Chakrabarti Sasanka, Khemka Vineet Kumar, Banerjee Anindita, Chatterjee Gargi, Ganguly Anirban, Biswas Atanu
Department of Biochemistry, Institute of Post Graduate Medical Education and Research, Kolkata, India.
Department of Biochemistry, Institute of Post Graduate Medical Education and Research, Kolkata, India. ; Department of Biochemistry, ICARE Institute of Medical Sciences and Research, Haldia, India.
Aging Dis. 2015 Aug 1;6(4):282-99. doi: 10.14336/AD.2014.002. eCollection 2015 Aug.
Alzheimer's disease (AD), the major cause of dementia among the elderly world-wide, manifests in familial and sporadic forms, and the latter variety accounts for the majority of the patients affected by this disease. The etiopathogenesis of sporadic AD is complex and uncertain. The autopsy studies of AD brain have provided limited understanding of the antemortem pathogenesis of the disease. Experimental AD research with transgenic animal or various cell based models has so far failed to explain the complex and varied spectrum of AD dementia. The review, therefore, emphasizes the importance of AD related risk factors, especially those with metabolic implications, identified from various epidemiological studies, in providing clues to the pathogenesis of this complex disorder. Several metabolic risk factors of AD like hypercholesterolemia, hyperhomocysteinemia and type 2 diabetes have been studied extensively both in epidemiology and experimental research, while much less is known about the role of adipokines, pro-inflammatory cytokines and vitamin D in this context. Moreover, the results from many of these studies have shown a degree of variability which has hindered our understanding of the role of AD related risk factors in the disease progression. The review also encompasses the recent recommendations regarding clinical and neuropathological diagnosis of AD and brings out the inherent uncertainty and ambiguity in this area which may have a distinct impact on the outcome of various population-based studies on AD-related risk factors.
阿尔茨海默病(AD)是全球老年人痴呆的主要病因,有家族性和散发性两种形式,其中后者占受该病影响患者的大多数。散发性AD的病因发病机制复杂且尚不明确。对AD患者大脑进行尸检研究,对该疾病生前发病机制的了解有限。迄今为止,利用转基因动物或各种细胞模型进行的AD实验研究未能解释AD痴呆复杂多样的症状。因此,本综述强调了从各种流行病学研究中确定的AD相关危险因素的重要性,尤其是那些具有代谢影响的因素,它们为这种复杂疾病的发病机制提供了线索。AD的几种代谢危险因素,如高胆固醇血症、高同型半胱氨酸血症和2型糖尿病,在流行病学和实验研究中都得到了广泛研究,而在此背景下,关于脂肪因子、促炎细胞因子和维生素D的作用却知之甚少。此外,许多这些研究的结果都显示出一定程度的变异性,这阻碍了我们对AD相关危险因素在疾病进展中作用的理解。本综述还涵盖了近期关于AD临床和神经病理学诊断的建议,并揭示了该领域固有的不确定性和模糊性,这可能对各种基于人群的AD相关危险因素研究结果产生明显影响。