Department of Geriatric Medicine, Oslo University Hospital, 0450, Oslo, Norway.
Bevital AS, 5021, Bergen, Norway.
Alzheimers Res Ther. 2024 Jul 27;16(1):167. doi: 10.1186/s13195-024-01531-7.
Sex differences in neuroinflammation could contribute to women's increased risk of Alzheimer's disease (AD), providing rationale for exploring sex-specific AD biomarkers. In AD, dysregulation of the kynurenine pathway (KP) contributes to neuroinflammation and there is some evidence of sex differences in KP metabolism. However, the sex-specific associations between KP metabolism and biomarkers of AD and neuroinflammation need to be explored further.
Here we investigate sex differences in cerebrospinal fluid concentrations of seven KP metabolites and sex-specific associations with established AD biomarkers and neopterin, an indicator of neuroinflammation. This study included 311 patients with symptomatic AD and 105 age-matched cognitively unimpaired (CU) controls, followed for up to 5 years.
We found sex differences in KP metabolites in the AD group, with higher levels of most metabolites in men, while there were no sex differences in the CU group. In line with this, more KP metabolites were significantly altered in AD men compared to CU men, and there was a trend in the same direction in AD women. Furthermore, we found sex-specific associations between kynurenic acid and the kynurenic acid/quinolinic acid ratio with neopterin, but no sex differences in the associations between KP metabolites and clinical progression.
In our cohort, sex differences in KP metabolites were restricted to AD patients. Our results suggest that dysregulation of the KP due to increased inflammation could contribute to higher AD risk in women.
神经炎症中的性别差异可能导致女性阿尔茨海默病(AD)风险增加,这为探索针对特定性别的 AD 生物标志物提供了依据。在 AD 中,犬尿氨酸途径(KP)的失调会导致神经炎症,并且 KP 代谢存在一些性别差异的证据。然而,KP 代谢与 AD 和神经炎症的生物标志物之间的特定性别关联仍需要进一步探索。
本研究旨在探讨脑脊液中 7 种 KP 代谢物的性别差异,以及与既定 AD 生物标志物和神经炎症标志物新蝶呤之间的性别特异性关联。本研究纳入了 311 名有症状的 AD 患者和 105 名年龄匹配的认知正常(CU)对照者,随访时间长达 5 年。
我们发现 AD 组中存在 KP 代谢物的性别差异,男性中大多数代谢物的水平较高,而 CU 组中则没有性别差异。与此一致的是,与 CU 男性相比,AD 男性中有更多的 KP 代谢物发生了显著变化,AD 女性也呈现出同样的趋势。此外,我们发现犬尿酸和犬尿酸/喹啉酸比值与新蝶呤之间存在性别特异性关联,但 KP 代谢物与临床进展之间的关联没有性别差异。
在我们的队列中,KP 代谢物的性别差异仅限于 AD 患者。我们的结果表明,由于炎症增加导致的 KP 失调可能导致女性 AD 风险增加。