Department of Psychiatry, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Psychiatry Residency Training Program, George Washington University, Washington, District of Columbia, USA.
J Gerontol A Biol Sci Med Sci. 2024 Mar 1;79(3). doi: 10.1093/gerona/glad228.
Persistent inflammation related to aging ("inflammaging") is exacerbated by chronic infections and contributes to frailty in older adults. We hypothesized associations between Toxoplasma gondii (T. gondii), a common parasite causing an oligosymptomatic unremitting infection, and frailty, and secondarily between T. gondii and previously reported markers of immune activation in frailty.
We analyzed available demographic, social, and clinical data in Spanish and Portuguese older adults [N = 601; age: mean (SD) 77.3 (8.0); 61% women]. Plasma T. gondii immunoglobulin G (IgG) serointensity was measured with an enzyme-linked immunosorbent assay. The Fried criteria were used to define frailty status. Validated translations of Mini-Mental State Examination, Geriatric Depression Scale, and the Charlson Comorbidity Index were used to evaluate confounders. Previously analyzed biomarkers that were significantly associated with frailty in both prior reports and the current study, and also related to T. gondii serointensity, were further accounted for in multivariable logistic models with frailty as outcome.
In T. gondii-seropositives, there was a significant positive association between T. gondii IgG serointensity and frailty, accounting for age (p = .0002), and resisting adjustment for multiple successive confounders. Among biomarkers linked with frailty, kynurenine/tryptophan and soluble tumor necrosis factor receptor II were positively associated with T. gondii serointensity in seropositives (p < .05). Associations with other biomarkers were not significant.
This first reported association between T. gondii and frailty is limited by a cross-sectional design and warrants replication. While certain biomarkers of inflammaging were associated with both T. gondii IgG serointensity and frailty, they did not fully mediate the T. gondii-frailty association.
与衰老相关的持续性炎症(“炎症老化”)会因慢性感染而加剧,并导致老年人虚弱。我们假设,一种常见的寄生虫——刚地弓形虫(Toxoplasma gondii),它引起一种症状轻微但持续存在的感染,与虚弱之间存在关联,其次是刚地弓形虫与之前报道的虚弱时免疫激活标志物之间存在关联。
我们分析了西班牙和葡萄牙老年人(N=601;年龄:平均(SD)77.3(8.0);61%为女性)现有的人口统计学、社会和临床数据。使用酶联免疫吸附试验测量血浆刚地弓形虫免疫球蛋白 G(IgG)的血清强度。使用 Fried 标准定义虚弱状态。使用经验证的简易精神状态检查量表、老年抑郁量表和 Charlson 合并症指数的翻译版本来评估混杂因素。在多变量逻辑模型中,将与虚弱相关且与刚地弓形虫血清强度相关的先前分析的生物标志物作为结局,进一步考虑与虚弱的关联。
在刚地弓形虫血清阳性者中,刚地弓形虫 IgG 血清强度与虚弱之间存在显著正相关,且与年龄相关(p=0.0002),并能抵抗多个连续混杂因素的调整。在与虚弱相关的生物标志物中,犬尿氨酸/色氨酸和可溶性肿瘤坏死因子受体 II 与刚地弓形虫血清阳性者的刚地弓形虫血清强度呈正相关(p<0.05)。与其他生物标志物的关联不显著。
这是首次报道的刚地弓形虫与虚弱之间的关联受到横断面设计的限制,需要进一步验证。虽然某些炎症老化的生物标志物与刚地弓形虫 IgG 血清强度和虚弱都相关,但它们并不能完全介导刚地弓形虫与虚弱之间的关联。