共 11 条
Psychiatric comorbidities in epilepsy: population co-occurrence, genetic correlations and causal effects
被引:1
|作者:
Ahlqvist, Viktor H.
[1
,2
]
Dardani, Christina
[2
,3
]
Madley-Dowd, Paul
[2
,3
]
Forbes, Harriet
[3
,4
]
Rast, Jessica
[5
,6
]
Zhong, Caichen
[5
,6
]
Gardner, Renee M.
[1
]
Dalman, Christina
[1
]
Lyall, Kristen
[5
]
Newschaffer, Craig
[7
]
Tomson, Torbjorn
[8
]
Lundberg, Michael
[1
]
Berglind, Daniel
[1
,9
]
Davies, Neil M.
[10
,11
,12
]
Lee, Brian K.
[1
,5
,6
]
Magnusson, Cecilia
[1
,9
]
Rai, Dheeraj
[2
,3
,13
,14
]
机构:
[1] Karolinska Inst, Dept Global Publ Hlth, Stockholm, Sweden
[2] Univ Bristol, Bristol Med Sch, Med Res Council, Integrat Epidemiol Unit, Bristol, England
[3] Univ Bristol, Ctr Acad Mental Hlth, Bristol Med Sch, Populat Hlth Sci, Bristol, England
[4] London Sch Hyg & Trop Med, Fac Epidemiol & Populat Hlth, London, England
[5] Drexel Univ, AJ Drexel Autism Inst, Philadelphia, PA USA
[6] Drexel Univ, Sch Publ Hlth, Dept Epidemiol & Biostat, Philadelphia, PA USA
[7] Penn State Univ, Coll Hlth & Human Dev, State Coll, PA USA
[8] Karolinska Inst, Dept Clin Neurosci, Stockholm, Sweden
[9] Ctr Epidemiol & Community Med, Reg Stockholm, Stockholm, Sweden
[10] Norwegian Univ Sci & Technol, KG Jebsen Ctr Genet Epidemiol, Dept Publ Hlth & Nursing, Trondheim, Norway
[11] UCL, Div Psychiat, London, England
[12] UCL, Dept Stat Sci, London, England
[13] Univ Bristol, NIHR Biomed Res Ctr, Bristol, England
[14] NHS Mental Hlth Trust, Avon & Wiltshire Partnership, Bristol, England
基金:
英国医学研究理事会;
美国国家卫生研究院;
瑞典研究理事会;
关键词:
neuropsychiatry;
psychiatry;
LD SCORE REGRESSION;
MENDELIAN RANDOMIZATION;
PREMATURE MORTALITY;
DETERMINANTS;
DISORDERS;
D O I:
10.1136/gpsych-2023-101201
中图分类号:
R749 [精神病学];
学科分类号:
100205 ;
摘要:
Background Psychiatric comorbidities are common in patients with epilepsy. Reasons for the co-occurrence of psychiatric conditions and epilepsy remain poorly understood. Aim We aimed to triangulate the relationship between epilepsy and psychiatric conditions to determine the extent and possible origins of these conditions. Methods Using nationwide Swedish health registries, we quantified the lifetime prevalence of psychiatric disorders in patients with epilepsy. We then used summary data from genome-wide association studies to investigate whether the identified observational associations could be attributed to a shared underlying genetic aetiology using cross-trait linkage disequilibrium score regression. Finally, we assessed the potential bidirectional relationships using two-sample Mendelian randomisation. Results In a cohort of 7 628 495 individuals, we found that almost half of the 94 435 individuals diagnosed with epilepsy were also diagnosed with a psychiatric condition in their lifetime (adjusted lifetime prevalence, 44.09%; 95% confidence interval (CI) 43.78% to 44.39%). We found evidence for a genetic correlation between epilepsy and some neurodevelopmental and psychiatric conditions. For example, we observed a genetic correlation between epilepsy and attention-deficit/hyperactivity disorder (r(g)=0.18, 95% CI 0.09 to 0.27, p<0.001)-a correlation that was more pronounced in focal epilepsy (r(g)=0.23, 95% CI 0.09 to 0.36, p<0.001). Findings from Mendelian randomisation using common genetic variants did not support bidirectional effects between epilepsy and neurodevelopmental or psychiatric conditions. Conclusions Psychiatric comorbidities are common in patients with epilepsy. Genetic correlations may partially explain some comorbidities; however, there is little evidence of a bidirectional relationship between the genetic liability of epilepsy and psychiatric conditions. These findings highlight the need to understand the role of environmental factors or rare genetic variations in the origins of psychiatric comorbidities in epilepsy.
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