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Human CRY1 variants associate with attention deficit/hyperactivity disorder
- Source :
- Journal of Clinical Investigation, J Clin Invest
- Publication Year :
- 2020
- Publisher :
- American Society for Clinical Investigation, 2020.
-
Abstract
- Attention deficit/hyperactivity disorder (ADHD) is a common and heritable phenotype frequently accompanied by insomnia, anxiety, and depression. Here, using a reverse phenotyping approach, we report heterozygous coding variations in the core circadian clock gene cryptochrome 1 in 15 unrelated multigenerational families with combined ADHD and insomnia. The variants led to functional alterations in the circadian molecular rhythms, providing a mechanistic link to the behavioral symptoms. One variant, CRY1Δ11 c.1657+3A>C, is present in approximately 1% of Europeans, therefore standing out as a diagnostic and therapeutic marker. We showed by exome sequencing in an independent cohort of patients with combined ADHD and insomnia that 8 of 62 patients and 0 of 369 controls carried CRY1Δ11. Also, we identified a variant, CRY1Δ6 c.825+1G>A, that shows reduced affinity for BMAL1/CLOCK and causes an arrhythmic phenotype. Genotype-phenotype correlation analysis revealed that this variant segregated with ADHD and delayed sleep phase disorder (DSPD) in the affected family. Finally, we found in a phenome-wide association study involving 9438 unrelated adult Europeans that CRY1Δ11 was associated with major depressive disorder, insomnia, and anxiety. These results defined a distinctive group of circadian psychiatric phenotypes that we propose to designate as "circiatric" disorders.<br />NIH Clinical and Translational Science Award (CTSA) Program; NIH; French National Research Agency (ANR) under the “Investments for the future” Program; Integrative Biology of Emerging Infectious Diseases Laboratoire d’Excellence; IEIHSEER Grant; SEAe-Host Factors Grant; PNEUMOID Project Grant; INCA/Cancéropole Ile-de-France; Turkish Academy of Sciences (TÜBA); National Center for Advancing Translational Sciences (NCAST); Rockefeller University, INSERM; HHMI, University of Paris; St. Giles Foundation; Charles Bronfman Institute for Personalized Medicine at the Icahn School of Medicine at Mount Sinai
- Subjects :
- Adult
Male
0301 basic medicine
Genetic diseases
Genetics
Monogenic diseases
Psychiatric diseases
CLOCK Proteins
Delayed sleep phase
Bioinformatics
ARNTL Transcription Factors
Attention Deficit Disorder with Hyperactivity
Cryptochromes
Female
Genetic Association Studies
HEK293 Cells
Humans
Sleep Disorders, Circadian Rhythm
Mutation
03 medical and health sciences
0302 clinical medicine
mental disorders
Insomnia
Medicine
Attention deficit hyperactivity disorder
Circadian rhythm
Exome sequencing
Depression (differential diagnoses)
business.industry
General Medicine
medicine.disease
Circadian Rhythm
Biology
030104 developmental biology
030220 oncology & carcinogenesis
Anxiety
Major depressive disorder
medicine.symptom
Sleep Disorders
business
Research Article
Subjects
Details
- ISSN :
- 15588238 and 00219738
- Volume :
- 130
- Database :
- OpenAIRE
- Journal :
- Journal of Clinical Investigation
- Accession number :
- edsair.doi.dedup.....c26e34969651363455b6ea63aaffd9dd
- Full Text :
- https://doi.org/10.1172/jci135500