CBD-enriched cannabis for autism spectrum disorder: an experience of a single center in Turkey and reviews of the literature
Introduction: Autism spectrum disorder is a neurodevelopmental disorder characterized by deficits in communication, social interaction, restricted interest, and repetitive behaviors. Although more cases are being diagnosed, no drugs are approved to treat the core symptoms or cognitive and behavioral problems associated with autism. Therefore, there is an urgent need to develop an effective and safe treatment.
Objective: In this study, we aim to share our 2-year experience with CBD-enriched cannabis treatment in autism and review the latest studies.
Materials and methods: The study included 33 (27 males, six females) children diagnosed with autism spectrum disorder who were followed up between January 2018 and August 2020. The mean age was 7.7 ± 5.5 years. The average daily dosage of cannabidiol (CBD) was 0.7 mg/kg/day (0.3-2 mg/kg/day). The median duration of treatment was 6.5 months (3-28 months). The preparations used in this study contained full-spectrum CBD and trace elements tetrahydrocannabinol (THC) of less than 3%.
Results: The outcomes were evaluated before and after treatment based on clinical interviews. At each follow-up visit, parents were asked to evaluate the effectiveness of the CBD-enriched cannabis treatment. According to the parents’ reports, no change in daily life activity was reported in 6 (19.35%) patients. The main improvements of the treatment were as follows: a decrease in behavioral problems was reported in 10 patients (32.2%), an increase in expressive language was reported in 7 patients (22.5%), improved cognition was reported in 4 patients (12,9%), an increase in social interaction was reported in 3 patients (9.6%), and a decrease in stereotypes was reported in 1 patient (3.2%). The parents reported improvement in cognition among patients who adhered to CBD-enriched cannabis treatment for over two years. The antipsychotic drug could be stopped only in one patient who showed mild ASD symptoms. No change could be made in other drug use and doses. Additionally, this study includes an extensive review of the literature regarding CBD treatment in autism spectrum disorder. According to recent studies, the average dose of CBD was 3.8±2.6 mg/kg/day. The ratio of CBD to THC in the used preparations was 20:1. The most significant improvements were seen in the behavioral problems reported in 20-70% of the patients.
Conclusion: Using lower doses of CBD and trace THC seems to be promising in managing behavioral problems associated with autism. In addition, this treatment could be effective in managing the core symptoms and cognitive functions. No significant side effects were seen at the low doses of CBD-enriched cannabis when compared to other studies.
Keywords: Autism spectrum disorder; Cannabidiol; Cannabis.
CBD-enriched cannabis for autism spectrum disorder: an experience of a single center in Turkey and reviews of the literature
Autism spectrum disorder is a neurodevelopmental disorder characterized by deficits in communication, social interaction, restricted interest, and repetitive behaviors. Although more cases are being diagnosed, no drugs are approved to treat the core symptoms or cognitive and behavioral problems associated with autism. Therefore, there is an urgent need to develop an effective and safe treatment.
In this study, we aim to share our 2-year experience with CBD-enriched cannabis treatment in autism and review the latest studies.
Materials and methods
The study included 33 (27 males, six females) children diagnosed with autism spectrum disorder who were followed up between January 2018 and August 2020. The mean age was 7.7 ± 5.5 years. The average daily dosage of cannabidiol (CBD) was 0.7 mg/kg/day (0.3–2 mg/kg/day). The median duration of treatment was 6.5 months (3–28 months). The preparations used in this study contained full-spectrum CBD and trace elements tetrahydrocannabinol (THC) of less than 3%.
The outcomes were evaluated before and after treatment based on clinical interviews. At each follow-up visit, parents were asked to evaluate the effectiveness of the CBD-enriched cannabis treatment. According to the parents’ reports, no change in daily life activity was reported in 6 (19.35%) patients. The main improvements of the treatment were as follows: a decrease in behavioral problems was reported in 10 patients (32.2%), an increase in expressive language was reported in 7 patients (22.5%), improved cognition was reported in 4 patients (12,9%), an increase in social interaction was reported in 3 patients (9.6%), and a decrease in stereotypes was reported in 1 patient (3.2%). The parents reported improvement in cognition among patients who adhered to CBD-enriched cannabis treatment for over two years. The antipsychotic drug could be stopped only in one patient who showed mild ASD symptoms. No change could be made in other drug use and doses. Additionally, this study includes an extensive review of the literature regarding CBD treatment in autism spectrum disorder. According to recent studies, the average dose of CBD was 3.8±2.6 mg/kg/day. The ratio of CBD to THC in the used preparations was 20:1. The most significant improvements were seen in the behavioral problems reported in 20–70% of the patients.
Using lower doses of CBD and trace THC seems to be promising in managing behavioral problems associated with autism. In addition, this treatment could be effective in managing the core symptoms and cognitive functions. No significant side effects were seen at the low doses of CBD-enriched cannabis when compared to other studies.
Autism spectrum disorder (ASD) is a neurodevelopmental disorder that varies in severity and is characterized by deficits in communication, social interaction, restricted interest, and repetitive behaviors (Fusar-Poli et al. 2020). During the last three decades, there has been a threefold increase in the number of children diagnosed with ASD (Lihi Bar-Lev Schleider et al. 2019). Currently, it affects up to 1 in 54 individuals (Maenner et al. 2020). Cooccurring medical conditions such as epilepsy, intellectual disability, and behavior problems occur in these individuals (Pretzsch et al. 2019a; Pretzsch et al. 2019b).
The etiopathogenesis of ASD remains largely unknown. Several genetic, perinatal, and environmental factors seem to be involved. Some researchers have evidenced an imbalance in the endogenous neurotransmission system, such as the serotoninergic, γ aminobutyric acid (GABA), and endocannabinoid system (ECS), which regulate functions such as emotional responses and social interactions typically impaired in ASD (Fusar-Poli et al. 2020).
Endocannabinoids (eCBs) and their receptors are present in the nervous system, connective tissue of internal organs, glands, and immune system. Cannabinoid receptor 1 (CB1) is a G protein-coupled receptor (GPR) that is found mainly in the central nervous system (Mc Partlan et al. 2014). In mammals, high concentrations of CB1 are found in the brain area that regulates appetite, memory, fear extinction, motor responses, and postures such as the hippocampus, basal ganglia, basolateral amygdala, hypothalamus, and cerebellum (Aran et al. 2019; Mc Partlan et al. 2014). CB1 can also be found in nonneuronal cells. Data indicate that cannabinoid receptor type 2 (CB2) is linked to a variety of immune functional events. However, it may play a functionally relevant role in the central nervous system (Aran et al. 2019; Bridgemanan and Abazia 2017).
There are two endogenous cannabinoids, N-arachidonoylethanolamine (anandamide) and two arachidonoylglycerols (2-AG). The ECS has been broadened by discovering new secondary receptors, ligands, and ligand metabolic enzymes, including transient receptor potential cation channel subfamily V member 1 (TRPV1) (Mc Partlan et al. 2014).
Anandamide and 2-AG can act via CB1 and CB2 receptors and exert a range of biological effects in central and peripheral cells. Anandamide is broken down by fatty acid amide hydrolase (FAAH); inhibitors of FAAH lead to an increase in anandamide. CBD act as an inhibitor of FAAH (Bridgemanan and Abazia 2017). Endocannabinoid signaling occurs in a retrograde direction; that is, signaling is initiated in postsynaptic neurons and acts upon presynaptic terminals. In contrast to classical neurotransmitters, eCBs are not stored. They are produced on demand upon stimulation of postsynaptic cells (Aran et al. 2019; Zamberletti et al. 2017).
Interestingly, CBD displays a low affinity for CB1 and CB2 receptors. CBD facilitates excitatory glutamate and inhibitory GABA neurotransmission across the brain through agonism at the TRPV1 receptor (Pretzsch et al. 2019a; Mc Partlan et al. 2014). Additionally, CBD can increase GABAergic transmission by antagonizing G protein-coupled receptor 55 (GPR55), especially in the basal ganglia. CBD is thought to be an agonist at prefrontal serotonin 5-HT1A receptors (Castillo et al. 2012) (Fig. 1).
CBD and mechanism of action. CBD, cannabidiol; FAAH, fatty acid amide hydrolase CB, cannabinoid receptor; TRPV1, transient receptor potential cation channel subfamily V member 1; PPAR-γ, peroxisome proliferator-activated receptor-gamma; GPR, G protein-coupled receptor; GPR55, G protein-coupled receptor 55; 5-HT1A, serotonin 5HT receptor; MC4R, melanocortin 4 receptor; ROS, reactive oxygen species
Another mechanism of action can be via vasopressin and oxytocin. The presence of oxytocin in the CSF seems to originate from neuronal oxytocinergic extensions to the limbic system, brain stem, and spinal cord. Oxytocin receptors are distributed in different parts of the central nervous system, such as the basal ganglia, limbic system, thalamus and hypothalamus, and brain stem. Oxytocin modulates social behavior, motor function, pain control, memory and learning, eating behavior, stress and anxiety, and emotional processing. Oxytocin administration reduces stress and anxiety and depression in animal models. This effect seems to be modulated at least partly by the effects of oxytocin on the hypothalamic-pituitary-adrenal (HPA) axis and the opioidergic and dopaminergic systems in limbic brain structures. Several animal model studies support the role of oxytocin in improving social behavior, an effect that appears to involve the melatoninergic and endocannabinoid systems, specifically an increase in social interactions produced by agonism at the melanocortin four receptor (MC4R (Russo et al. 2005; Dos Santos et al. 2019). CBD leads to enhancement in the release of vasopressin and oxytocin; thus, it could positively affect ASD core symptoms. Studies have shown that oxytocin administration to patients with ASD improves social interactions, reduces classic repetitive behavior, and increases eye contact (Weia et al. 2015). Another mechanism of action of CBD is to act as a dopamine receptor antagonist, which can facilitate its use as an antipsychotic (Dos Santos et al. 2019; Weia et al. 2015).
CBD may act as a neuroprotectant against mitochondrially acting toxins (Davies and Bhattacharyya 2019; Bartova and Birmingham 1976). The highly lipophilic aspect of CBD gives them access to intracellular sites of action. Many studies have suggested mitochondria as targets for CBD, and many theories are based on this idea; one of these theories is that the outer mitochondrial membrane has CB1 receptors. This theory reveals that CBD affects the function of the cells by establishing homeostasis and influencing mitochondria and energy production (Bartova and Birmingham 1976; Ryan et al. 2009).
THC is known to be a major psychoactive component of Cannabis. THC is a partial agonist at CB1 and CB2 (Ryan et al. 2009). Signals through transducing G-proteins and activation of these G-proteins by THC cause inhibition of adenyl cyclase activity, the closing of voltage-gated calcium channels, and the opening of inward rectifying potassium channels. The psychoactive nature of THC limits its use due to side effects. However, a varied mixture of THC with other phytocannabinoids with very weak or no psychoactivity quality has started to be used as a therapeutic drug in humans (Bloomfield et al. 1982; Rodríguez De Fonseca et al. 1992). In this study, we aim to share our 2-year experiences with CBD-enriched cannabis treatment in autism and review the latest studies.
Methods and materials
This research was conducted in accordance with the Declaration of Helsinki at the Pediatric Clinics of Neurology in Istanbul. CBD-enriched cannabis treatment was started in 54 patients who were diagnosed with ASD. The study included 33 (27 males, six females) children diagnosed with autism spectrum disorder who were followed up between January 2018 and August 2020. The diagnosis of ASD was based on DSM V criteria (American Psychiatric Association 2013). Twenty-one participants refused to participate in this study. The most common reasons for not participating in the study were fear of adverse effects, cost of CBD-enriched cannabis, bitter taste, and behavioral problems. The mean age of the non-participating 21 children was 7.2 ± 4.2. Ten patients had mild, while 11 had severe autism according to the DSM V. Four patients were female, and 17 were male. Three children had abnormal EEG, and one was diagnosed with epilepsy, and he was on valproic acid treatment. Three patients attended mainstream schools and received their education there, while eighteen patients had intellectual disabilities. All non-participating 21 ASD patients used antipsychotic drugs. Sixteen patients used risperidone, and five patients used aripiprazole. The median duration of antipsychotic drug administration was 8.2 ± 2.6 months. The median duration of follow-up was 4.4 1 ± 1 years.
Informed consent was obtained from the parents of all children participating in the study. The mean age of the participating 33 children was 7.7 ± 5.5. Fifteen patients had mild autism, while 18 had severe autism according to the DSM V. Three patients were diagnosed with epilepsy before starting CBD-enriched cannabis; two of them used oxcarbazepine, while one used valproic acid. Seven patients had abnormal electroencephalography (EEG) results without any episodes of previous seizures. Five patients attended mainstream schools and received their education there, while twenty-eight patients had intellectual disabilities and attended schools that catered to special educational needs. Two patients were using CBD-enriched cannabis for over two years. There was no predefined duration of this treatment in our patients. All ASD patients used antipsychotic drugs. Twenty-six patients used risperidone, and seven patients used aripiprazole. The median duration of antipsychotic drug administration was 8.5 ± 2.3 months. All the patients were provided with psychosocial treatment. The median duration of follow-up was 4.6 ± 1.3 years. There were no significant differences between the 2 group profiles (participating and non-participating) regarding sex ratio, median age, and autism severity.
The legal basis for using cannabis-related drugs is not fully apparent in Turkey, and a maximum of 0.3% THC is allowed to be used in these preparations. Due to the lack of availability and difficulty of access to these therapeutic preparations, various cannabis strains of CBD-enriched cannabis extracts have been used. The two CBD-enriched cannabis brands used were CBDistillery and CBDodgamax. Both had similar available forms of drops of 500, 1000, and 2500 mg/30 ml and contained full-spectrum CBD and trace THC. These drops were started with dosages that were calculated according to the patient’s body weight, with one sublingual drop twice a day and one drop every three days. The average daily CBD-enriched cannabis dose was 0.7 mg/kg (0.3–2 mg/kg). No patient was given a daily maintenance dose of CBD higher than 40 mg/day. The average duration of treatment was 6.5 months (3–28 months).
Results and outcomes
The outcomes were evaluated before and after treatment based on clinical interviews. At each follow-up visit, parents were asked to assess the overall effectiveness of CBD-enriched cannabis treatment. According to the parents’ reports, no change in daily life activity was reported in 6 (19.35%) patients. The main improvements of the treatment were as follows: a decrease in behavioral problems was reported in 10 patients (32.2%), an increase in expressive language was reported in 7 patients (22.5%), improved cognition was reported in 4 patients (12.9%), an increase in social interaction was reported in 3 patients (9.6%), and a decrease in stereotypes was reported in 1 patient (3.2%). The parents reported improvement in cognition in patients who adhered to CBD-enriched cannabis treatment for over two years. The antipsychotic drug could be stopped only in one patient who showed mild ASD symptoms. No change could be made in other drug use and doses.
Discontinuation and side effects
A 13-year-old male patient with severe autism had generalized seizures after using 5 mg sublingual CBD, and the drug was discontinued because of this side effect. The epileptic seizures persisted despite the discontinuation of the treatment. Interictal sleep EEG showed symmetrical bilateral frontotemporal sharp-slow wave complexes. The patient was regularly treated with valproic acid and remained seizure-free after starting this antiepileptic drug. CBD-enriched cannabis was also discontinued in a nine-year-old male patient with severe autism after two weeks because of a significant increase in stereotypes. No change in laboratory values related to CBD-enriched cannabis was found in any patient.
Restlessness was the only reported side effect in 7 (22%) out of 31 patients who continued treatment for at least three months, and the CBD-enriched cannabis dose was reduced in these patients. As the amount was reduced, restlessness decreased.
A review of other studies
The popularity of CBD-enriched cannabis for the treatment of autism is increasing. Scoping reviews were done to achieve a broad and thorough examination of the literature in this area. Aran et al. (2019) were the first to retrospectively assess CBD-enriched cannabis effects on 60 children with ASD and severe behavioral problems using an open-label cohort study. The mean age was 11.8 ± 3.5 years; 82% of patients used psychiatric medications; 77% of patients had low cognitive function; and 23.3% of patients had epilepsy. All the children received CBD and THC in a 20:1 ratio. The mean total daily dose was 3.8 ± 2.6 mg/kg/day CBD and 0.29 ± 0.22 mg/kg/day THC for children who received three daily doses (n=44) and 1.8 ± 1.6 mg/kg/day CBD and 0.22 ± 0.14 mg/kg/day THC for children who received two daily doses (n=16). The doses were titrated over 2–4 weeks. The mean follow-up period was 10.9 ± 2.3 months. Efficacy was assessed using the Caregiver Global Impression of Change (CaGI) scale. Considerable improvement in behavioral problems was noticed in 61% of patients. Improvement in anxiety and communication problems was seen in 39 and 47%, respectively. Based on these promising results, Aren et al. launched a new placebo-controlled crossover trial. This study is ongoing, and new outcomes will be addressed in future publications (Aran et al. 2019).
Another study was conducted to evaluate the efficacy and safety of CBD-enriched cannabis effects on autism. This prospective, open-label study was carried out by Lihi Bar-Lev Schleider et al. and included 188 patients. The mean age was 12.9 ± 7 years. A total of 14.4% of patients had epilepsy. Most patients used preparations with 30% CBD and 1.5% THC, and the average concentrations of CBD and THC were 79.5 ± 61.5 mg and 4.0 ± 3.0 mg, respectively. After one month of treatment, 179 patients adhered to the treatment, and only 119 patients could be evaluated. Significant improvement was reported in 48.7% of patients, moderate improvement was reported in 31.1% of patients, and no change was reported in 14.3% of patients. Side effects were reported in 5.9% of patients. After 6 months of treatment, 155 patients continued treatment with CBD. Of the latter group, 93 patients responded to the questionnaire, 30.1% reported significant improvement, 53.7% reported moderate improvement, 6.4% reported slight amelioration, and 8.6% of the patients reported no change. Quality of life, mood, and ability to perform daily living activities were evaluated before the treatment and at 6 months. A total of 31.3% of the patients reported good quality of life before treatment. After 6 months, this percentage increased up to 66.8% (Lihi Bar-Lev Schleider et al. 2019).
Paulo Fleury et al. (2019) conducted a prospective, observational, and open-label study with a cohort of 18 autistic patients who received CBD-enriched cannabis (with a CBD-to-THC ratio of 75/1). The average dose of CBD was 4.55 mg/kg/day (a minimum of 3.75 mg and a maximum of 6.45 mg/kg/day). The average THC dose was 0.06 mg/kg/day (a minimum of 0.05 and a maximum of 0.09 mg/kg/day). The mean age was ten years. Fifteen patients adhered to the treatment (10 nonepileptic and five epileptic), and only one patient showed a lack of improvement in autistic behaviors. The most significant improvements were reported for seizures, attention-deficit/hyperactivity disorder, sleep disorders, communication, and social interaction (Paulo Fleury et al. 2019). Barchel et al. (2019) performed an open-label study on 53 autistic children. The median age was 11 (4–22) years; these patients received CBD at a concentration of 30% and a 1:20 ratio of CBD to THC. The median THC interquartile range (IQR) daily dose was 7 (4–11) mg, and the median CBD (IQR) daily dose was 90 (45–143) mg. The median duration of treatment was 66 days (30–588). Self-injury and rage attacks improved by 67.6% and worsened by 8.8%, respectively. Improvement in hyperactivity symptoms was reported in 68.4% of patients, 28.9% reported no change, and 2.6% reported worsening symptoms. Sleep problems improved by 71.4% and worsened by 4.7%. There was an improvement in anxiety in 47.1% and worsening in 23.5% of patients (Barchel et al. 2019). Mojdeh Mostafavi et al. (2020) reported positive effects of cannabis in ASD, especially in aggressive and self-injurious behaviors (Mostafavi and Gaitanis 2020). McVige et al. (2020) carried out an important retrospective and open-label study on 20 patients with ASD (6 with epilepsy and 14 with pain). These patients were on cannabis treatment. The study reported very significant positive outcomes. The Autism/Caregiver Global Impression of Change (ACGIC) scale revealed improvements in sleep, mood, and aggression toward the self or others; there were also improvements in patient communication abilities and attention/concentration (McVige et al. 2020).
According to Aren et al.’s study, adverse events such as hypervigilance aggravated sleep disturbances in 14% of patients. This side effect was resolved by omitting or adjusting the evening doses. Irritability in 9% and loss of appetite in 9% were seen. A thirteen-year-old girl received 6.5 mg/kg/day CBD and no other medications; when she gradually increased the THC dose up to 0.72 mg/kg/day, she developed sudden behavioral changes such as unusual vocalization and refusal to sleep and eat for two days. The symptoms resolved when she stopped CBD and THC and received antipsychotic treatment (ziprasidone). After cannabis treatment, psychiatric medications were regulated in most patients; 33% received fewer or lower doses, 24% stopped taking medications, and 8% received more medication or higher doses (Aran et al. 2019). Lihi Bar-Lev Schleider et al. reported mild side effects such as restlessness, sleepiness, dry mouth, and digestion problems (Lihi Bar-Lev Schleider et al. 2019). Paulo Fleury et al. reported that three patients stopped using CBD-enriched cannabis in a period shorter than one month due to side effects (autistic behaviors had worsened in two patients, which might happen due to the unsupervised and sudden cessation of the antipsychotics; one patient had insomnia, irritability, increased heart rate, and worsening of psych-behavioral crises that might be due to the interaction of cannabis with previous prescribed antipsychotic drugs). Mild and transient adverse effects such as sleepiness, moderate irritability, diarrhea, increased appetite, conjunctival hyperemia, and increased body temperature were also reported (Paulo Fleury et al. 2019).
In the updated review, preliminary evidence announcing that cannabinoids (compounds with different ratios of CBD and THC) could exert beneficial effects on some ASD-associated symptoms, such as behavioral problems, hyperactivity, and sleep disorders, with a lower number of metabolic and neurological side effects than approved medications. Importantly, treatment with cannabinoids permits a reduction in the number of prescribed drugs and significantly reduces the frequency of seizures in participants with comorbid epilepsy. In this paper, we aimed to make some critical points related to the main findings and mechanisms of action of cannabinoids, such as a decrease in behavioral problems, an increase in the expressive language, an improvement in cognition, and an increase in social interaction when patients used CBD-enriched cannabis at a dose of 0.7 mg/kg (0.3–2 mg/kg), which is lower than the doses reported in other studies. Furthermore, these results are consistent with other studies that suggest that supplementing ASD patients with CBD-enriched cannabis could improve behavioral problems. A dose of 3.8 ± 2.6 mg/kg/day CBD was used in Aren et al.’s study and yielded improvements in anxiety and communication problems. According to Paulo Fleury et al., the average dose of CBD was 4,55 mg/kg/day, and the results showed that only one patient reported no improvement in autistic behaviors. The most significant improvements were reported for seizures, attention-deficit/hyperactivity disorder, sleep disorders, communication, and social interaction. In addition, improvements in expressive language were seen. CBD-enriched cannabis might help children with ASD via several possible mechanisms, including its anxiolytic and antipsychotic properties and its impact on the endocannabinoid system (ECS) and oxytocin (Dos Santos et al. 2019; McVige et al. 2020; Premolia et al. 2019). According to our results, we recommend using lower doses of CBD-enriched cannabis.
CBD use is not devoid of health risks; known risks include liver damage, adverse effects on the male reproductive system, potential drug interactions that may be associated with adverse events or diminished efficacy of approved therapies, and additional unknown health risks. However, the pharmacology of CBD has not been well studied; thus, little is known about both the potential therapeutic benefits and the hazards of short- or long-term use (Leas et al. 2020). According to our study, restlessness was the only mild side effect seen in some patients which was resolved on making some doses adjustments. In addition, generalized seizures after starting CBD-enriched cannabis. And these seizures re-occurred even several months after cessation of CBD treatment, and abnormal EEG results were seen. Therefore, this study cannot make causal inferences on the relation between CBD-enriched cannabis and seizures. Not all patients benefit equally from the use of CBD. The reason why some patients experienced benefits while others experienced side effects could be due to candidate genes that may influence the acute effects of cannabis. Genes posited to have specific influences on cannabis include CNR1, CB2, FAAH, MGL, TRPV1, and GRP55. When some patients have a mutation in these receptors, different results could be seen when cannabis was used (Agrawal and Lynskey 2009). Other studies also reported reversible and some mild side effects, none of which were life-threatening. Most of the side effects were overcome by adjusting the doses. Furthermore, the use of recreational cannabis in adolescents is associated with several risks, including decreased motivation, addiction, mild cognitive decline, and schizophrenia. However, these complications are all attributed to THC. Our study drug was full-spectrum CBD and trace THC. Nevertheless, systematic evaluation of safety data of CBD use in children is still lacking. Future research is recommended that examines the clinical impact of CBD-enriched cannabis. Additionally, rarer side effects were seen in our patients compared to other studies, which could be due to using lower doses of CBD and trace THC (a brief overview of all these studies is given in Tables 1 and 2).
These preclinical data and the current study results render further exploration of this treatment avenue in controlled studies. Until such evidence is available, physicians should be cautious when using medical cannabis to treat children with ASD since initial reports of promising treatment in children with ASD are often found.
Limitations of the study
The absence of the control study group, the use of various strains of CBD-enriched cannabis extracts, different durations of treatment and dosages, and depending on the reports of the parents instead of standard assessment scales are considered to be the main limitations of the study. The clinical assessments were done with knowledge of the patients’ treatment (it was an open-label case series, not a blinded clinical trial.
Using lower doses of CBD and trace THC seems to be promising in the management of behavioral problems associated with autism. In addition, this treatment could be effective in managing core symptoms and cognitive functions. No significant side effects were seen at the low doses of CBD-enriched cannabis when compared to other studies.
Availability of data and materials
The datasets used and analyzed in this review article are available from the corresponding author upon reasonable request.
CBD for Autism Spectrum Disorder
Autism spectrum disorder (ASD), more often simply referred to as autism, includes a broad range of conditions that are characterized primarily by challenges in basic social skills, repetitive behaviors as well as speech and nonverbal communication.
Autism does not consist of one type, but instead has many subs-types and lie on a spectrum that is most influenced by a combination of genetic and environmental factors. Because of this, each person with autism has a distinct set of strengths and challenges. How different autism sufferers learn, think and problem-solve can range from highly skilled to severely challenged with some people requiring a significant amount of support in their daily lives, while others may live entirely independently, or requiring little support.
There are several factors that influence the development of autism. For instance, ASD is often accompanied by sensory sensitivities and medical issues such as gastrointestinal (GI) disorders, seizures or sleep disorders, as well as mental health challenges such as anxiety, depression and attention issues. These concomitant symptoms and diseases can aggravate the symptoms of autism or interfere with treatment.
Signs and symptoms of ASD usually appear around the age of two or three, however some associated developmental delays can present as early as 18 months of age. Research shows that the earlier the intervention and treatment of ASD, the more positive outcomes can be expected later in life for those suffering from it.
Autism Spectrum Disorder Types
The three types of autism spectrum disorders are:
Autistic disorder: The most severe type, this is sometimes referred to as “classic” autism. People with autistic disorder have significant language delays, social and communication challenges, and unusual behaviors and interests.
Asperger syndrome: This is a milder type of autism spectrum disorder. While people with Asperger’s don’t struggle intellectually, they do have difficulty with social interaction.
Pervasive developmental disorder: This type of autism describes individuals who meet some, but not all, of the criteria for the other subtypes.
Symptoms of Autism Spectrum Disorder
While symptoms vary across the autism spectrum, two common indicators of ASD include:
Social communication challenges
- Social withdrawal
- Unusual reactions in social settings
- Inappropriate social interactions
- A lack of empathy
- A lack of understanding social cues
- Not engaging with play with peers
- Problems with two-way conversations
- An abnormal tone of voice
- The avoidance of eye contact or poor eye contact
- Deficits in language comprehension
- A delay in learning to speak
- Flat or monotonous speech patterns
Restricted, repetitive behavior
- Abnormal body posturing or facial expressions
- Intense focus on one topic
- A preoccupation with specific topics
- Repetitive movements
- Self-abusive behaviors that result in injury and/or self-harm
Other autism symptoms and signs can also include:
- Learning disabilities
- Repeating words or phrases out of context
- Using odd words or phrases
- Sleep disturbances
- Gastrointestinal (GI) disorders such as Irritable Bowel Syndrome and Chron’s disease
Autism Spectrum Disorder Medications and Treatments
Although doctors haven’t identified a cure for autism, there are treatment options that can aid people with ASD in their everyday life that can include a combination of medicines and behavioral interventions.
There are no medications that can cure ASD, but can help manage problems with aggression, irritability, behavioral reactivity, self-injury and repetitive behaviors. Certain medications may also help reduce high energy levels and hyperactivity, aid with focus, reduce the symptoms of anxiety and depression or manage seizure activity.
The core interventions for helping people with ASD are aimed at managing the core challenges of behavior and social interactions, for which several treatments have proven to be helpful. The include:
- Behavior and Communication Approaches including Applied Behavioral Analysis (ABA) like Discrete Trial Training (DTT) and Early Intensive Behavioral Intervention (EIBI) which build positive behaviors and reduce unwanted behaviors, Occupational Therapy, Social Skills Training, Speech Therapy and assistive technologies such as communication boards and electronic tablets
- Dietary Approaches are aimed primarily at improving biomedical markers, although some parents feel that dietary changes make a difference in how their child acts or feels. Dietary treatments are based on the idea that food allergies or lack of vitamins and minerals can aggravate symptoms of ASD with changes including the removal of certain foods and using vitamin or mineral supplements.
- Complementary and Alternative Medicine (CAM) can help relieve the symptoms of ASD. CAM treatments for ASD include chelation (a treatment to remove heavy metals such as lead from the body), biologicals (for example, secretin), or mind-body medicine. However, many of these treatments have not been studied for effectiveness.
CBD and Autism Spectrum Disorder
Research and Scientific Evidence
There is an increasing interest in the use of cannabinoids as a treatment for mental health and neurodevelopmental disorders. This has also given rise to an increase in investigations into the effectiveness of Cannabidiol (CBD) for the treatment and management of ASD symptoms, especially those related to behavior, with many researchers concluding that it has the potential to help those suffering from autism.
Cannabidiol Based Medical Cannabis in Children with Autism- a Retrospective Feasibility Study
Researchers published the results of a 2018 retrospective study in Neurology . Their objective was to assess the efficacy, tolerability and safety of CBD as an adjuvant therapy for refractory behavioral difficulties in children suffering from ASD.
They administered oral CBD and tetrahydrocannabinol (THC) at a ratio of 20:1 (a similar ratio as that of hemp-derived full-spectrum CBD oils) to sixty children with confirmed diagnoses of ASD. The dosage was increased to effect a maximum dose of 10mg/kg per day. Efficacy and tolerability were assessed using various questionnaires including a modified Liverpool Adverse Events Profile, the Caregiver Global Impression of Change (CGIC) scale, the Home Situations Questionnaire–Autism Spectrum Disorder (HSQ-ASD) and the Autism Parenting Stress Index (APSI).
Data showed that, following treatment, behavioral outbreaks improved significantly in 61% of patients, anxiety and communication problems improved in 39% and 47% of patients respectively, and disruptive behaviors were improved on average by 29%. In addition, parents reported a reduction in stress. They concluded that this preliminary study provides so much support for the feasibility of CBD as a promising treatment option for refractory behavioral problems in children with ASD, that they have launched a large, double-blind, placebo-controlled cross-over trial with 120 participants.
Oral Cannabidiol Use in Children With Autism Spectrum Disorder to Treat Related Symptoms and Co-morbidities
Reporting on the experiences of parents regarding the effects of oral CBD on co-morbidities such as aggression, hyperactivity and anxiety in their children with ASD, clinicians published their results in Frontiers of Pharmacology in 2019.
In this study, parents of children with autism were instructed to administer a full-spectrum CBD oil with a CBD:THC ratio of 20:1 at a concentration of 30%. The recommended daily dose of CBD was 16 mg/kg (maximum daily dose 600 mg), and for THC- daily dose of 0.8 mg/kg (maximum daily dose of 40 mg) for at least 30 days. The following four ASD co-morbidity symptoms were evaluated: hyperactivity symptoms, sleep problems, self-injury and anxiety using various measures and parental reports.
After objective analysis by an independent group of specialists including a pediatric neurologist specialized in ASD, clinical pharmacologists and pharmacists, results showed that CBD has the potential to improve ASD co-morbidity symptoms significantly. Their study found that, of the 53 children that received CBD for a median of 66 days, self-injury and rage attacks improved by 67.6% in 34 patients, hyperactivity symptoms by 68.4% in 38 children, sleep problems by 71.4% in 21 children and anxiety improved by 47.1% in 17 patients.
The effect of cannabidiol (CBD) on low-frequency activity and functional connectivity in the brain of adults with and without autism spectrum disorder (ASD)
In another 2019 study published in the Journal of Psychopharmacology, this time in adults, scientists investigated the effect of CBD on low-frequency activity and functional connectivity in the brain of individuals with and without ASD.
To investigate this notion, a task-free fMRI was acquired in 17 healthy men and 17 men with ASD. Testing took place following the double-blind oral administration of 600 mg CBD or matched placebo in random order. The fractional amplitude of low-frequency fluctuations (fALFF) in brain activity was measured across the whole brain. In the even of CBD significantly altering fALFF, they also tested if functional connectivity of those regions were also affected by CBD.
Their results showed that results regarding the effects of CBD were primarily driven by the ASD group, showing significantly increased fALFF and functional connectivity in, as well as between cortical regions that are consistently implicated in autism. The researchers concluded that patients with ASD respond differently to CBD, with the implication that it may affect the complex behaviors these regions modulate.
Cannabinoid treatment for autism: a proof-of-concept randomized trial
Currently, there is no established pharmacological method of treating autism spectrum disorders, and the efficacy of drugs in relation to behavioral disorders resulting from ASD is relatively low. Due to the increasing number of reports on the effectiveness of CBD in the treatment of autism spectrum disorders, it was decided to conduct a randomized, double-blind study published in 2021, comparing the effects of two oral solutions (extract of whole cannabis plants and pure cannabinoids) in 150 participants.The participants of the study were children and adolescents (5-21 years) who were diagnosed with ASD due to DSM-5 criteria, having moderate or greater behavioral problems.
It is in this study that the SWOT analysis was applied. After 12 weeks of treatment, there was a 4-week rest period to switch to the second 12-week treatment. The scheme was intended to allow for an analysis within the group of participants, comparing two types of treatment. In order to assess the abnormal behaviour related to ASD, two measurements of indidator results: HSQ-ASD questionnaire nad GCI-Improvement questionnaire in order to assess behavioural problems. The second-tier results involved SRS-2 Scale and APSI-Index. On the CGI-I scale, 49% of the 45 participants who received cannabinoids from whole plants responded (significant or very significant improvement) compared to 21% of the 47 who received placebo (p = 0.005). Of the 45 subjects who received pure cannabinoids, 38% responded to treatment, which was not significantly higher than placebo (p = 0.08). However, an improvement in the total SRS-2 score was noted, which was significantly greater after the use of whole plant extract compared to placebo. The median improvement was 3.6 points after placebo (n = 36) compared to 14.9 points after whole plant extract (n = 34; p = 0.009) and 8.2 points after pure cannabinoids (n = 28; p = 0.80).
In the study described above, it was found that the whole plant extract containing CBD and THC in a ratio of 20:1, improved destructive behavior, which belong to the symptoms resulting from disorders from the autism spectrum. The use of CBD in the treatment of the autism spectrum gives promising results in the area of resistant behavioral problems. These data suggest that cannabinoids should be further investigated in ASD.
Cannabis and cannabinoid use in autism spectrum disorder: a systematic review
Approximately 40% of children struggling with autism spectrum disorders do not respond well to conventional medicine. Standard treatment includes several psychotropic drugs that do not treat ASD but are intended to reduce improper behaviors such as psychomotor arousal or aggression. Therefore, the researchers began to look for alternative therapeutic methods. In 2021, a systematic review of research on the use of cannabinoids in autism spectrum disorders was published.
Out of the 425 articles found, 9 studies were selected for analysis. The review included studies from Israel, England, Brazil, Austria and the United States. Five studies used cannabis extract in the form of CBD-rich oil, while two studies used CBD in the form of an oral solution. One study used dronabinol (a synthetic THC analogue) dissolved in sesame oil, and the last study used cannabidivarin (CBDV). The obtained results of studies using cannabis to improve behaviour indicate a significant reduction in symptoms such as: attacks of self-mutilation and anger, sleep problems, psychomotor arousal, anxiety, aggression. Attention and social interactions have improved.
The results of the analyzed research show that cannabis and cannabinoids can be effective in treating behavioral disorders resulting from ASD. The promising results obtained in this review may be related to the action of phytocannabinoids in cannabis on the regulation of the endocannabinoid system. It is likely that in the future cannabis, CBD or other cannabinoids will be used as a therapeutic alternative in alleviating autistic symptoms.
In addition to the scientific evidence indicating that CBD shows potential for relieving many symptoms of autism as well as those of co-morbidities, anecdotal evidence also shows that CBD may help manage ASD symptoms in some patients. Any search of Facebook groups or Google return 100s, if not 1,000s of results, with many people claiming CBD has helped them, or their child. In addition, online parenting and autism resources are also indicating that there is an upsurge in interest from people interested in using CBD for ASD.
The many properties of CBD has the potential to provide beneficial actions for relieving various aspects, symptoms and co-morbidities in patients with autism. As discussed, CBD may play an important role by, in particular alleviating symptoms of both refractory and disruptive behavioral problems, as well as psychological issues such as anxiety and sleep problems, potentially by changing the cerebral functioning of the brain areas implicated in ASD. However, research is still in its infancy, so it is important to always consult a medical practitioner before using CBD for ASD. Your treating physician or medical specialist can monitor dosage, symptom severity and other clinical parameters including drug interactions and contraindications.
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