Institute of Physiology, Department of Biology, Faculty of Pharmacy, University of Belgrade, Belgrade, Serbia.
J Gerontol A Biol Sci Med Sci. 2010 Dec;65(12):1269-74. doi: 10.1093/gerona/glq148. Epub 2010 Aug 30.
Chromosomal alterations are a feature of both aging and Alzheimer's disease (AD). This study examined if premature centromere division (PCD), a chromosomal instability indicator increased in AD, is correlated with aging or, instead, represents a de novo chromosomal alteration due to accelerating aging in AD. PCD in peripheral blood lymphocytes was determined in sporadic AD patients and gender and age-matched unaffected controls. Metaphase nuclei were analyzed for chromosomes showing PCD, X chromosomes with PCD (PCD,X), and acrocentric chromosomes showing PCD. AD patients, regardless of age, demonstrated increased PCD on any chromosome and PCD on acrocentric chromosomes in both genders, whereas an increase in frequency of PCD,X was expressed only in women. This cytogenetic analysis suggests that PCD is a feature of AD, rather than an epiphenomenon of chronological aging, and may be useful as a physiological biomarker that can be used for disease diagnosis.
染色体改变是衰老和阿尔茨海默病(AD)的共同特征。本研究探讨了 AD 中增加的过早着丝粒分裂(PCD),一种染色体不稳定性指标,是否与衰老相关,或者它是否代表由于 AD 中衰老加速而导致的新的染色体改变。在散发性 AD 患者和性别及年龄匹配的未受影响的对照组中,测定外周血淋巴细胞中的 PCD。分析显示 PCD 的中期核、具有 PCD 的 X 染色体(PCD,X)和具有 PCD 的近端着丝粒染色体。无论年龄大小,AD 患者的任何染色体上均显示出 PCD 增加,两性的近端着丝粒染色体上也显示出 PCD 增加,而 PCD,X 的频率增加仅在女性中表达。这种细胞遗传学分析表明,PCD 是 AD 的一个特征,而不是与年龄相关的衰老的表象,并且可以作为生理生物标志物用于疾病诊断。