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Association of sunlight intensity with Attention-Deficit/Hyperactivity Disorder (ADHD) symptoms and interactions with pharmacological treatment: A cross-sectional approach.
Proposal
5513
Title of Proposed Research
Association of sunlight intensity with Attention-Deficit/Hyperactivity Disorder (ADHD) symptoms and interactions with pharmacological treatment: A cross-sectional approach.
Lead Researcher
Martijn Arns
Affiliation
Research Institute Brainclinics, Nijmegen, The NetherlandsUtrecht University, Dept. of Experimental Psychology, Utrecht, The Netherlands
Funding Source
Potential Conflicts of Interest
Data Sharing Agreement Date
17 September 2018
Lay Summary
In previous studies we have reported on an association between lower prevalence of ADHD in geographical areas with high sunlight intensity (e.g. California, Spain) relative to areas characterized by low sunlight intensity (e.g. New York, The Netherlands, Germany). A large proportion of ADHD patients have difficulties falling asleep, related to a delayed biological clock (circadian clock), and such sleep problems could worsen attention in ADHD patients. The protective effect of high sunlight intensity are thus hypothesized to be related to the effects of intense sunlight at daytime on the biological clock, whereby the late chronotype (delayed circadian phase) normalizes and less inattentive issues are observed. We have now replicated this effect in 5 different datasets, using a geographical case-control approach focused on ADHD diagnoses. However, this effect has not been demonstrated yet on the individual symptom level using a cross-sectional approach. The first objective of this proposal is to relate the level of sunlight intensity (based on geographical location and date) to baseline levels of inattention and impulsivity/hyperactivity. In addition, many medications could potentially interact with the circadian system, hence the second objective is to investigate the interactions between sunlight intensity (or change) and the pharmacological treatment conducted.
Study Data Provided
[{ "PostingID": 2001, "Title": "LILLY-B4Z-SB-LYDW", "Description": "A Randomized, Double-Blind Comparison of Atomoxetine versus Placebo in Children and Adolescents with Attention-Deficit/Hyperactivity Disorder and Comorbid Oppositional Defiant Disorder" },{ "PostingID": 2227, "Title": "LILLY-B4Z-US-LYCC", "Description": "Evaluation of Continuous Symptom Treatment of ADHD: A Placebo-Controlled Double-Blind Assessment of Morning-Dosed or Evening-Dosed Strattera" },{ "PostingID": 2228, "Title": "LILLY-B4Z-MC-HFBD", "Description": "A Randomized, Double-Blind Study of Tomoxetine Hydrochloride,
Methylphenidate Hydrochloride, and Placebo in Pediatric Outpatients with Attention Deficit/Hyperactivity Disorder" },{ "PostingID": 2229, "Title": "LILLY-B4Z-MC-HFBF", "Description": "Long-Term, Open-Label, Safety Study of Tomoxetine Hydrochloride in
Patients, 6 Years and Older" },{ "PostingID": 2230, "Title": "LILLY-B4Z-MC-HFBK", "Description": "A Randomized, Double-Blind Study of Tomoxetine Hydrochloride,
Methylphenidate Hydrochloride, and Placebo in Pediatric Outpatients with Attention-Deficit/Hyperactivity Disorder" },{ "PostingID": 2231, "Title": "LILLY-B4Z-MC-LYAA", "Description": "A Phase III Randomized, Double-Blind Comparison of Placebo and
Tomoxetine Hydrochloride in Adult Outpatients with DSM-IV Attention-Deficit/Hyperactivity Disorder." },{ "PostingID": 2232, "Title": "LILLY-B4Z-MC-LYAB", "Description": "A Phase III Open-Label Safety and Efficacy Study of Tomoxetine Hydrochloride in Outpatients with ADHD, Ages 6 to 18 Years" },{ "PostingID": 2233, "Title": "LILLY-B4Z-MC-LYAC", "Description": "A Phase 3 Randomized, Double-Blind, Placebo-Controlled Efficacy and Safety
Comparison of Fixed-Dose Ranges (mg/kg/day) of Tomoxetine with Placebo in Child and Adolescent Outpatients with ADHD, Aged 8 to 18 Years" },{ "PostingID": 2235, "Title": "LILLY-B4Z-MC-LYAO", "Description": "A Phase III Randomized, Double-Blind Comparison of Placebo and
Tomoxetine Hydrochloride in Adult Outpatients with DSM-IV Attention-
Deficit/Hyperactivity Disorder." },{ "PostingID": 2237, "Title": "LILLY-B4Z-MC-LYAS", "Description": "A Randomized, Double-Blind Study of Tomoxetine Hydrochloride and Placebo
in Pediatric Outpatients with Attention Deficit/Hyperactivity Disorder and
Comorbid Tic Disorders" },{ "PostingID": 2238, "Title": "LILLY-B4Z-MC-LYAT", "Description": "Efficacy, Tolerability, and Safety of Once-Daily Atomoxetine Hydrochloride versus Placebo in Children with Attention-Deficit/Hyperactivity Disorder" },{ "PostingID": 2239, "Title": "LILLY-B4Z-MC-LYBB", "Description": "A Phase 3 Open-Label Safety and Efficacy Study of Tomoxetine Hydrochloride in Pediatric Outpatients (6 to 18 Years) with ADHD" },{ "PostingID": 2241, "Title": "LILLY-B4Z-MC-LYDO", "Description": "Maintenance of Response After Open-Label Treatment With Atomoxetine Hydrochloride in Adult Outpatients With Attention-Deficit/Hyperactivity Disorder (ADHD): A Placebo-Controlled, Randomized Withdrawal Study" },{ "PostingID": 3504, "Title": "LILLY-B4Z-MC-LYAX", "Description": "A Randomized, Double-Blind, Placebo-Controlled Study of Atomoxetine Hydrochloride in Adolescents with Attention-Deficit/Hyperactivity Disorder and Comorbid Depressive Disorder" },{ "PostingID": 3736, "Title": "LILLY-B4Z-US-LYCW", "Description": "A Randomized, Double-Blind Comparison of Placebo and Atomoxetine Hydrochloride Given Once a Day in Adults with Attention-Deficit/Hyperactivity Disorder: with a Secondary Examination of Impact of Treatment on Family Functioning" },{ "PostingID": 3737, "Title": "LILLY-B4Z-JE-LYEE", "Description": "A Double-Blind Placebo-Controlled Asian Study of Atomoxetine Hydrochloride in the Treatment of Adult Patients with Attention-Deficit/Hyperactivity Disorder (ADHD)" },{ "PostingID": 3739, "Title": "LILLY-B4Z-US-LYCU", "Description": "Efficacy and Safety of Once-Daily Atomoxetine Hydrochloride in Adults with ADHD Over an Extended Period of Time (6 months): with A Brief Evaluation of Executive Cognition" },{ "PostingID": 3740, "Title": "LILLY-B4Z-MC-LYAW", "Description": "A Double-Blind, Placebo-Controlled Trial of Atomoxetine Hydrochloride to Evaluate Efficacy in the School Setting in Children Ages 8 to 12 Years with Attention-Deficit/Hyperactivity Disorder" },{ "PostingID": 3741, "Title": "LILLY-B4Z-US-LYBG", "Description": "A Randomized, Double-Blind, Placebo-Controlled Trial of Once Daily Atomoxetine Hydrochloride to Evaluate Efficacy in the Treatment of Attention-Deficit/Hyperactivity Disorder in Children Ages 6-12 with an Assessment of Evening Behavior" },{ "PostingID": 3860, "Title": "LILLY-B4Z-MC-LYBV", "Description": "A Double-Blind Study of Functional Outcomes With Atomoxetine-Hydrochloride and Placebo in Adult Outpatients With DSM-IV Attention-Deficit/Hyperactivity Disorder" },{ "PostingID": 4345, "Title": "LILLY-B4Z-US-LYDZ", "Description": "A Double-Blind Study of Atomoxetine Hydrochloride Versus Placebo for the Treatment of ADHD in Young Adults With an Assessment of Associated Functional Outcomes" },{ "PostingID": 4810, "Title": "NOVARTIS-CRIT124DUS02", "Description": "A multicenter, double-blind, randomized, placebo-controlled, crossover study evaluating the efficacy and safety of methylphenidate hydrocholoride in female adolescents diagnosed with attention deficit/hyperactivity disorder" },{ "PostingID": 5056, "Title": "LILLY-B4Z-EW-S006", "Description": "ADORE – Attention-Deficit Hyperactivity Disorder Observational Research in Europe" }]
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