Ignite Creation Date:
2025-12-18 @ 8:12 AM
Ignite Modification Date:
2025-12-23 @ 6:57 PM
Study NCT ID:
NCT04860024
Status:
None
Last Update Posted:
2021-04-26 00:00:00
First Post:
2021-04-23 00:00:00
Is Possible Gene Therapy:
False
Has Adverse Events:
False
Brief Title:
Epigenetics in ADHD
Sponsor:
None
Organization:
Study Overview
Official Title:
The Prospective Role of Epigenetics in Attention-deficit/Hyperactivity Disorderdeficit/Hyperactivity Disorder
Status:
None
Status Verified Date:
2021-04
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Year 1: Recruiting 100 ADHD patients and 100 healthy control subjects (Training Set) to develop a miRNA diagnosis panel for ADHD
1\. One hundred eligible ADHD patients that are being treated in the Outpatient Department of Child Psychiatry at Kaohsiung Chang Gung Memorial Hospital in Taiwan will be recruited for this study. One hundred age- and gender-matched control subjects will be found in the same catchment area as that of the patients. After obtaining informed consent from their parents or guardians, research psychiatrists shall interview the participants using the K-SADS-E to confirm the diagnosis. The participants will also undergo WISC-IV assessment to exclude intellectual disabilities.
2\. For both the ADHD patients and the healthy control subjects, experienced child psychologists will administer Conners CPT and Conners CATA testing in a room designed to reduce inconsistent testing conditions. Parents or guardians will be required to complete the SNAP-IV parent form and the SAICA; patients' teachers will be required to fill out the SNAP-IV teacher form; and the ADHD-RS and the CGI will be completed and rated, respectively, by a child psychiatrist.
3\. Venous blood will be collected from each participant in an EDTA anticoagulant tube. The blood samples will be further processed with the mirVana miRNA isolation kit (Life technology) to extract total RNAs. Based on the preliminary findings, the ΔCt values of the 22 candidate miRNAs will be determined for the 100 ADHD samples and 100 control samples. Then the 10 miRNAs with the smallest p-value will be chosen to develop a miRNAs diagnosis panel for ADHD in the second year.
4\. The ADHD patients and healthy control subjects will have 12 months of follow-up. The treatment procedures during that time for patients with ADHD will be determined by the patients' psychiatrists' traditional practice and the agreement of patients and their parents.
1. ADHD patients who decide to receive medical treatment will be prescribed oral short-acting MPH (MPH-IR) two or three times daily, with each dose ranging between 0.3 and 1.0 mg/kg, which shall be determined based on the severity of their clinical symptoms, as well as their age, height, and body weight.
2. The dosage will be adjusted every two weeks to properly improve ADHD symptoms. Changes to long-acting MPH (Ritalin-LA) or extended-release methylphenidate (Concerta) are permitted depending on clinical requirements. The maximum doses of MPH-IR and Ritalin-LA per day are 60 mg and of Concerta is 54 mg, as these are the maximum daily doses approved in Taiwan. The dose will be decreased should any clinically intolerable adverse conditions arise. The final titration dose of MPH with an acceptable response will be maintained through the follow-up period.
3. Concomitant medications are prohibited. Compliance with the drug regimen will be verified at each visit based on reports by the patients' parents and how much of the prescription remains. Patients that start a new medication between the different time-points of the study will be considered dropouts.
4. The ADHD Patients that decide not to receive medical treatment are usually reassessed by a child psychiatrist in the outpatient department once a month and may receive behavioral therapy or re-educative psychotherapy for the duration of the study.
5. The healthy control subjects will be assessed only once, at the baseline. 5. Patients with ADHD will be reassessed at the twelfth month after baseline. The assessment procedures, including miRNAs analysis and ADHD measures, that were administered at baseline will be replicated.
Year 2: Developing a SVM classification model and enrolling an independent validation group with 50 ADHD patients and 50 healthy control subjects (Testing Set)
1. Based on the samples already gathered, the 10 most differentially expressed miRNAs between the ADHD group and control group can be determined. Those 10 values can be used to derive the SVM classification model and create a dependable and strong miRNA diagnosis panel for ADHD. Receiver operating characteristic (ROC) curves will be applied to evaluate the validity of this miRNA diagnosis panel. Both the specificity and sensitivity of this panel are expected to reach 80%.
2. For the independent validation group (Testing Set), 50 eligible patients with ADHD and 50 age- and gender-matched healthy control subjects will be recruited. Research psychiatrists will interview the participants using the K-SADS-E to confirm the diagnosis, and the participants will also undergo WISC-IV assessment to exclude intellectual disabilities.
3. All ADHD patients and healthy control subjects will have experienced child psychologists administer Conners' CPT and Conners' CATA testing. The parents or guardians of the participants are required to complete the SNAP-IV parent form and the SAICA; the patient' teachers are required to complete the SNAP-IV teacher form; and the ADHD-RS and the CGI will be completed and rated, respectively, by a child psychiatrist.
4. Venous blood will be collected from each participant using an EDTA anticoagulant tube. The blood samples will be further processed with the mirVana miRNA isolation kit (Life technology) to extract total RNAs. The levels of the 10 miRNAs elected for the SVM classification model will be determined by qRT-PCR.
5. To verify the results of the Training Set, the miRNAs data of the Testing Set (both the 50 ADHD patients and the 50 healthy control subjects) will be used for blind testing by the miRNA diagnosis panel. The discrimination validity expects both the sensitivity and specificity to reach 80%.
6. The treatment and follow-up procedure for ADHD patients will be the same as in the first year. The 100 ADHD patients recruited in the first year will be followed and reevaluated
Year 3: Completion of the 12-month follow-up of ADHD patients and performing analysis of target genes and enrichment pathways of the miRNAs
1. No new participants will be recruited in the third year. The 12-month follow-up of all 150 patients with ADHD will be completed during this year.
2. The second assessment of patients with ADHD will be carried out to conclude this study (twelfth month after baseline). The same assessment procedures that were administered at baseline will be replicated.
(1) Blood samples will be collected and be processed again to extract miRNAs-. (2) A research psychiatrist will interview the ADHD patients using the K-SADS-E in order to confirm that the patients still meet the diagnostic criteria of ADHD.
(3) Patients with ADHD will undergo neuropsychological testing (WISC-IV, Conners CPT and Conners CATA) and have their behavioral symptoms rated (SNAP-IV, SAICA, ADHD-RS and CGI) by the same rater at baseline. To avoid any bias derived from medication, ADHD patients will be told not to take their medication on the day of the neuropsychological assessment.
3\. The trends of the miRNA levels during the 12-month follow-up will be identified. The differential miRNA levels between patients with versus without MPH treatment and between patients who continue versus those who remit from the ADHD diagnosis will be evaluated. Whether miRNAs can function as a biomarker that portrays the ADHD condition after treatment will be determined.
4\. The predicted target genes and their enrichment pathways of the differentially expressed miRNAs will be obtained using TargetScan v6.2, miRWalk, and DIANA-microT. The search will focus exclusively on the 3'-UTR regions of the target miRNAs with a p-value of 0.05 defining the probability distribution of random matches set in the software with a minimum miRNA seed length of 7.
1\. One hundred eligible ADHD patients that are being treated in the Outpatient Department of Child Psychiatry at Kaohsiung Chang Gung Memorial Hospital in Taiwan will be recruited for this study. One hundred age- and gender-matched control subjects will be found in the same catchment area as that of the patients. After obtaining informed consent from their parents or guardians, research psychiatrists shall interview the participants using the K-SADS-E to confirm the diagnosis. The participants will also undergo WISC-IV assessment to exclude intellectual disabilities.
2\. For both the ADHD patients and the healthy control subjects, experienced child psychologists will administer Conners CPT and Conners CATA testing in a room designed to reduce inconsistent testing conditions. Parents or guardians will be required to complete the SNAP-IV parent form and the SAICA; patients' teachers will be required to fill out the SNAP-IV teacher form; and the ADHD-RS and the CGI will be completed and rated, respectively, by a child psychiatrist.
3\. Venous blood will be collected from each participant in an EDTA anticoagulant tube. The blood samples will be further processed with the mirVana miRNA isolation kit (Life technology) to extract total RNAs. Based on the preliminary findings, the ΔCt values of the 22 candidate miRNAs will be determined for the 100 ADHD samples and 100 control samples. Then the 10 miRNAs with the smallest p-value will be chosen to develop a miRNAs diagnosis panel for ADHD in the second year.
4\. The ADHD patients and healthy control subjects will have 12 months of follow-up. The treatment procedures during that time for patients with ADHD will be determined by the patients' psychiatrists' traditional practice and the agreement of patients and their parents.
1. ADHD patients who decide to receive medical treatment will be prescribed oral short-acting MPH (MPH-IR) two or three times daily, with each dose ranging between 0.3 and 1.0 mg/kg, which shall be determined based on the severity of their clinical symptoms, as well as their age, height, and body weight.
2. The dosage will be adjusted every two weeks to properly improve ADHD symptoms. Changes to long-acting MPH (Ritalin-LA) or extended-release methylphenidate (Concerta) are permitted depending on clinical requirements. The maximum doses of MPH-IR and Ritalin-LA per day are 60 mg and of Concerta is 54 mg, as these are the maximum daily doses approved in Taiwan. The dose will be decreased should any clinically intolerable adverse conditions arise. The final titration dose of MPH with an acceptable response will be maintained through the follow-up period.
3. Concomitant medications are prohibited. Compliance with the drug regimen will be verified at each visit based on reports by the patients' parents and how much of the prescription remains. Patients that start a new medication between the different time-points of the study will be considered dropouts.
4. The ADHD Patients that decide not to receive medical treatment are usually reassessed by a child psychiatrist in the outpatient department once a month and may receive behavioral therapy or re-educative psychotherapy for the duration of the study.
5. The healthy control subjects will be assessed only once, at the baseline. 5. Patients with ADHD will be reassessed at the twelfth month after baseline. The assessment procedures, including miRNAs analysis and ADHD measures, that were administered at baseline will be replicated.
Year 2: Developing a SVM classification model and enrolling an independent validation group with 50 ADHD patients and 50 healthy control subjects (Testing Set)
1. Based on the samples already gathered, the 10 most differentially expressed miRNAs between the ADHD group and control group can be determined. Those 10 values can be used to derive the SVM classification model and create a dependable and strong miRNA diagnosis panel for ADHD. Receiver operating characteristic (ROC) curves will be applied to evaluate the validity of this miRNA diagnosis panel. Both the specificity and sensitivity of this panel are expected to reach 80%.
2. For the independent validation group (Testing Set), 50 eligible patients with ADHD and 50 age- and gender-matched healthy control subjects will be recruited. Research psychiatrists will interview the participants using the K-SADS-E to confirm the diagnosis, and the participants will also undergo WISC-IV assessment to exclude intellectual disabilities.
3. All ADHD patients and healthy control subjects will have experienced child psychologists administer Conners' CPT and Conners' CATA testing. The parents or guardians of the participants are required to complete the SNAP-IV parent form and the SAICA; the patient' teachers are required to complete the SNAP-IV teacher form; and the ADHD-RS and the CGI will be completed and rated, respectively, by a child psychiatrist.
4. Venous blood will be collected from each participant using an EDTA anticoagulant tube. The blood samples will be further processed with the mirVana miRNA isolation kit (Life technology) to extract total RNAs. The levels of the 10 miRNAs elected for the SVM classification model will be determined by qRT-PCR.
5. To verify the results of the Training Set, the miRNAs data of the Testing Set (both the 50 ADHD patients and the 50 healthy control subjects) will be used for blind testing by the miRNA diagnosis panel. The discrimination validity expects both the sensitivity and specificity to reach 80%.
6. The treatment and follow-up procedure for ADHD patients will be the same as in the first year. The 100 ADHD patients recruited in the first year will be followed and reevaluated
Year 3: Completion of the 12-month follow-up of ADHD patients and performing analysis of target genes and enrichment pathways of the miRNAs
1. No new participants will be recruited in the third year. The 12-month follow-up of all 150 patients with ADHD will be completed during this year.
2. The second assessment of patients with ADHD will be carried out to conclude this study (twelfth month after baseline). The same assessment procedures that were administered at baseline will be replicated.
(1) Blood samples will be collected and be processed again to extract miRNAs-. (2) A research psychiatrist will interview the ADHD patients using the K-SADS-E in order to confirm that the patients still meet the diagnostic criteria of ADHD.
(3) Patients with ADHD will undergo neuropsychological testing (WISC-IV, Conners CPT and Conners CATA) and have their behavioral symptoms rated (SNAP-IV, SAICA, ADHD-RS and CGI) by the same rater at baseline. To avoid any bias derived from medication, ADHD patients will be told not to take their medication on the day of the neuropsychological assessment.
3\. The trends of the miRNA levels during the 12-month follow-up will be identified. The differential miRNA levels between patients with versus without MPH treatment and between patients who continue versus those who remit from the ADHD diagnosis will be evaluated. Whether miRNAs can function as a biomarker that portrays the ADHD condition after treatment will be determined.
4\. The predicted target genes and their enrichment pathways of the differentially expressed miRNAs will be obtained using TargetScan v6.2, miRWalk, and DIANA-microT. The search will focus exclusively on the 3'-UTR regions of the target miRNAs with a p-value of 0.05 defining the probability distribution of random matches set in the software with a minimum miRNA seed length of 7.
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?: