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Factors Determining Disease Duration in Alzheimer's Disease: A Postmortem Study of 103 Cases Using the Kaplan-Meier Estimator and Cox Regression

机译:确定阿尔茨海默氏病病程的因素:使用Kaplan-Meier估计量和Cox回归进行的103例死后研究

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Factors associated with duration of dementia in a consecutive series of 103 Alzheimer's disease (AD) cases were studied using the Kaplan-Meier estimator and Cox regression analysis (proportional hazard model). Mean disease duration was 7.1 years (range: 6 weeks-30 years, standard deviation = 5.18); 25% of cases died within four years, 50% within 6.9 years, and 75% within 10 years. Familial AD cases (FAD) had a longer duration than sporadic cases (SAD), especially cases linked to presenilin (PSEN) genes. No significant differences in duration were associated with age, sex, or apolipoprotein E (Apo E) genotype. Duration was reduced in cases with arterial hypertension. Cox regression analysis suggested longer duration was associated with an earlier disease onset and increased senile plaque (SP) and neurofibrillary tangle (NFT) pathology in the orbital gyrus (OrG), CA1 sector of the hippocampus, and nucleus basalis of Meynert (NBM). The data suggest shorter disease duration in SAD and in cases with hypertensive comorbidity. In addition, degree of neuropathology did not influence survival, but spread of SP/NFT pathology into the frontal lobe, hippocampus, and basal forebrain was associated with longer disease duration.
机译:使用Kaplan-Meier估计量和Cox回归分析(比例风险模型)研究了连续103例阿尔茨海默氏病(AD)病例中与痴呆持续时间相关的因素。平均疾病持续时间为7.1年(范围:6周至30年,标准差= 5.18); 25%的病例在4年内死亡,50%的病例在6.9年内死亡,75%的病例在10年内死亡。家族性AD病例(FAD)的持续时间比散发性病例(SAD)更长,尤其是与早老素(PSEN)基因相关的病例。持续时间与年龄,性别或载脂蛋白E(Apo E)基因型无明显差异。动脉高血压患者的病程缩短。 Cox回归分析表明,更长的持续时间与更早的疾病发作以及眶回​​(OrG),海马CA1区和Meynert核基底层(NBM)的老年斑(SP)和神经原纤维缠结(NFT)病理增加有关。数据表明,SAD和高血压合并症患者的病程较短。此外,神经病理学程度不影响生存,但SP / NFT病理学扩散至额叶,海马和基底前脑与更长的疾病持续时间有关。

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