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A study to examine the association between serum vitamin D levels and genetic variation of VDR and dopamine-specific genes in Attention Deficit Hyperactivity Disorder (ADHD)

VDR gene polymorphism and Dopaminergic and VDR gene expression in Attention Deficit Hyperactivity Disorder (ADHD) - ADHD- Attention Deficit Hyperactivity disorder

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/08/072003
Enrollment
100
Registered
2024-08-06
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: F902- Attention-deficit hyperactivity disorder, combined type

Interventions

Control Intervention1: NIL: NIL

Sponsors

Amrita Institute of Medical Sciences and Research Centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1A. Healthy children (Controls): Children with no current medical illness and family history of any major psychiatric disorder, especially ADHD as defined by ICD-10/ DSM-V. 1B. ADHD patients (Cases): Children diagnosed with ADHD by the paediatrician and the clinical psychologist using the Vanderbilt ADHD rating scale and who are on therapy or not. Comorbid with ODD, SLD, and CD will be included. 2. Willing to withdraw blood and participate in the study after giving consent. 3. Responsible caregiver to provide sufficient information about the participant’s functional status.

Exclusion criteria

Exclusion criteria: 1. History of any neurological disorder and psychiatric conditions involving the brain or other central function (eg: History of brain injury, suspected intellectual disability, autism spectrum disorder, narcolepsy, H/O mental retardation (MR), schizophrenia, mania episode, epilepsy, anxiety disorders, bipolar disorder, active suicidal ideation) 2. Use of Anticoagulants 3. Having any serious medical condition, including inflammatory bowel disease, history of cancer, kidney or liver disease, hyperthyroidism, glaucoma, diabetes or cardiovascular disorders, gallstones, bile duct obstruction, stomach ulcers, or excess stomach acid, abnormality of mineral metabolism eg: Wilson’s disease, hemochromatosis 4. Having any disability that would interfere with participation in the study.

Design outcomes

Primary

MeasureTime frame
Evaluation of serum Vitamin D levels will help to rule out the deficiency VDR gene polymorphism analysis will help to identify the alteration in the VDR gene that might affect the bioconversion of vitamin D in ADHDTimepoint: At the baseline visit alone, the blood samples will be collected. The serum will be separated for vitamin D estimation and DNA will be isolated for polymorphism analysis.

Secondary

MeasureTime frame
The expression analysis of dopamine-specific genes (TH,DRD4,SLC6A3) & VDR will help to elucidate molecular-level changes that will affect the pathophysiology of ADHD. The genomic analysis of these ADHD-specific genes can be used as an efficient biomarker for ADHD. It will help to improve the treatment outcome by individualizing the treatment modalities accordingly Timepoint: At the baseline visit alone, Blood samples will be collected & mRNA will be isolated

Countries

India

Contacts

Public ContactMintu Mathew

Amrita School of Pharmacy

jayamarythomas@gmail.com8851388785

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026