16 results on '"D'Onofrio, Gianluca"'
Search Results
2. Lithium Toxicity in Lepidium sativum L. Seedlings: Exploring Li Accumulation's Impact on Germination, Root Growth, and DNA Integrity.
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Iannilli, Valentina, D'Onofrio, Gianluca, Marzi, Davide, Passatore, Laura, Pietrini, Fabrizio, Massimi, Lorenzo, and Zacchini, Massimo
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ROOT growth ,LEPIDIUM ,GERMINATION ,SEEDLINGS ,NUCLEIC acids ,GENETIC toxicology ,LEMNA minor ,DNA damage - Abstract
The predicted increase in demand for minor metals for modern technologies raises major concerns regarding potential environmental concentration increases. Among the minor metals, lithium (Li) is particularly noteworthy due to growing demand for battery production. Concerns have been raised about the impact on biota of increasing Li concentrations in the environment. To expand the knowledge of the effects of Li on plants, garden cress (Lepidium sativum L.), a model plant for ecotoxicity assay, was tested in a 72 h test in Petri plates. The results showed a stimulation effect of Li at the lowest concentration (Li chloride 10 mg L
−1 ) on seed germination and primary root elongation. Conversely, higher Li concentrations (50 and 150 mg L−1 ) caused a progressive impairment in both parameters. A genotoxic effect of Li on root cells, evaluated through the alkaline comet assay, was observed at each concentration tested, particularly at 150 mg L−1 Li chloride. Elemental analysis showed that Li accumulated in the seedlings in a dose–concentration relationship, confirming its ability to be readily absorbed and accumulated in plants. Given the likely increase in Li levels in the environment, further research is required to clarify the toxicity mechanisms induced by Li on growth and nucleic acids. [ABSTRACT FROM AUTHOR]- Published
- 2024
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3. Myoclonus: Differential diagnosis and current management.
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Riva, Antonella, D'Onofrio, Gianluca, Ferlazzo, Edoardo, Pascarella, Angelo, Pasini, Elena, Franceschetti, Silvana, Panzica, Ferruccio, Canafoglia, Laura, Vignoli, Aglaia, Coppola, Antonietta, Badioni, Valeria, Beccaria, Francesca, Labate, Angelo, Gambardella, Antonio, Romeo, Antonino, Capovilla, Giuseppe, Michelucci, Roberto, Striano, Pasquale, and Belcastro, Vincenzo
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Myoclonus classically presents as a brief (10–50 ms duration), non‐rhythmic jerk movement. The etiology could vary considerably ranging from self‐limited to chronic or even progressive disorders, the latter falling into encephalopathic pictures that need a prompt diagnosis. Beyond the etiological classification, others evaluate myoclonus' body distribution (i.e., clinical classification) or the location of the generator (i.e., neurophysiological classification); particularly, knowing the anatomical source of myoclonus gives inputs on the observable clinical patterns, such as EMG bursts duration or EEG correlate, and guides the therapeutic choices. Among all the chronic disorders, myoclonus often presents itself as a manifestation of epilepsy. In this context, myoclonus has many facets. Myoclonus occurs as one, or the only, seizure manifestation while it can also present as a peculiar type of movement disorder; moreover, its electroclinical features within specific genetically determined epileptic syndromes have seldom been investigated. In this review, following a meeting of recognized experts, we provide an up‐to‐date overview of the neurophysiology and nosology surrounding myoclonus. Through the dedicated exploration of epileptic syndromes, coupled with pragmatic guidance, we aim to furnish clinicians and researchers alike with practical advice for heightened diagnostic management and refined treatment strategies. Plain Language Summary: In this work, we described myoclonus, a movement characterized by brief, shock‐like jerks. Myoclonus could be present in different diseases and its correct diagnosis helps treatment. [ABSTRACT FROM AUTHOR]
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- 2024
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4. A proposal for a shared therapeutic algorithm in children with prolonged convulsive seizures and status epilepticus.
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Roberti, Roberta, Riva, Antonella, D'Onofrio, Gianluca, Giacheri, Emanuele, Amadori, Elisabetta, Vari, Maria Stella, La Neve, Angela, Vigevano, Federico, Verrotti, Alberto, Cordelli, Duccio Maria, Romeo, Antonino, Palmieri, Antonella, Mancardi, Maria Margherita, Caglieris, Sergio, Varone, Antonio, Minetti, Carlo, Russo, Emilio, Buratti, Silvia, and Striano, Pasquale
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- 2024
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5. A European pilot study in Dravet Syndrome to delineate what really matters for the patients and families.
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Chemaly, Nicole, Kuchenbuch, Mathieu, Teng, Théo, Marie, Elodie, D'Onofrio, Gianluca, Lo Barco, Tommaso, Brambilla, Isabella, Flege, Silke, Hallet, Anne‐Sophie, and Nabbout, Rima
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PATIENTS' families ,PILOT projects ,PATIENT advocacy ,PRESSURE groups ,PEOPLE with epilepsy - Abstract
We aimed to identify caregivers' opinions on the outcome measures that matter in clinical trials in individuals with Dravet syndrome (DS). We conducted a prospective European multicenter study based on an 11 closed questions survey developed by the French reference center for rare epilepsies and DS patients' advocacy groups. Items included questions on seizures and daily life outcomes that a clinical trial on a therapy for individuals with DS should target. Statistical analyses were performed to evaluate the impact of the country of residence and of the patients' age. The survey was answered by 153 caregivers (68%: France, 28%: Germany, and 24%: Italy) off individuals with DS. Individuals with DS included 86 males (mean age of 11.4 [interquartile: 7‐20.4] years). Families ranked as important almost all the items proposed. However, items related to daily life had the highest rank in all three countries compared to items about seizures (P = 0.02). Increase in individuals' age was associated with a higher age at diagnosis (ρ = 0.26, P = 0.02), and a lower impact of seizure duration (ρ = −0.25, P = 0.005) and on the need of hospital referral (ρ = −0.26, P = 0.005). These data can help tailor patient‐centered outcome measures in future clinical and real‐life trials for DS. [ABSTRACT FROM AUTHOR]
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- 2024
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6. Effects of lithium on morpho-physiological and ionomic traits in Cannabis sativa L. microshoots under in vitro conditions.
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Zacchini, Massimo, Gullotta, Giorgio, D'Onofrio, Gianluca, Bertolotto, Pierangelo, Massimi, Lorenzo, and Pietrini, Fabrizio
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The growing demand for lithium (Li) as a key component in battery production is raising concerns about the possible increase in its level in the environmental matrices. Sustainable processes for the remediation of metal-contaminated sites have been targeted, and plants could be useful for this scope. In this regard, the selection of plant material with an improved ability to tolerate and accumulate Li is required. In this work, a proof-of-concept in microshoots cultivated in vitro condition was performed to evaluate the potential of hemp (Cannabis sativa L.) to grow and accumulate Li when exposed to relevant concentrations of this metal in the medium. The results demonstrated the toxic effect of Li on plant growth even at the lowest Li level tested (50 mg L
− 1 ). Increased Li concentrations (150 and 300 mg L− 1 ) caused an impairment of the photosynthetic machinery and an alteration of element uptake, particularly for micronutrients such as Cu, Fe, Zn, Ni, and Co. A remarkable accumulation of Li in the microshoots was detected in relation to the metal concentration in the substrate. The overall data were discussed, providing evidence for the potential of hemp plants to tolerate and accumulate Li. The results of this work could be a reference for further insights into the potential of hemp for Li phytoremediation and phytomining, although the in vitro growth conditions allow them to be highlighted as preliminary indications. Key message: The potential of hemp plants to tolerate and accumulate lithium for phytoremediation and phytomining purposes was evaluated in a proof-of-concept under in vitro culture. [ABSTRACT FROM AUTHOR]- Published
- 2023
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7. Novel biallelic variants expand the phenotype of NAA20‐related syndrome.
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D'Onofrio, Gianluca, Cuccurullo, Claudia, Larsen, Silje Kathrine, Severino, Mariasavina, D'Amico, Alessandra, Brønstad, Kirsten, AlOwain, Mohammed, Morrison, Jennifer L., Wheeler, Patricia G., Webb, Bryn D., Alfalah, Abdullah, Iacomino, Michele, Uva, Paolo, Coppola, Antonietta, Merla, Giuseppe, Salpietro, Vincenzo Damiano, Zara, Federico, Striano, Pasquale, Accogli, Andrea, and Arnesen, Thomas
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GENETIC variation ,MISSENSE mutation ,SYNDROMES ,CATALYTIC activity ,PEOPLE with epilepsy ,EXOMES ,ADOLESCENCE ,PHENOTYPES - Abstract
NAA20 is the catalytic subunit of the NatB complex, which is responsible for N‐terminal acetylation of approximately 20% of the human proteome. Recently, pathogenic biallelic variants in NAA20 were associated with a novel neurodevelopmental disorder in five individuals with limited clinical information. We report two sisters harboring compound heterozygous variant (c.100C>T (p.Gln34Ter) and c.11T>C p.(Leu4Pro)) in the NAA20 gene, identified by exome sequencing. In vitro studies showed that the missense variant p.Leu4Pro resulted in a reduction of NAA20 catalytic activity due to weak coupling with the NatB auxiliary subunit. In addition, unpublished data of the previous families were reported, outlining the core phenotype of the NAA20‐related disorder mostly characterized by cognitive impairment, microcephaly, ataxia, brain malformations, dysmorphism and variable occurrence of cardiac defect and epilepsy. Remarkably, our two patients featured epilepsy onset in adolescence suggesting this may be a part of syndrome evolution. Functional studies are needed to better understand the complexity of NAA20 variants pathogenesis as well as of other genes linked to N‐terminal acetylation. [ABSTRACT FROM AUTHOR]
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- 2023
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8. A real‐life pilot study of the clinical application of pharmacogenomics testing on saliva in epilepsy.
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Riva, Antonella, Roberti, Roberta, D'Onofrio, Gianluca, Vari, Maria Stella, Amadori, Elisabetta, De Giorgis, Valentina, Cerminara, Caterina, Specchio, Nicola, Pietrafusa, Nicola, Tombini, Mario, Assenza, Giovanni, Cappanera, Silvia, Marini, Carla, Rasmini, Paolo, Veggiotti, Pierangelo, Zara, Federico, Russo, Emilio, and Striano, Pasquale
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Response to antiseizure medications (ASMs) can be influenced by several gene polymorphisms, causing either lower efficacy or higher occurrence of adverse drug reactions (ADRs). We investigated the clinical utility of salivary pharmacogenomic testing on epilepsy patients. A commercialized pharmacogenomic salivary test was performed in a cohort of epileptic patients. Genetic variants on five genes (i.e., CYP1A2, CYP2C9, CYP2C19, EPHX1, and ABCB1) involved in common ASMs metabolism were selected. Twenty‐one individuals (median age [Q1–Q3]: 15 [6.5–28] years) were enrolled. Six patients harboring the homozygous *1F allele in CYP1A2 could have reduced chance of response to stiripentol due to fast metabolism. CYP2C9 had reduced activity in 10 patients (alleles *2 and *3), potentially affecting phenytoin (PHT), phenobarbital (PB), primidone, lacosamide (LCM), and valproic acid metabolism. Seven patients, carrying the *2 allele of CYP2C19, had an increased risk of ADRs with clobazam (CLB), PB, PHT, LCM, brivaracetam; while one individual with the *17 allele in heterozygosity reported a CLB fast metabolism. Six patients showed a CC polymorphism of EPHX1 associated with the impaired efficacy of carbamazepine. ABCB1 polymorphisms related to drug‐resistance (3435 CC) or drug‐sensitive phenotype (CT or TT) were found in 6 out of 7 patients. Pharmacogenomic testing on saliva proved easy and safe in clinical practice to convey information for the management of epileptic patients, especially those resistant to treatment or sensitive to severe ADRs. [ABSTRACT FROM AUTHOR]
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- 2023
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9. Genotype–phenotype correlation in contactin-associated protein-like 2 (CNTNAP-2) developmental disorder.
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D'Onofrio, Gianluca, Accogli, Andrea, Severino, Mariasavina, Caliskan, Haluk, Kokotović, Tomislav, Blazekovic, Antonela, Jercic, Kristina Gotovac, Markovic, Silvana, Zigman, Tamara, Goran, Krnjak, Barišić, Nina, Duranovic, Vlasta, Ban, Ana, Borovecki, Fran, Ramadža, Danijela Petković, Barić, Ivo, Fazeli, Walid, Herkenrath, Peter, Marini, Carla, and Vittorini, Roberta
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CELL adhesion ,LITERATURE reviews ,AUTISM spectrum disorders ,GENETIC variation ,MEMBRANE proteins ,DEVELOPMENTAL delay - Abstract
Contactin-associated protein-like 2 (CNTNAP2) gene encodes for CASPR2, a presynaptic type 1 transmembrane protein, involved in cell–cell adhesion and synaptic interactions. Biallelic CNTNAP2 loss has been associated with "Pitt-Hopkins-like syndrome-1" (MIM#610042), while the pathogenic role of heterozygous variants remains controversial. We report 22 novel patients harboring mono- (n = 2) and bi-allelic (n = 20) CNTNAP2 variants and carried out a literature review to characterize the genotype–phenotype correlation. Patients (M:F 14:8) were aged between 3 and 19 years and affected by global developmental delay (GDD) (n = 21), moderate to profound intellectual disability (n = 17) and epilepsy (n = 21). Seizures mainly started in the first two years of life (median 22.5 months). Antiseizure medications were successful in controlling the seizures in about two-thirds of the patients. Autism spectrum disorder (ASD) and/or other neuropsychiatric comorbidities were present in nine patients (40.9%). Nonspecific midline brain anomalies were noted in most patients while focal signal abnormalities in the temporal lobes were noted in three subjects. Genotype–phenotype correlation was performed by also including 50 previously published patients (15 mono- and 35 bi-allelic variants). Overall, GDD (p < 0.0001), epilepsy (p < 0.0001), hyporeflexia (p = 0.012), ASD (p = 0.009), language impairment (p = 0.020) and severe cognitive impairment (p = 0.031) were significantly associated with the presence of biallelic versus monoallelic variants. We have defined the main features associated with biallelic CNTNAP2 variants, as severe cognitive impairment, epilepsy and behavioral abnormalities. We propose CASPR2-deficiency neurodevelopmental disorder as an exclusively recessive disease while the contribution of heterozygous variants is less likely to follow an autosomal dominant inheritance pattern. [ABSTRACT FROM AUTHOR]
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- 2023
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10. Clinical and Neurophysiologic Phenotypes in Neonates With BRAT1 Encephalopathy.
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Carapancea, Evelina, Cornet, Marie-Coralie, Milh, Mathieu, De Cosmo, Lucrezia, Huang, Eric J., Granata, Tiziana, Striano, Pasquale, Ceulemans, Berten, Stein, Anja, Morris-Rosendahl, Deborah, Conti, Greta, Mitra, Nipa, Raymond, F. Lucy, Rowitch, David H., Solazzi, Roberta, Vercellino, Fabiana, De Liso, Paola, D'Onofrio, Gianluca, Boniver, Clementina, and Danhaive, Olivier
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- 2023
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11. Urinary metabotypes of newborns with perinatal asphyxia undergoing therapeutic hypothermia.
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Valerio, Enrico, Mardegan, Veronica, Stocchero, Matteo, Cavicchiolo, Maria Elena, Pirillo, Paola, Poloniato, Gabriele, D'Onofrio, Gianluca, Bonadies, Luca, Giordano, Giuseppe, and Baraldi, Eugenio
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ASPHYXIA neonatorum ,THERAPEUTIC hypothermia ,BETAINE ,NEWBORN infants ,CEREBRAL anoxia-ischemia ,MAGNETIC resonance imaging ,ENERGY metabolism - Abstract
Perinatal asphyxia (PA) still occurs in about three to five per 1,000 deliveries in developed countries; 20% of these infants show hypoxic-ischemic encephalopathy (HIE) on brain magnetic resonance imaging (MRI). The aim of our study was to apply metabolomic analysis to newborns undergoing therapeutic hypothermia (TH) after PA to identify a distinct metabotype associated with the development of HIE on brain MRI. We enrolled 53 infants born at >35 weeks of gestation with PA: 21 of them showed HIE on brain MRI (the "HIE" group), and 32 did not (the "no HIE" group). Urine samples were collected at 24, 48 and 72 hours of TH. Metabolomic data were acquired using high-resolution mass spectrometry and analyzed with univariate and multivariate methods. Considering the first urines collected during TH, untargeted analysis found 111 relevant predictors capable of discriminating between the two groups. Of 35 metabolites showing independent discriminatory power, four have been well characterized: L-alanine, Creatine, L-3-methylhistidine, and L-lysine. The first three relate to cellular energy metabolism; their involvement suggests a multimodal derangement of cellular energy metabolism during PA/HIE. In addition, seven other metabolites with a lower annotation level (proline betaine, L-prolyl-L-phenylalanine, 2-methyl-dodecanedioic acid, S-(2-methylpropionyl)-dihydrolipoamide-E, 2,6 dimethylheptanoyl carnitine, Octanoylglucuronide, 19-hydroxyandrost-4-ene-3,17-dione) showed biological consistency with the clinical picture of PA. Moreover, 4 annotated metabolites (L-lysine, L-3-methylhistidine, 2-methyl-dodecanedioic acid, S-(2-methylpropionyl)-dihydrolipoamide-E) retained a significant difference between the "HIE" and "no HIE" groups during all the TH treatment. Our analysis identified a distinct urinary metabotype associated with pathological findings on MRI, and discovered 2 putative markers (L-lysine, L-3-methylhistidine) which may be useful for identifying neonates at risk of developing HIE after PA. [ABSTRACT FROM AUTHOR]
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- 2022
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12. Genotype-phenotype correlations and disease mechanisms in PEX13-related Zellweger spectrum disorders.
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Borgia, Paola, Baldassari, Simona, Pedemonte, Nicoletta, Alkhunaizi, Ebba, D'Onofrio, Gianluca, Tortora, Domenico, Calì, Elisa, Scudieri, Paolo, Balagura, Ganna, Musante, Ilaria, Diana, Maria Cristina, Pedemonte, Marina, Vari, Maria Stella, Iacomino, Michele, Riva, Antonella, Chimenz, Roberto, Mangano, Giuseppe D., Mohammadi, Mohammad Hasan, Toosi, Mehran Beiraghi, and Ashrafzadeh, Farah
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Background: Pathogenic variants in PEX-genes can affect peroxisome assembly and function and cause Zellweger spectrum disorders (ZSDs), characterized by variable phenotypes in terms of disease severity, age of onset and clinical presentations. So far, defects in at least 15 PEX-genes have been implicated in Mendelian diseases, but in some of the ultra-rare ZSD subtypes genotype-phenotype correlations and disease mechanisms remain elusive.Methods: We report five families carrying biallelic variants in PEX13. The identified variants were initially evaluated by using a combination of computational approaches. Immunofluorescence and complementation studies on patient-derived fibroblasts were performed in two patients to investigate the cellular impact of the identified mutations.Results: Three out of five families carried a recurrent p.Arg294Trp non-synonymous variant. Individuals affected with PEX13-related ZSD presented heterogeneous clinical features, including hypotonia, developmental regression, hearing/vision impairment, progressive spasticity and brain leukodystrophy. Computational predictions highlighted the involvement of the Arg294 residue in PEX13 homodimerization, and the analysis of blind docking predicted that the p.Arg294Trp variant alters the formation of dimers, impairing the stability of the PEX13/PEX14 translocation module. Studies on muscle tissues and patient-derived fibroblasts revealed biochemical alterations of mitochondrial function and identified mislocalized mitochondria and a reduced number of peroxisomes with abnormal PEX13 concentration.Conclusions: This study expands the phenotypic and mutational spectrum of PEX13-related ZSDs and also highlight a variety of disease mechanisms contributing to PEX13-related clinical phenotypes, including the emerging contribution of secondary mitochondrial dysfunction to the pathophysiology of ZSDs. [ABSTRACT FROM AUTHOR]- Published
- 2022
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13. Pharmacodynamic rationale for the choice of antiseizure medications in the paediatric population.
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D'Onofrio, Gianluca, Roberti, Roberta, Riva, Antonella, Russo, Emilio, Verrotti, Alberto, Striano, Pasquale, and Belcastro, Vincenzo
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- 2024
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14. Sleep Exacerbations and Facial Twitching: Diagnostic Clues for ADCY5 -Related Dyskinesias.
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Nosadini, Margherita, D'Onofrio, Gianluca, Pelizza, Maria Federica, Luisi, Concetta, Padrin, Davide, Baggio, Laura, Zorzi, Giovanna Simonetta, Toldo, Irene, and Sartori, Stefano
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ADENYLATE cyclase ,MOVEMENT disorders ,CHOREA ,DYSKINESIAS ,DYSTONIA - Abstract
Background Mutations in the adenylate cyclase 5 (ADCY5) gene are associated with childhood-onset paroxysmal dyskinesia. Methods We report a new video-documented case of pediatric ADCY5 -related dyskinesia with de novo ADCY5 mutation. Results A boy born to nonconsanguineous parents after an uneventful pregnancy had developmental delay and hypotonia. At the age of 7 months, he presented with paroxysmal jerky–choreic–dystonic involuntary movements in wakefulness involving limbs, trunk, and face, exacerbated by emotional stimuli. These episodes gradually worsened in duration and frequency: at the age of 2.5 years, they occurred up to six times per day, and appeared also during sleep in prolonged bouts; the boy also had basal choreoathetoid–dystonic movements, hyperactivity, paraparetic–ataxic gait, generalized hypotonia with brisk tendon reflexes, drooling, and language delay with intellectual disability. Brain magnetic resonance imaging, electroencephalogram, electromyogram, eye review, metabolic investigations, oligoclonal bands, and autoantibodies were normal. Extensive genetic testing had not let to a diagnosis, until a heterozygous de novo mutation c.1252C > T (p.Arg418Trp) was identified in the ADCY5 gene. Clonazepam had partial effectiveness. The boy walked at the age of 3.5 years. At the age of 5 years, the paroxysmal movement disorder has slightly improved. Conclusion ADCY5 mutations should be considered among the differential diagnoses of early-onset paroxysmal choreic–athetosic–myoclonic–dystonic movement disorder involving limbs, trunk, and face, in patients with global neurological impairment with hypotonia and developmental delay. Facial dyskinesias and exacerbation by drowsiness/sleep and emotional stimuli are important clues that may allow a timely recognition of the disorder and avoidance of unnecessary diagnostic investigations. [ABSTRACT FROM AUTHOR]
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- 2021
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15. Add‐on cannabidiol significantly decreases seizures in 3 patients with SYNGAP1 developmental and epileptic encephalopathy.
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Kuchenbuch, Mathieu, D'Onofrio, Gianluca, Chemaly, Nicole, Barcia, Giulia, Teng, Théo, and Nabbout, Rima
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SEIZURES (Medicine) ,CANNABIDIOL ,SYNCOPE ,AUTISM spectrum disorders ,DEVELOPMENTAL delay ,VAGUS nerve ,MULTIDRUG-resistant tuberculosis ,AUTOMATED external defibrillation - Abstract
Mutations in SYNGAP1 are associated with developmental delay, epilepsy, and autism spectrum disorder (ASD). Epilepsy is often drug‐resistant in this syndrome with frequent drop attacks. In a prospective study of add‐on cannabidiol (CBD), we identified three patients with SYNGAP1 mutations: two boys and one girl. Seizure onset was at 3.5, 8, and 18 months (M), respectively, with numerous atypical absences per day associated with eyelid myoclonia (2/3 patients), upper limb myoclonic jerks (2/3 patients), and drop attacks (all patients). Seizures were resistant to at least 5 antiepileptic drugs (AEDs). After CBD introduction, two patients were responders since M2 and achieve a seizure reduction of 90% and 80%, respectively, at M9 with disappearance of drop attacks. EEGs showed an improvement regarding background activity and interictal anomalies. The last patient showed a late response at M7 of treatment with an 80% decrease in seizure frequency. Caregiver in all three evaluated as much improved the status of their children. Treatment was well‐tolerated in all, and no major adverse events (AEs) were reported. CBD showed efficacy in patients with drug‐resistant epilepsy due to SYNGAP1 mutations. Other patients with rare genetic developmental and epileptic encephalopathies with drug‐resistant epilepsies might benefit from CBD. [ABSTRACT FROM AUTHOR]
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- 2020
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16. Slow Titration of Cannabidiol Add-On in Drug-Resistant Epilepsies Can Improve Safety With Maintained Efficacy in an Open-Label Study.
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D'Onofrio, Gianluca, Kuchenbuch, Mathieu, Hachon-Le Camus, Caroline, Desnous, Béatrice, Staath, Véronique, Napuri, Sylvia, Ville, Dorothée, Pedespan, Jean-Michel, Lépine, Anne, Cances, Claude, de Saint-Martin, Anne, Teng, Théo, Chemaly, Nicole, Milh, Mathieu, Villeneuve, Nathalie, and Nabbout, Rima
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CANNABIDIOL ,VOLUMETRIC analysis ,TUBEROUS sclerosis ,BEHAVIOR disorders ,EPILEPSY ,LENNOX-Gastaut syndrome - Abstract
Objective: To assess adverse events (AEs) and efficacy of add-on cannabidiol (CBD) with a slower titration protocol in pediatric clinical practice. Methods: We conducted a prospective, open-label, multicenter study in seven French reference centers for rare epilepsies. Patients had slow titration to reach a target dose of 10 mg/kg/day within at least 1 month and then gradually increased to a maximum dose of 20 mg/kg/day. We analyzed AEs and efficacy at M1 (month 1), M2, and M6, comparing two sets of subgroups: Dravet syndrome (DS) vs. Lennox-Gastaut (LGS) and patients with clobazam (CLB+) vs. patients without (CLB−). Results: One hundred and twenty-five patients were enrolled (62 LGS, 48 DS, 5 Tuberous sclerosis, and 10 other etiologies). Median concomitant antiepileptic drugs (AEDs) was three (25th percentile: 3, 75th percentile: 4). Patients received a dose of 10 (10–12), 14 (10–20), and 15.5 mg/kg/day (10–20) at M1, M2, and M6, respectively. Twenty-six patients discontinued CBD, 19 due to lack of efficacy, 2 due to AEs, 4 for both, and 1 had a sudden unexpected death in epilepsy. AEs were reported in 61 patients (48.8%), mainly somnolence (n = 26), asthenia (n = 20), and behavior disorders (n = 16). Abnormal transaminases (≥3 times) were reported in 11 patients receiving both valproate and clobazam. AEs were significantly higher at M2 (p = 0.03) and increased with the number of AEDs (p = 0.03). At M6, total seizure frequency change from baseline was −41% ± 37.5% (mean ± standard deviation), and 28 patients (37.8%) had a reduction ≥50%. AE and efficacy did not differ between DS vs. LGS and CLB+ vs. CLB– patients. Significance: A slower titration of CBD dose delivered better tolerance with comparable efficacy to previous trials. Concomitant CLB did not increase efficacy rates but in a few cases increased AEs. This slow titration scheme should help guide clinicians prescribing CBD and allow patients to benefit from its potential efficacy. [ABSTRACT FROM AUTHOR]
- Published
- 2020
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