Coenzyme Q10, Vitamin E and Polyvitamin B: an exploratory double-blind randomized cross-over study in Phelan-McDermid Syndrome

Antonio M. Persico , Arianna Ricciardello , Francesca Cucinotta , Laura Turriziani , Giorgia Calabrese , Pasquale Tomaiuolo , Tiziana Di Bella , Fabiana Bellomo , Maria Boncoddo , Giada Turturo , Silvestro Mirabelli , Lisa Asta , Federico Banchelli , Riccardo Cuoghi Costantini , Roberto D'Amico

Rare Disease and Orphan Drugs Journal ›› 2023, Vol. 2 ›› Issue (3) : 13

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Rare Disease and Orphan Drugs Journal ›› 2023, Vol. 2 ›› Issue (3) :13 DOI: 10.20517/rdodj.2023.08
Original Article

Coenzyme Q10, Vitamin E and Polyvitamin B: an exploratory double-blind randomized cross-over study in Phelan-McDermid Syndrome

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Abstract

Aim: Defective mitochondrial function and increased oxidative stress have been documented in Autism Spectrum Disorder (ASD) and Phelan-McDermid syndrome (PMS), one of the best-known monogenic forms of ASD. The purpose of this exploratory, double-blind, randomized cross-over trial (RCT) is to verify the efficacy and safety of a “metabolic support therapy” (MST) in PMS, while defining the experimental methodology most apt at maximizing sensitivity and reliability.

Methods: A total of 31 PMS patients completed 4 months of Coenzyme Q10 (50/100 mg b.i.d.) + vitamin E (30/60 mg/d) + polyvitamin B ("active compound") vs. 4 months of only Vitamins E and B ("active comparator"). To explore their sensitivity and reliability, four primary outcome measures were used: VABS, CARS, CGI-I, and VAS. Secondary outcome measures span adaptive behaviors, social cognition, autism, problem behaviors, quality of life (QoL), communication, and comorbidities.

Results: CoQ10+vit. E and B yielded significantly greater improvement in several measures of cognition and adaptive functioning, motor skills, and stereotypic behaviors compared to vit. E and B only. Maternal QoL was especially improved in the presence of CoQ10 (P < 0.004). Time x Treatment interactions in CGI-I and VAS "restricted interests" scores support positive contributions also by vitamins E and B. Side effects, including hyperactivity, insomnia, and irritability, were mild, rare, and did not differ between treatment periods.

Conclusion: MST may produce small-to-moderate improvement, especially in motor skills, social motivation, adaptive behaviors, responsiveness to environmental stimulation, and stereotypic behaviors in up to approximately 70% of PMS patients. A targeted confirmatory RCT contrasting Q10+vit E and B vs. inactive placebo is now warranted.

Keywords

22q13 deletion syndrome / autism / autism spectrum disorder / coenzyme Q10 / Phelan-McDermid syndrome / SHANK3 / vitamin B / vitamin E.

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Antonio M. Persico, Arianna Ricciardello, Francesca Cucinotta, Laura Turriziani, Giorgia Calabrese, Pasquale Tomaiuolo, Tiziana Di Bella, Fabiana Bellomo, Maria Boncoddo, Giada Turturo, Silvestro Mirabelli, Lisa Asta, Federico Banchelli, Riccardo Cuoghi Costantini, Roberto D'Amico. Coenzyme Q10, Vitamin E and Polyvitamin B: an exploratory double-blind randomized cross-over study in Phelan-McDermid Syndrome. Rare Disease and Orphan Drugs Journal, 2023, 2(3): 13 DOI:10.20517/rdodj.2023.08

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References

[1]

Phelan MC,Saul RA.22q13 deletion syndrome.Am J Med Genet2001;101:91-9

[2]

Phelan K,Boccuto L. Phelan-McDermid syndrome. In M. P. Adam (Eds.) et. al., GeneReviews®. University of Washington, Seattle; 2005. Available from: https://www.ncbi.nlm.nih.gov/books/NBK1198/[Last accessed on 10 Jul 2023]

[3]

Phelan K.The 22q13.3 deletion syndrome (Phelan-McDermid Syndrome).Mol Syndromol2012;2:186-201 PMCID:PMC3366702

[4]

Kolevzon A,Bush L.Phelan-McDermid syndrome: a review of the literature and practice parameters for medical assessment and monitoring.J Neurodev Disord2014;6:39 PMCID:PMC4362650

[5]

National Organization for Rare Disorders. Phelan-cDermid sndrome. Available from: https://rarediseases.org/rare-diseases/phelan-mcdermid-syndrome/#affected-populations [Last accessed on 7 Jul 2023]

[6]

Betancur C.SHANK3 haploinsufficiency: a "common" but underdiagnosed highly penetrant monogenic cause of autism spectrum disorders.Mol Autism2013;4:17. PMCID:PMC3695795

[7]

Soorya L,Zweifach J.Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiency.Mol Autism2013;4:18 PMCID:PMC3707861

[8]

Sarasua SM,Sharp JL.Clinical and genomic evaluation of 201 patients with Phelan-McDermid syndrome.Hum Genet2014;133:847-59

[9]

Kohlenberg TM,McLarney B,Thurm A.Psychiatric illness and regression in individuals with Phelan-McDermid syndrome.J Neurodev Disord2020;12:7 PMCID:PMC7014655

[10]

Kolevzon A,Berry-Kravis E,Betancur C.Neuropsychiatric decompensation in adolescents and adults with Phelan-McDermid syndrome: a systematic review of the literature.Mol Autism2019;10:50 PMCID:PMC6930682

[11]

De Rubeis S,Durkin A.Delineation of the genetic and clinical spectrum of Phelan-McDermid syndrome caused by SHANK3 point mutations.Mol Autism2018;9:31 PMCID:PMC5921983

[12]

Disciglio V,Mencarelli MA.Interstitial 22q13 deletions not involving SHANK3 gene: a new contiguous gene syndrome.Am J Med Genet A2014;164A:1666-76

[13]

Ricciardello A,Persico AM.Genotype-phenotype correlation in Phelan-McDermid syndrome: A comprehensive review of chromosome 22q13 deleted genes.Am J Med Genet A2021;185:2211-33 PMCID:PMC8251815

[14]

Vondráčková A,Kratochvílová H.Large copy number variations in combination with point mutations in the TYMP and SCO2 genes found in two patients with mitochondrial disorders.Eur J Hum Genet2014;22:431-4 PMCID:PMC3925276

[15]

Frye RE.Mitochondrial disease in 22q13 duplication syndrome.J Child Neurol2012;27:942-9

[16]

Costales JL.Phelan-McDermid sndrome and SHANK3: iplications for teatment.Neurotherapeutics2015;12:620-30 PMCID:PMC4489957

[17]

Verhoeven WMA,de Leeuw N.A longitudinal perspective on the pharmacotherapy of 24 adult patients with Phelan-McDermid syndrome.Eur J Med Genet2020;63:103751

[18]

Wang Y.Understanding ubiquinone.Trends Cell Biol2016;26:367-78.

[19]

Mantle D.Bioavailability of cenzyme Q(10): an overview of the absorption process and subsequent metabolism.Antioxidants2020;9:386. PMCID:PMC7278738

[20]

Weber C,Hłlmer G.The coenzyme Q10 content of the average Danish diet.Int J Vitam Nutr Res1997;67:123-9

[21]

Hargreaves IP.Coenzyme Q10 as a therapy for mitochondrial disease.Int J Biochem Cell Biol2014;49:105e111

[22]

Matthews RT,Browne S,Beal MF.Coenzyme Q10 administration increases brain mitochondrial concentrations and exerts neuroprotective effects.Proc Natl Acad Sci USA1998;95:8892-7 PMCID:PMC21173

[23]

Rötig A,Geromel V.Quinone-responsive multiple respiratory-chain dysfunction due to widespread coenzyme Q10 deficiency.Lancet2000;356:391-5

[24]

Beal MF.Mitochondrial dysfunction and oxidative damage in Alzheimer's and Parkinson's diseases and coenzyme Q10 as a potential treatment.J Bioenerg Biomembr2004;36:381-6

[25]

Papucci L,Witort E.Coenzyme q10 prevents apoptosis by inhibiting mitochondrial depolarization independently of its free radical scavenging property.J Biol Chem2003;278:28220-8

[26]

Kalayci M,Gul S.Effect of coenzyme Q10 on ischemia and neuronal damage in an experimental traumatic brain-injury model in rats.BMC Neuroscience2011;12:75 PMCID:PMC3160960

[27]

Kumari S,Milledge GZ,Li H.Ubisol-Q10 prevents glutamate-induced cell death by blocking mitochondrial fragmentation and permeability transition pore opening.Int J Biol Sci2016; 12:688-700. PMCID:PMC4870712

[28]

Degenhardt F,Szymczak S.Genome-wide association study of serum coenzyme Q10 levels identifies susceptibility loci linked to neuronal diseases.Hum Mol Genet2016;25:2881-91

[29]

Somayajulu M,Hung M,Borowy-Borowski H.Role of mitochondria in neuronal cell death induced by oxidative stress; neuroprotection by Coenzyme Q10.Neurobiol Dis2005;18:618-27

[30]

Moon Y,Park JH,Kim K.Mitochondrial membrane depolarization and the selective death of dopaminergic neurons by rotenone: protective effect of coenzyme Q10.J Neurochem2005;93:1199-208

[31]

Hochberg J.Latissimus dorsi myocutaneous flap to restore elbow flexion and axillary burn contracture: a report on two pediatric patients.J Pediatr Orthop1982;2:565-8

[32]

Müller T,Gholipour AF.Coenzyme Q10 supplementation provides mild symptomatic benefit in patients with Parkinson's disease.Neurosci Lett2003;341:201-4

[33]

Shults CW,Fontaine D,Haas RH.Absorption, tolerability, and effects on mitochondrial activity of oral coenzyme Q10 in parkinsonian patients.Neurology1998;50:793-5

[34]

Cooper O,Andrabi S.Pharmacological rescue of mitochondrial deficits in iPSC-derived neural cells from patients with familial Parkinson's disease.Sci Transl Med2012;4:141ra90 PMCID:PMC3462009

[35]

Cucinotta F,Turriziani L.Efficacy and safety of Q10 ubiquinol with vitamins b and e in neurodevelopmental disorders: a retrospective chart review.Front Psychiatry2022;13:829516 PMCID:PMC8927903

[36]

Psychiatric Association. Diagnostic and statistical manual of mental disorders.Med Health Care Phil2014;17:241-244.

[37]

Soorya L,Trelles MP.Framework for assessing individuals with rare genetic disorders associated with profound intellectual and multiple disabilities (PIMD): the example of Phelan McDermid Syndrome.Clin Neuropsychol2018;32:1226-55 PMCID:PMC6417924

[38]

Braconnier ML.Neuropsychological assessment in autism spectrum disorder.Curr Psychiatry Rep2021;23:63 PMCID:PMC8324442

[39]

Jacquemont S,Hagerman R.The challenges of clinical trials in fragile X syndrome.Psychopharmacology2014;231:1237-50 PMCID:PMC3932172

[40]

Sparrow SS,Balla DA. Vineland adaptive behavior scales: second edition (Vineland II), survey interview form/caregiver rating form. Livonia, MN: Pearson Assessments; 2005. Available from: https://www.walmart.com/ip/Vineland-II-Vineland-Adaptive-Behavior-Scales-Survey-Forms-Manual-Interview-Form-Parent-Caregiver-Rating-Form-Pre-Owned-Unknown-Binding-B001P673SK-Do/702415787 [Last accessed on 7 Jul 2023]

[41]

Vaughan CA.Test Review: E. Schopler, M. E. Van Bourgondien, G. J. Wellman, & S. R. Love Childhood Autism Rating Scale (2nd ed.). Los Angeles, CA: Western Psychological Services, 2010..J Psychoeduc Assess2011;29:489-93

[42]

Guy W. Clinical global impressions ECDEU assessment manual for psychopharmacology. Rockville, MD: National Institute for Mental Health; 1976. Available from: https://ia600306.us.archive.org/35/items/ecdeuassessmentm1933guyw/ecdeuassessmentm1933guyw.pdf [Last accessed on 7 Jul 2023]

[43]

Guyatt GH,Berman LB.A comparison of likert and visual analogue scales for measuring change in function.J Chronic Dis1987;40:1129-33

[44]

Jaeschke R,Guyatt GH.A comparison of seven-point and visual analogue scales. Data from a randomized trial.Control Clin Trials1990;11:43-51

[45]

Shaffer D,Brasic J.A children's global assessment scale (CGAS).Arch Gen Psychiatry1983;40:1228-31

[46]

Constantino JN,Todd RD.Validation of a brief quantitative measure of autistic traits: comparison of the social responsiveness scale with the autism diagnostic interview-revised.J Autism Dev Disord2003;33:427-33

[47]

Lam KS. The repetitive behavior scale-revised: independent validation in individuals with autism spectrum disorders.J Autism Dev Disord2007;37:855-66

[48]

Aman MG,Stewart AW.The aberrant behavior checklist: a behavior rating scale for the assessment of treatment effects.Am J Ment Defic1985;89:485-91. PMID: 3993694

[49]

Tomchek SD.Sensory processing in children with and without autism: a comparative study using the short sensory profile.Am J Occup Ther2007;61:190-200

[50]

Conners CK,Parker JD.The revised Conners' Parent Rating Scale (CPRS-R): factor structure, reliability, and criterion validity.J Abnorm Child Psychol1998;26:257-68

[51]

Achenbach TM. Manual for the ASEBA preschool forms and profiles. Burlington, VT: University of Vermont, Research Center for Children, Youth, and Families; 2000. Available from: https://www.researchgate.net/publication/243771256_Manual_for_the_ASEBA_Preschool_forms_profiles [Last accessed on 7 Jul 2023]

[52]

Achenbach TM. Manual for the ASEBA school-age forms and profiles. Burlington, VT: University of Vermont, Research Center for Children, Youth, and Families; 2001. Available from: https://store.aseba.org/MANUAL-FOR-THE-ASEBA-SCHOOL-AGE-FORMS-PROFILES/productinfo/505/ [Last accessed on 7 Jul2023]

[53]

McConachie H,Parr JR,Wilson C.Enhancing the validity of a quality of life measure for autistic people.J Autism Dev Disord2018;48:1596-611 PMCID:PMC5889785

[54]

The WHOQOL GroupDevelopment of the World Health Organization WHOQOL-BREF quality of life assessment.Psychol Med1998;28:551-8

[55]

R Core Team. R: A language and environment for statistical computing. R Foundation for Statistical Computing, Wien, Austria; 2020.

[56]

Ponson L,Blanc R.22q13 deletion syndrome: communication disorder or autism?.Transl Psychiatry2018;8:146 PMCID:PMC6082846

[57]

Kann O.Mitochondria and neuronal activity.Am J Physiol Cell Physiol2007;292:C641-57

[58]

Cheng A,Mattson MP.Mitochondria and neuroplasticity.ASN Neuro2010;2:e00045 PMCID:PMC2949087

[59]

Carmeli E,Bachar A.Inflammation and oxidative stress as biomarkers of premature aging in persons with intellectual disability.Res Dev Disabil2012;33:369-75

[60]

Valenti D,De Filippis B,Vacca RA.Mitochondrial dysfunction as a central actor in intellectual disability-related diseases: an overview of Down syndrome, autism, Fragile X and Rett syndrome.Neurosci Biobehav Rev2014;46 Pt 2:202-17

[61]

Alvarez-Mora MI,Madrigal I,Garrabou G.Impaired mitochondrial function and dynamics in the pathogenesis of FXTAS.Mol Neurobiol2017;54:6896-902

[62]

Liu J,Zhan S,Wang L.Coenzyme Q10 for Parkinson's disease. cochrane database of systematic reviews.1996;

[63]

Persico AM,Ricciardello A.Autisms. Neurodevelopmental disorders. Elsevier; 2020. pp. 35-77.

[64]

Rossignol DA.Evidence linking oxidative stress, mitochondrial dysfunction, and inflammation in the brain of individuals with autism.Front Physiol2014; 5:150. PMCID:PMC4001006

[65]

Palmieri L.Mitochondrial dysfunction in autism spectrum disorders: cause or effect?.Biochim Biophys Acta2010; 1797:1130-7

[66]

Palmieri L,Porcelli V.Altered calcium homeostasis in autism-spectrum disorders: evidence from biochemical and genetic studies of the mitochondrial aspartate/glutamate carrier AGC1.Mol Psychiatry2010; 15:38-52.

[67]

Chauhan A,Chauhan V.Brain region-specific glutathione redox imbalance in autism.Neurochem Res2012; 37:1681-9.

[68]

Rose S,Pavliv O.Evidence of oxidative damage and inflammation associated with low glutathione redox status in the autism brain.Transl Psychiatry2012; 2:e134. PMCID:PMC3410618

[69]

Frustaci A,Cesario A.Oxidative stress-related biomarkers in autism: systematic review and meta-analyses.Free Radic Biol Med2012; 52:2128-41.

[70]

Tang G,Kuo SH.Mitochondrial abnormalities in temporal lobe of autistic brain.Neurobiol Dis2013; 54:349-61 PMCID:PMC3959772

[71]

Gu F,Chauhan A.Impaired synthesis and antioxidant defense of glutathione in the cerebellum of autistic subjects: alterations in the activities and protein expression of glutathione-related enzymes.Free Radic Biol Med2013; 65:488-96.

[72]

El-Ansary A,Chirumbolo S.Predictive value of selected biomarkers related to metabolism and oxidative stress in children with autism spectrum disorder.Metab Brain Dis2017; 32:1209-21.

[73]

Yenkoyan K,Harutyunyan A.A certain role of SOD/CAT imbalance in pathogenesis of autism spectrum disorders.Free Radic Biol Med2018; 123:85-95.

[74]

Adams JB,Geis E.The severity of autism is associated with toxic metal body burden and red blood cell glutathione levels.J Toxicol2009; 2009:532640. PMCID:PMC2809421

[75]

Ghezzo A,Abruzzo PM.Oxidative stress and erythrocyte membrane alterations in children with autism: correlation with clinical features.PLoS One2013;8:e66418 PMCID:PMC3686873

[76]

Gorrindo P,Lee EB,Levitt P.Enrichment of elevated plasma F2t-isoprostane levels in individuals with autism who are stratified by presence of gastrointestinal dysfunction.PLoS One2013;8:e68444 PMCID:PMC3700867

[77]

Rose S,Murray KF,Winter H.Mitochondrial dysfunction in the gastrointestinal mucosa of children with autism: a blinded case-control study.PLoS One2017;12:e0186377. PMCID:PMC5640251

[78]

McElhanon BO,Karpen S.Gastrointestinal symptoms in autism spectrum disorder: a meta-analysis.Pediatrics2014;133:872-83.

[79]

Frye RE,Slattery J.Mitochondrial dysfunction may explain symptom variation in phelan-mcdermid syndrome.Sci Rep2016;6:19544 PMCID:PMC4731780

[80]

Naviaux RK.Oxidative shielding or oxidative stress?.J Pharmacol Exp Ther2012;342:608-18

[81]

Adams JB.Pilot study of a moderate dose multivitamin/mineral supplement for children with autistic spectrum disorder.J Altern Complement Med2004;10:1033-9

[82]

Adams JB,McDonough-Means S.Effect of a vitamin/mineral supplement on children and adults with autism.BMC Pediatr2011;11:111. PMCID:PMC3266205

[83]

Adams JB,Geis E.Comprehensive nutritional and dietary intervention for autism spectrum disorder-a randomized, controlled 12-month trial.Nutrients2018;10:369 PMCID:PMC6566397

[84]

Dolske MC,McKay S,Tolbert L.A preliminary trial of ascorbic acid as supplemental therapy for autism.Prog Neuropsych Biol Psychiatry1993;17:765-74

[85]

Adams JB,Audhya T.Abnormally high plasma levels of vitamin B6 in children with autism not taking supplements compared to controls not taking supplements.J Altern Complement Med2006;12:59-63

[86]

Mousavinejad E,Riahi F,Tiznobeyk Z.Coenzyme Q(10) supplementation reduces oxidative stress and decreases antioxidant enzyme activity in children with autism spectrum disorders.Psychiatry Res2018;265:62-9

[87]

Eldridge SM,Campbell MJ.PAFS consensus groupCONSORT 2010 statement: extension to randomised pilot and feasibility trials.Pilot Feasibility Stud2016;2:64 PMCID:PMC5154046

[88]

Matuleviciene A,Kuiper E.European Phelan-McDermid syndrome guideline consortiumConsensus recommendations on chewing, swallowing and gastrointestinal problems in Phelan-McDermid syndrome.Eur J Med Genet2023;66:104763

[89]

Serrada-Tejeda S,Máximo-Bocanegra N,Pérez-de-Heredia-Torres M.Descriptive analysis of adaptive behavior in Phelan-McDermid syndrome and autism spectrum disorder.Front Neurosci2022;16:893003 PMCID:PMC9295709

[90]

Droogmans G,Van Buggenhout G.Stressed parents, happy parents. An assessment of parenting stress and family quality of life in families with a child with Phelan-McDermid syndrome.J Appl Res Intellect Disabil2021;34:1076-88.

[91]

Jacob S,Hollander E.Large multicenter randomized trials in autism: key insights gained from the balovaptan clinical development program.Mol Autism2022;13:25 PMCID:PMC9188723

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