Center for Neuropsychiatric Schizophrenia Research (CNSR) and Center for Clinical Intervention and Neuropsychiatric Schizophrenia Research (CINS), Mental Health Center Glostrup, Glostrup, Denmark.
Department of Psychology, University of Copenhagen, Copenhagen, Denmark.
Psychol Med. 2021 Jul;51(9):1570-1580. doi: 10.1017/S0033291720000409. Epub 2020 Mar 11.
The typical onset of schizophrenia coincides with the maturational peak in cognition; however, for a significant proportion of patients the onset is before age 18 and after age 30 years. While cognitive deficits are considered core features of schizophrenia, few studies have directly examined the impact of age of illness onset on cognition.
The aim of the study was to examine if the effects of age on cognition differ between healthy controls (HCs) and patients with schizophrenia at illness onset. We examined 156 first-episode antipsychotic-naïve patients across a wide age span (12-43 years), and 161 age- and sex-matched HCs. Diagnoses were made according to ICD-10 criteria. Cognition was assessed using the Brief Assessment of Cognition in Schizophrenia (BACS), and IQ was estimated using subtests from the Wechsler adult- or child-intelligence scales. Multivariate analysis of covariance (MANCOVA) was used to examine linear and quadratic effects of age on cognitive scores and interactions by group, including sex and parental socioeconomic status as covariates.
There was a significant overall effect of age on BACS and IQ (p < 0.001). Significant group-by-age interactions for verbal memory (for age-squared, p = 0.009), and digit sequencing (for age, p = 0.01; age-squared, p < 0.001), indicated differential age-related trajectories between patients and HCs.
Cognitive functions showing protracted maturation into adulthood, such as verbal memory and verbal working memory, may be particularly impaired in both early- and late-schizophrenia onset. Our findings indicate a potential interaction between the timing of neurodevelopmental maturation and a possible premature age effect in late-onset schizophrenia.
精神分裂症的典型发病期与认知成熟高峰期相吻合;然而,对于相当一部分患者,发病期在 18 岁之前和 30 岁之后。虽然认知缺陷被认为是精神分裂症的核心特征,但很少有研究直接研究发病年龄对认知的影响。
本研究旨在探讨健康对照组(HCs)和首发抗精神病药物治疗的精神分裂症患者之间,年龄对认知的影响是否不同。我们研究了 156 名首发、未经抗精神病药物治疗、年龄跨度较大(12-43 岁)的患者,以及 161 名年龄和性别匹配的 HCs。诊断依据 ICD-10 标准。使用简明精神分裂症认知评估量表(BACS)评估认知,使用韦氏成人或儿童智力量表的子测验估计智商。采用协方差分析(MANCOVA)来检验认知评分的线性和二次年龄效应以及组间的交互作用,包括性别和父母社会经济地位作为协变量。
BACS 和智商的总体年龄效应显著(p < 0.001)。言语记忆(年龄平方,p = 0.009)和数字排序(年龄,p = 0.01;年龄平方,p < 0.001)存在显著的组-年龄交互作用,表明患者和 HCs 之间存在不同的与年龄相关的轨迹。
言语记忆和言语工作记忆等成熟过程持续到成年的认知功能,可能在早发性和晚发性精神分裂症中都受到特别损害。我们的研究结果表明,神经发育成熟的时间和晚发性精神分裂症中可能的过早年龄效应之间存在潜在的相互作用。