中风发病以来的基本信息和实验室结果。计算入院时的 GNRI,并在中风发病后 1 个月用巴氏指数评估神经功能结局。本研究应用相关系数检验、多元回归分析和受试者工作特征(ROC)分析等统计学分析方法。
与良好结局组相比,不良结局组入院时 GNRI 明显较低(P<0.05)。GNRI 与巴氏指数呈正相关(r=0.702,P<0.01)。GNRI 与巴氏指数独立相关(标准化β=0.721,P<0.01),与不良结局的相关性为 0.885(95%CI:0.855-0.917,P<0.01),校正协变量后。与无营养风险等级(Q4)相比,GNRI 对不良神经结局的比值比(OR)随着 GNRI 营养风险等级的升高而增加(OR=2.803,95%CI:Q3 为 1.330-5.909,Q2 为 7.992,95%CI:3.294-19.387,Q1 为 14.011,95%CI:3.972-49.426,P 趋势<0.001)。GNRI 的 ROC 曲线下面积(AUC)为 0.804,大于 NIHSS、BMI 或白蛋白的 AUC(P<0.01),最佳截断值为 97.69,灵敏度为 69.51%,特异性为 77.27%。与 NIHSS 联合 GNRI 时,所有变量的 AUC 最大(均 P<0.05),AUC 为 0.855,灵敏度为 84.75%,特异性为 72.73%。
对于中风患者,入院时较高的营养风险等级预示着恢复期神经功能较差。与 NIHSS、BMI 和白蛋白相比,GNRI 是不良神经结局风险的一个有竞争力的指标。当与 NIHSS 联合使用时,GNRI 对不良神经结局的预测性能可能更强。