Hoy Nicholas, Waszczuk Monika, Sunderland Matthew, Lynch Samantha J, Sachdev Perminder S, Brodaty Henry, Reppermund Simone, Mewton Louise
The Matilda Centre for Research in Mental Health and Substance Use, University of Sydney, Sydney, Australia.
Department of Psychology, Rosalind Franklin University of Medicine and Science, North Chicago, IL, USA.
Psychol Med. 2025 Feb 4;55:e5. doi: 10.1017/S0033291724003490.
The structure of psychopathology can be organized hierarchically into a set of transdiagnostic dimensional phenotypes. No studies have examined whether these phenotypes are associated with brain structure or dementia in older adults.
Data were drawn from a longitudinal study of older adults aged 70-90 years at baseline ( = 1072; 44.8% male). Confirmatory factor models were fit to baseline psychiatric symptoms, with model fit assessed via traditional fit indices, model-based reliability estimates, and evaluation of model parameters. Bayesian plausible values were generated from the best-fitting model for use in subsequent analyses. Linear mixed models examined intraindividual change in global and regional gray matter volume (GMV) and cortical thickness over 6 years. Logistic regression examined whether symptom dimensions predicted incident dementia over 12 years.
A higher-order model showed a good fit to the data (BIC = 28,691.85; ssaBIC = 28,396.47; CFI = 0.926; TLI = 0.92; RMSEA = 0.047), including a general factor and lower-order dimensions of internalizing, disinhibited externalizing, and substance use. Baseline symptom dimensions did not predict change over time in total cortical and subcortical GMV or average cortical thickness; regional GMV or cortical thickness in the frontal, parietal, temporal, or occipital lobes; or regional GMV in the hippocampus and cerebellum (all -values >0.5). Finally, baseline symptom dimensions did not predict incident dementia across follow-ups (all -values >0.5).
We found no evidence that transdiagnostic dimensions are associated with gray matter structure or dementia in older adults. Future research should examine these relationships using psychiatric indicators capturing past history of chronic mental illness rather than current symptoms.
精神病理学结构可分层组织为一组跨诊断维度表型。尚无研究探讨这些表型是否与老年人的脑结构或痴呆症相关。
数据来自一项对基线年龄为70 - 90岁的老年人的纵向研究(n = 1072;44.8%为男性)。验证性因素模型用于拟合基线精神症状,通过传统拟合指数、基于模型的可靠性估计以及模型参数评估来评估模型拟合情况。从最佳拟合模型生成贝叶斯合理值用于后续分析。线性混合模型研究了6年期间全脑和区域灰质体积(GMV)以及皮质厚度的个体内变化。逻辑回归分析了症状维度是否能预测12年内的新发痴呆症。
一个高阶模型显示与数据拟合良好(BIC = 28,691.85;ssaBIC = 28,396.47;CFI = 0.926;TLI = 0.92;RMSEA = 0.047),包括一个一般因素以及内化、去抑制外化和物质使用的低阶维度。基线症状维度并未预测总皮质和皮质下GMV或平均皮质厚度随时间的变化;额叶、顶叶、颞叶或枕叶的区域GMV或皮质厚度;或海马体和小脑的区域GMV(所有p值>0.5)。最后,基线症状维度在随访期间并未预测新发痴呆症(所有p值>0.5)。
我们没有发现证据表明跨诊断维度与老年人的灰质结构或痴呆症相关。未来的研究应该使用捕捉慢性精神疾病既往史而非当前症状的精神指标来检验这些关系。