Division of Systems Medical Science, Center for Medical Science, Fujita Health University, Toyoake, Japan.
Int J Neuropsychopharmacol. 2024 Oct 1;27(10). doi: 10.1093/ijnp/pyae047.
Altered brain energy metabolism is implicated in Alzheimer disease (AD). Limited and conflicting studies on brain pH changes, indicative of metabolic alterations associated with neural activity, warrant a comprehensive investigation into their relevance in this neurodegenerative condition. Furthermore, the relationship between these pH changes and established AD neuropathological evaluations, such as Braak staging, remains unexplored.
We conducted quantitative meta-analyses on postmortem brain and cerebrospinal fluid pH in patients with AD and non-AD controls using publicly available demographic data. We collected raw pH data from studies in the NCBI GEO, PubMed, and Google Scholar databases.
Our analysis of 20 datasets (723 patient samples and 524 control samples) using a random-effects model showed a significant decrease in brain and cerebrospinal fluid pH in patients compared with controls (Hedges' g = -0.57, P < .0001). This decrease remained significant after considering postmortem interval, age at death, and sex. Notably, pH levels were negatively correlated with Braak stage, indicated by the random-effects model of correlation coefficients from 15 datasets (292 patient samples and 159 control samples) (adjusted r = -0.26, P < .0001). Furthermore, brain pH enhanced the discriminative power of the APOEε4 allele, the most prevalent risk gene for AD, in distinguishing patients from controls in a meta-analysis of 4 combined datasets (95 patient samples and 87 control samples).
The significant decrease in brain pH in AD underlines its potential role in disease progression and diagnosis. This decrease, potentially reflecting neural hyperexcitation, could enhance our understanding of neurodegenerative pathology and aid in developing diagnostic strategies.
改变的大脑能量代谢与阿尔茨海默病(AD)有关。有限且相互矛盾的研究表明,大脑 pH 值的变化表明与神经活动相关的代谢改变,这需要对其在这种神经退行性疾病中的相关性进行全面研究。此外,这些 pH 值变化与已经建立的 AD 神经病理学评估(如 Braak 分期)之间的关系仍未得到探索。
我们使用公开的人口统计学数据对 AD 患者和非 AD 对照者的死后大脑和脑脊液 pH 值进行了定量荟萃分析。我们从 NCBI GEO、PubMed 和 Google Scholar 数据库中的研究中收集了原始 pH 值数据。
我们使用随机效应模型对 20 个数据集(723 例患者样本和 524 例对照样本)进行了分析,结果显示患者的大脑和脑脊液 pH 值与对照者相比显著降低(Hedges' g=-0.57,P<.0001)。在考虑了死后间隔时间、死亡时的年龄和性别后,这种降低仍然显著。值得注意的是,pH 值与 Braak 分期呈负相关,这是通过来自 15 个数据集(292 例患者样本和 159 例对照样本)的相关系数的随机效应模型得出的(调整 r=-0.26,P<.0001)。此外,在对 4 个合并数据集(95 例患者样本和 87 例对照样本)的荟萃分析中,大脑 pH 值增强了 APOEε4 等位基因(AD 最常见的风险基因)区分患者和对照者的判别能力。
AD 中大脑 pH 值的显著降低突出了其在疾病进展和诊断中的潜在作用。这种降低可能反映了神经兴奋过度,有助于我们更好地理解神经退行性病理,并有助于开发诊断策略。