Department of Internal Medicine and Clinical Nutrition, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Mölndal, Sweden.
J Alzheimers Dis. 2020;75(1):289-298. doi: 10.3233/JAD-190921.
Insulin-like growth factor-I (IGF-I) is important for amyloid-β (Aβ) metabolism, and also interacts with the brain vasculature. In previous IGF-I studies, it has not been evaluated whether Alzheimer's disease (AD) patients had vascular comorbidities.
A cross-sectional study of 40 consecutive non-diabetic AD patients and 36 healthy controls. We measured IGF-I in serum and cerebrospinal fluid (CSF) and also serum insulin. Mixed forms of AD and vascular dementia were excluded.
After adjustment for covariates including age, serum IGF-I level was higher in the AD group than in the controls, whereas CSF IGF-I and serum insulin were unchanged. Binary logistic regression confirmed that high serum IGF-I was associated with increased prevalence of AD [adjusted Odds Ratio (OR) = 1.83, 95% confidence interval (CI): 1.005-3.32 per standard deviation (SD) increase in serum IGF-I]. This association was more robust after exclusion of patients receiving treatment with acetylcholinesterase inhibitors or N-methyl D-aspartate (NMDA) receptor antagonists (OR = 2.23, 95 % CI: 1.10-4.48). In the total study population (n = 76) as well in the AD group (n = 40), serum IGF-I correlated negatively with CSF Aβ1-42, and CSF IGF-I correlated positively with CSF/serum albumin ratio, CSF total tau, and CSF phosphorylated tau.
In AD patients without major brain vascular comorbidities, serum but not CSF levels of IGF-I were increased after correction for covariates. This association was strengthened by exclusion of patients receiving medical treatment. Overall, the results support the notion of IGF-I resistance in mild AD dementia.
胰岛素样生长因子-I(IGF-I)对淀粉样蛋白-β(Aβ)代谢很重要,并且与大脑血管相互作用。在之前的 IGF-I 研究中,尚未评估阿尔茨海默病(AD)患者是否存在血管合并症。
这是一项连续的 40 例非糖尿病 AD 患者和 36 例健康对照者的横断面研究。我们测量了血清和脑脊液(CSF)中的 IGF-I,以及血清胰岛素。排除混合形式的 AD 和血管性痴呆。
在调整了包括年龄在内的混杂因素后,AD 组的血清 IGF-I 水平高于对照组,而 CSF IGF-I 和血清胰岛素未发生变化。二元逻辑回归证实,高血清 IGF-I 与 AD 的患病率增加相关[校正后优势比(OR)=1.83,95%置信区间(CI):血清 IGF-I 每增加 1 个标准差(SD),则增加 1.005-3.32]。排除接受乙酰胆碱酯酶抑制剂或 N-甲基-D-天冬氨酸(NMDA)受体拮抗剂治疗的患者后,该相关性更为可靠(OR=2.23,95%CI:1.10-4.48)。在总研究人群(n=76)以及 AD 组(n=40)中,血清 IGF-I 与 CSF Aβ1-42 呈负相关,CSF IGF-I 与 CSF/血清白蛋白比值、CSF 总 tau 和 CSF 磷酸化 tau 呈正相关。
在没有主要大脑血管合并症的 AD 患者中,校正混杂因素后,血清 IGF-I 水平升高,而 CSF 水平无变化。排除接受药物治疗的患者后,该相关性增强。总体而言,这些结果支持轻度 AD 痴呆中 IGF-I 抵抗的观点。