Harry A McIntosh, Aleah J Borgas, Nisreen Aouira, Brittany L Mitchell, Jacob J Crouse, Sarah E Medland, Ian B Hickie, Naomi R Wray, Nicholas G Martin, Christel M Middeldorp, Enda M Byrne
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Associations between caffeine consumption and symptoms of distress and sleep disturbance, as well as 9 genetic variants associated with caffeine consumption behaviour, were assessed using linear regression.</p><p><strong>Results: </strong>The highest consumers of caffeine reported higher psychological distress measured by the Kessler 10 scale (β = 1.21, SE = 0.25, <i>p</i> = 1.4 × 10<sup>-6</sup>) compared to the lowest consumers. Consumption was associated with 2 genetic variants with effect sizes ∼0.35 additional caffeinated drinks/day between opposite homozygotes (<i>p</i> < 0.005). A deletion near <i>MMS22L/POU3F2</i> was associated with 10% increased odds of reporting caffeine susceptibility (OR = 1.1 per deletion [95% CI: 1.04-1.17], <i>p</i> = 0.002).</p><p><strong>Conclusions: </strong>Higher rates of caffeine consumption were associated with higher levels of psychological distress, but not insomnia, in individuals with a history of depression. While the direction of causality is unclear, caffeine consumption may be a modifiable factor to reduce distress in individuals susceptible to mental health problems. Some of the previous findings of common variant associations with caffeine consumption and susceptibility were replicated.</p>","PeriodicalId":72654,"journal":{"name":"Complex psychiatry","volume":"11 1","pages":"37-49"},"PeriodicalIF":0.0000,"publicationDate":"2025-03-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12043281/pdf/","citationCount":"0","resultStr":"{\"title\":\"Caffeine Consumption, Psychological Distress, and Insomnia in a Cohort of Individuals with Depression.\",\"authors\":\"Harry A McIntosh, Aleah J Borgas, Nisreen Aouira, Brittany L Mitchell, Jacob J Crouse, Sarah E Medland, Ian B Hickie, Naomi R Wray, Nicholas G Martin, Christel M Middeldorp, Enda M Byrne\",\"doi\":\"10.1159/000545393\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Introduction: </strong>Caffeine is a widely consumed psychoactive compound that can cause anxiety and sleep difficulties, in part due to genetic variation. We investigated the association between caffeine consumption, psychological distress, and sleep difficulties in a genetically informative cohort of individuals with a history of depression.</p><p><strong>Methods: </strong>Survey data and genetic information were sourced from the Australian Genetics of Depression Study (AGDS [<i>n</i> = 20,689, %<sub>female</sub> = 75%, mean age = 43 ± 15 years]). Associations between caffeine consumption and symptoms of distress and sleep disturbance, as well as 9 genetic variants associated with caffeine consumption behaviour, were assessed using linear regression.</p><p><strong>Results: </strong>The highest consumers of caffeine reported higher psychological distress measured by the Kessler 10 scale (β = 1.21, SE = 0.25, <i>p</i> = 1.4 × 10<sup>-6</sup>) compared to the lowest consumers. Consumption was associated with 2 genetic variants with effect sizes ∼0.35 additional caffeinated drinks/day between opposite homozygotes (<i>p</i> < 0.005). A deletion near <i>MMS22L/POU3F2</i> was associated with 10% increased odds of reporting caffeine susceptibility (OR = 1.1 per deletion [95% CI: 1.04-1.17], <i>p</i> = 0.002).</p><p><strong>Conclusions: </strong>Higher rates of caffeine consumption were associated with higher levels of psychological distress, but not insomnia, in individuals with a history of depression. While the direction of causality is unclear, caffeine consumption may be a modifiable factor to reduce distress in individuals susceptible to mental health problems. 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引用次数: 0
摘要
简介:咖啡因是一种广泛使用的精神活性化合物,可引起焦虑和睡眠困难,部分原因是遗传变异。我们调查了咖啡因摄入、心理困扰和睡眠困难之间的关系,研究对象是一组有抑郁症病史的遗传信息丰富的个体。方法:调查数据和遗传信息来源于澳大利亚抑郁症遗传学研究(AGDS [n = 20,689, %女性= 75%,平均年龄= 43±15岁])。使用线性回归评估了咖啡因摄入与焦虑和睡眠障碍症状之间的关系,以及与咖啡因摄入行为相关的9种基因变异。结果:通过Kessler 10量表(β = 1.21, SE = 0.25, p = 1.4 × 10-6)测量,咖啡因摄入量最高的人比咖啡因摄入量最低的人报告了更高的心理困扰。相反纯合子之间的咖啡因摄入量与2种遗传变异相关,效应值为0.35杯/天(p < 0.005)。MMS22L/POU3F2附近的缺失与报告咖啡因易感性的几率增加10%相关(每个缺失OR = 1.1 [95% CI: 1.04-1.17], p = 0.002)。结论:对于有抑郁史的人来说,咖啡因摄入的比例越高,心理困扰程度越高,但与失眠无关。虽然因果关系的方向尚不清楚,但咖啡因的摄入可能是一个可改变的因素,可以减少易受精神健康问题影响的个体的痛苦。之前发现的一些与咖啡因摄入和易感性相关的常见变异被重复了。
Caffeine Consumption, Psychological Distress, and Insomnia in a Cohort of Individuals with Depression.
Introduction: Caffeine is a widely consumed psychoactive compound that can cause anxiety and sleep difficulties, in part due to genetic variation. We investigated the association between caffeine consumption, psychological distress, and sleep difficulties in a genetically informative cohort of individuals with a history of depression.
Methods: Survey data and genetic information were sourced from the Australian Genetics of Depression Study (AGDS [n = 20,689, %female = 75%, mean age = 43 ± 15 years]). Associations between caffeine consumption and symptoms of distress and sleep disturbance, as well as 9 genetic variants associated with caffeine consumption behaviour, were assessed using linear regression.
Results: The highest consumers of caffeine reported higher psychological distress measured by the Kessler 10 scale (β = 1.21, SE = 0.25, p = 1.4 × 10-6) compared to the lowest consumers. Consumption was associated with 2 genetic variants with effect sizes ∼0.35 additional caffeinated drinks/day between opposite homozygotes (p < 0.005). A deletion near MMS22L/POU3F2 was associated with 10% increased odds of reporting caffeine susceptibility (OR = 1.1 per deletion [95% CI: 1.04-1.17], p = 0.002).
Conclusions: Higher rates of caffeine consumption were associated with higher levels of psychological distress, but not insomnia, in individuals with a history of depression. While the direction of causality is unclear, caffeine consumption may be a modifiable factor to reduce distress in individuals susceptible to mental health problems. Some of the previous findings of common variant associations with caffeine consumption and susceptibility were replicated.