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PMID |
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TITLE |
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Caffeine Consumption, Psychological Distress, and Insomnia in a Cohort of Individuals with Depression. |
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ABSTRACT |
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INTRODUCTION |
NlmCategory: UNASSIGNED |
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 |
NlmCategory: UNASSIGNED |
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. Survey data and genetic information were sourced from the Australian Genetics of Depression Study (AGDS [ = 20,689, % = 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 |
NlmCategory: UNASSIGNED |
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. Survey data and genetic information were sourced from the Australian Genetics of Depression Study (AGDS [ = 20,689, % = 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. The highest consumers of caffeine reported higher psychological distress measured by the Kessler 10 scale (β = 1.21, SE = 0.25, = 1.4 × 10 ) compared to the lowest consumers. Consumption was associated with 2 genetic variants with effect sizes ∼0.35 additional caffeinated drinks/day between opposite homozygotes ( < 0.005). A deletion near was associated with 10% increased odds of reporting caffeine susceptibility (OR = 1.1 per deletion [95% CI: 1.04-1.17], = 0.002). |
CONCLUSIONS |
NlmCategory: UNASSIGNED |
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. Survey data and genetic information were sourced from the Australian Genetics of Depression Study (AGDS [ = 20,689, % = 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. The highest consumers of caffeine reported higher psychological distress measured by the Kessler 10 scale (β = 1.21, SE = 0.25, = 1.4 × 10 ) compared to the lowest consumers. Consumption was associated with 2 genetic variants with effect sizes ∼0.35 additional caffeinated drinks/day between opposite homozygotes ( < 0.005). A deletion near was associated with 10% increased odds of reporting caffeine susceptibility (OR = 1.1 per deletion [95% CI: 1.04-1.17], = 0.002). 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. |
© 2025 The Author(s). Published by S. Karger AG, Basel. |
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DATE PUBLISHED |
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HISTORY |
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PUBSTATUS |
PUBSTATUSDATE |
received |
2024/11/01 |
accepted |
2025/03/13 |
pmc-release |
2025/09/24 |
medline |
2025/05/02 11:07 |
pubmed |
2025/05/02 11:06 |
entrez |
2025/05/02 04:28 |
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AUTHORS |
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NAME |
COLLECTIVENAME |
LASTNAME |
FORENAME |
INITIALS |
AFFILIATION |
AFFILIATIONINFO |
McIntosh HA |
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McIntosh |
Harry A |
HA |
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Child Health Research Centre, The University of Queensland, Brisbane, QLD, Australia. |
Borgas AJ |
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Borgas |
Aleah J |
AJ |
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School of Psychology, The University of Queensland, Brisbane, QLD, Australia. |
Aouira N |
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Aouira |
Nisreen |
N |
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School of Public Health, The University of Queensland, Brisbane, QLD, Australia. |
Mitchell BL |
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Mitchell |
Brittany L |
BL |
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QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia. |
Crouse JJ |
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Crouse |
Jacob J |
JJ |
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Youth Mental Health and Technology Team, Brain and Mind Centre, The University of Sydney, Sydney, NSW, Australia. |
Medland SE |
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Medland |
Sarah E |
SE |
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QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia. |
Hickie IB |
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Hickie |
Ian B |
IB |
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Youth Mental Health and Technology Team, Brain and Mind Centre, The University of Sydney, Sydney, NSW, Australia. |
Wray NR |
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Wray |
Naomi R |
NR |
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Queensland Brain Institute, The University of Queensland, Brisbane, QLD, Australia. |
Martin NG |
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Martin |
Nicholas G |
NG |
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QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia. |
Middeldorp CM |
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Middeldorp |
Christel M |
CM |
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Child and Youth Mental Health Service, Children's Health Queensland Hospital and Health Service, Brisbane, QLD, Australia. |
Byrne EM |
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Byrne |
Enda M |
EM |
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Child Health Research Centre, The University of Queensland, Brisbane, QLD, Australia. |
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INVESTIGATORS |
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JOURNAL |
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VOLUME: 11 |
ISSUE: 1 |
TITLE: Complex psychiatry |
ISOABBREVIATION: Complex Psychiatry |
YEAR: 2025 |
MONTH: |
DAY: |
MEDLINEDATE: |
SEASON: Jan-Dec |
CITEDMEDIUM: Print |
ISSN: 2673-3005 |
ISSNTYPE: Print |
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MEDLINE JOURNAL |
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MEDLINETA: Complex Psychiatry |
COUNTRY: Switzerland |
ISSNLINKING: 2673-298X |
NLMUNIQUEID: 101764441 |
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PUBLICATION TYPE |
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PUBLICATIONTYPE TEXT |
Journal Article |
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COMMENTS AND CORRECTIONS |
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GRANTS |
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GENERAL NOTE |
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KEYWORDS |
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KEYWORD |
ADORA2A |
AHR |
CYP1A1 |
CYP1A2 |
Caffeine |
Insomnia |
Psychiatric disorders |
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MESH HEADINGS |
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SUPPLEMENTARY MESH |
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GENE SYMBOLS |
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CHEMICALS |
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OTHER ID's |
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