Christchurch Health and Development Study, Department of Psychological Medicine, University of Otago Christchurch, Christchurch Central City, Christchurch 8011, New Zealand.
Department of Psychological Medicine, University of Otago, Wellington, New Zealand.
Psychol Med. 2023 Feb;53(3):987-994. doi: 10.1017/S0033291721002415. Epub 2021 Jun 17.
This study examined the association between methamphetamine use and psychotic symptoms in a New Zealand general population birth cohort ( = 1265 at birth).
At age 18, 21, 25, 30, and 35, participants reported on their methamphetamine use and psychotic symptoms in the period since the previous interview. Generalized estimating equations modelled the association between methamphetamine use and psychotic symptoms (percentage reporting any symptom, and number of symptoms per participant). Confounding factors included childhood individual characteristics, family socioeconomic circumstances and family functioning. Long term effects of methamphetamine use on psychotic symptoms were assessed by comparing the incidence of psychotic symptoms at age 30-35 for those with and without a history of methamphetamine use prior to age 30.
After adjusting for confounding factors and time-varying covariate factors including concurrent cannabis use, methamphetamine use was associated with a modest increase in psychosis risk over five waves of data (adjusted odds ratio (OR) 1.33, 95% confidence interval (CI) 1.03-1.72 for the percentage measure; and IRR 1.24, 95% CI 1.02-1.50 for the symptom count measure). The increased risk of psychotic symptoms was concentrated among participants who had used at least weekly at any point (adjusted OR 2.85, 95% CI 1.21-6.69). Use of methamphetamine less than weekly was not associated with increased psychosis risk. We found no evidence for a persistent vulnerability to psychosis in the absence of continuing methamphetamine use.
Methamphetamine use is associated with increased risk of psychotic symptoms in the general population. Increased risk is chiefly confined to people who ever used regularly (at least weekly), and recently.
本研究在新西兰一般人群出生队列中(出生时为 1265 人),考察了甲基苯丙胺使用与精神病症状之间的关联。
在 18、21、25、30 和 35 岁时,参与者报告了他们在之前访谈后的时期内使用甲基苯丙胺和出现精神病症状的情况。使用广义估计方程对甲基苯丙胺使用与精神病症状之间的关系进行建模(报告任何症状的百分比,以及每位参与者的症状数)。混杂因素包括儿童个体特征、家庭社会经济状况和家庭功能。通过比较 30-35 岁时有和无 30 岁前甲基苯丙胺使用史的参与者的精神病症状发生率,评估了甲基苯丙胺使用对精神病症状的长期影响。
在校正混杂因素和时间变化的协变量因素(包括同期大麻使用)后,甲基苯丙胺使用与五次数据波中精神病风险的适度增加相关(百分比测量的调整后比值比(OR)为 1.33,95%置信区间(CI)为 1.03-1.72;症状数测量的发病率比(IRR)为 1.24,95%CI 为 1.02-1.50)。风险增加的精神病症状主要集中在曾有过至少每周一次使用的参与者中(调整后的 OR 为 2.85,95%CI 为 1.21-6.69)。每周使用少于一次的甲基苯丙胺与增加精神病风险无关。我们没有发现在没有持续使用甲基苯丙胺的情况下,精神病易感性持续存在的证据。
在一般人群中,甲基苯丙胺使用与精神病症状风险增加相关。风险增加主要局限于曾有过定期(至少每周)和最近使用的人群。