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早期特发性帕金森病患者血清胰岛素样生长因子 1 水平升高。

Increased serum insulin-like growth factor 1 in early idiopathic Parkinson's disease.

机构信息

Hertie Institute for Clinical Brain Research, Department of Neurodegeneration, Hoppe-Seyler-Str 3, D-72076 Tübingen, Germany.

出版信息

J Neurol Neurosurg Psychiatry. 2010 May;81(5):536-8. doi: 10.1136/jnnp.2009.175752. Epub 2010 Feb 22.

Abstract

OBJECTIVE

Insulin-like growth factor 1 (IGF-1) provides protection against loss of dopaminergic neurons in animal models of Parkinson's disease (PD). The aim of this study was to measure serum IGF-1 in patients with PD and assess its correlation with the clinical presentation.

METHODS

Serum IGF-1 and growth hormone (GH) levels were measured in 12 patients with idiopathic PD and 12 matched healthy controls, three times over a period of 6 months after overnight fasting. Based on the results, serum IGF-1 was measured in six additional, yet untreated, PD patients.

RESULTS

IGF-1 values were stable over the whole period (r=0.83-0.93) in patients and controls. IGF-1 was significantly higher in treated PD patients than in controls at all time points (all p<0.001). There were no significant differences in serum GH levels between patients and controls. Receiver operating characteristics showed a cut-off at 114 ng/ml for differentiation of treated patients and controls (area under the curve=0.90). In the patient group, higher serum IGF-1 levels were correlated with shorter disease duration (r=-0.56, p=0.001). In the healthy control group, higher IGF-1 was correlated with slightly impaired motor performance, as measured by the Unified Parkinson's Disease Rating Scale motor score (r=0.46, p=0.005). In the untreated patient group, serum IGF-1 levels were significantly higher than in healthy controls (p<0.001). Applying the cut-off value of 114 ng/ml, all untreated patients were correctly classified as PD patients.

CONCLUSION

Increased IGF-1 might be an interesting serum marker for early PD and potentially for subclinical dopaminergic dysfunction.

摘要

目的

胰岛素样生长因子 1(IGF-1)可提供对帕金森病(PD)动物模型中多巴胺能神经元丢失的保护作用。本研究旨在测量 PD 患者的血清 IGF-1 并评估其与临床表现的相关性。

方法

在 12 名特发性 PD 患者和 12 名匹配的健康对照者中,测量了空腹过夜后 6 个月内的血清 IGF-1 和生长激素(GH)水平。基于这些结果,在另外 6 名未经治疗的 PD 患者中测量了血清 IGF-1。

结果

在患者和对照组中,IGF-1 值在整个期间均保持稳定(r=0.83-0.93)。在所有时间点,治疗后的 PD 患者的 IGF-1 值均明显高于对照组(均 p<0.001)。患者和对照组之间的血清 GH 水平无显着差异。接收者操作特征显示,用于区分治疗患者和对照组的截止值为 114ng/ml(曲线下面积=0.90)。在患者组中,较高的血清 IGF-1 水平与较短的病程相关(r=-0.56,p=0.001)。在健康对照组中,较高的 IGF-1 与运动表现略有受损相关,这通过统一帕金森病评定量表运动评分来测量(r=0.46,p=0.005)。在未经治疗的患者组中,血清 IGF-1 水平明显高于健康对照组(p<0.001)。应用 114ng/ml 的截止值,所有未经治疗的患者均正确分类为 PD 患者。

结论

升高的 IGF-1 可能是早期 PD 及潜在亚临床多巴胺能功能障碍的有趣血清标志物。

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