Pluta Ryszard
Department of Pathophysiology, Medical University of Lublin, 20-090 Lublin, Poland.
Life (Basel). 2025 Jul 21;15(7):1146. doi: 10.3390/life15071146.
This comment focuses on the contribution of experimental brain ischemia to the overwhelming incidence of Alzheimer's disease in women as presented by Lohkamp et al. in 2025, 15, 333. The authors showed that in Alzheimer's disease and ischemic stroke there are sex-dependent adaptations in the form of cross-links and vice versa. It was emphasized that the high longevity of women in itself does not explain the mechanisms underlying the biological differences between the sexes causing a female predominance in the development of Alzheimer's disease. Differences were demonstrated between males and females: female APP/PS1 mice had greater amyloid deposition, hyperactivity, lower body weight, and reduced cerebral blood flow, as well as less neuroinflammation, which the authors suggest may have potential neuroprotection. It should be noted that some of the information presented in the article by Lohkamp et al. raises more questions than answers. Therefore, future studies should consider, for example, studies using single-cell technologies that can provide insight into the timing and sequence of cellular dysfunctions across sexes and analyze the continuity of changes over time, starting from short-term observations of a few days and ending with long-term observations of a year or more, to assess the continuity and differentiation of changes.
本评论聚焦于Lohkamp等人于2025年发表在第15卷第333页的文章中所阐述的实验性脑缺血对女性阿尔茨海默病高发率的影响。作者表明,在阿尔茨海默病和缺血性卒中中,存在以交联形式呈现的性别依赖性适应性变化,反之亦然。需要强调的是,女性的高寿命本身并不能解释导致女性在阿尔茨海默病发展中占主导地位的性别生物学差异背后的机制。研究显示了雄性和雌性之间的差异:雌性APP/PS1小鼠有更多的淀粉样蛋白沉积、多动、体重减轻、脑血流量减少,以及神经炎症较少,作者认为这可能具有潜在的神经保护作用。应当指出的是,Lohkamp等人文章中呈现的一些信息引发的问题比答案更多。因此,未来的研究应该考虑,例如,使用单细胞技术的研究,这些研究能够洞察不同性别细胞功能障碍的时间和顺序,并分析从几天的短期观察到一年或更长时间的长期观察期间变化的连续性,以评估变化的连续性和差异性。