Parents are going where scientists fear to tread to calm their children’s autism and epilepsy symptoms.
Jessica WrightSpencer, her boy, was having increasingly aggressive tantrums, and was becoming harder to control. By the age of 11, he was lashing out with “run-by slappings” of his sisters, and threatening to take his own life and his parents’. Terrified that his aggression might force the family to consider other housing options, Karlee turned to marijuana two years ago, cast as a miracle cure in an internet success story she had read. She suspected the story was “baloney,” but she was desperate.
Meanwhile, neurologist Gregory Barnes keeps his marijuana derivative inside a lockbox, stored inside a biometric safe, inside a locked pharmacy. This year, Barnes plans to start the first clinical trial to test the effect of cannabidivarin (CBDV) on children who have both autism and epilepsy.
In 2011, the then-governors of Rhode Island and Washington petitioned the DEA to reclassify medical marijuana as a Schedule 2 drug. The change would have enabled states to regulate safe access to medical marijuana for those who need it without violating federal law. But in August, the DEA reaffirmed its stance, based on a recommendation by the Food and Drug Administration (FDA) and the National Institute on Drug Abuse. The DEA did relax some rules, however, inviting universities to apply to grow marijuana for “research purposes.”
These stark contrasts leave the state of marijuana research for autism in a bizarre state of flux: Marijuana is simultaneously legal and illegal, easy to obtain and heavily restricted, a miracle cure and a completely untested treatment navigating the first rounds of clinical trials.
At the crux of the contradictions lie important questions: Is marijuana a legitimate treatment for autism? And is it safe to give to children? Many families feel they already know the answers. But researchers say these questions need to be addressed in a controlled, rigorous way.
California became the first U.S. state to legalize medical marijuana, mainly for adults with severe chronic illness such as cancer or AIDS. Since California’s decision in 1996, 24 states and the District of Columbia (Washington, D.C.) have followed, and since 2012, four states and Washington, D.C., have legalized recreational use of the drug. So far, only Pennsylvania specifically permits medical marijuana use for autism, but in the past few years, parents of children with epilepsy across the nation have adopted this approach.
Much of this enthusiasm stemmed from the widespread media coverage in 2013 of Charlotte’s Web, a marijuana strain with high levels of CBD. The strain reportedly helped its namesake, Charlotte—a young girl with a form of epilepsy called Dravet syndrome—go from having hundreds of seizures a week to being practically seizure-free.
Giving her son marijuana was not an easy decision for Karlee. “Growing up, it was: ‘Drugs are bad, drugs are bad, marijuana is terrible, it’s a gateway drug for heroin and meth and so on,’” she says. “I still have that wrestle in my head thinking, 'Oh my gosh, you’re doing it to get him high.’” Ultimately, she says, she realized that if she didn’t give him marijuana, she’d end up giving him something even more dangerous.
With her prescription in hand, Karlee was able to visit a for-profit medical dispensary that sells marijuana oils and tinctures—marijuana extracts steeped in alcohol. At these dispensaries, customers are greeted by a bewildering variety of choices. Marijuana includes a mix of hundreds of bioactive compounds, and plant breeders have created hundreds of strains, each of which harbors a different proportion of these chemicals.
Families must choose a strain based mainly on the dispensaries’ advice or on internet lore—a fact that makes some researchers extremely nervous. “I worry a lot about a physician sending a child, or a child’s parents, to a dispensary to have a conversation about what type and dose and route of administration of cannabis should be given to a kid,” says Ryan Vandrey, associate professor of behavioral sciences at Johns Hopkins University in Baltimore. “To me, that’s completely backwards,” he says. Vandrey studies the effects of marijuana exposure on adults.
Spencer responds best to tinctures that contain roughly a 3-to-5 ratio of THC to CBD, Karlee says. She continually experiments with this ratio, and when and how often to dose, to find the most effective treatment. As Spencer has grown, she has needed to give him more and more of the compounds. To counteract his rising tolerance, she sometimes tapers the drug concentration down for a week, then raises it back up. She has also used a high-THC oil at night to help Spencer sleep.
This
option is not available to Leslie Johnson, who lives in New Jersey and
gives medical marijuana to her adult son, John, to help him cope with
severe epilepsy and autism. Devinsky prescribed marijuana for Johnson’s
son in January 2015 after a seizure medication lowered John’s white
blood cell count to a dangerous point. But New Jersey permits
dispensaries to sell only the dried plant, lozenges, and topical
treatments. So Johnson has to figure out how to turn the plant into
something more appropriate than a joint to give to her son. “I have no
idea why New Jersey came up with their policy,” says Devinsky.
Still, the drug has worked better than she expected, Johnson says. Her son became calmer and more content after the first 1-milliliter dose. During the year and a half he has used the drug, Johnson has lowered the dosage of his seizure medications significantly. She says he has had, at most, three severe seizures, compared with at least one per month before. In the past few months, she has been experimenting with strains that have slightly more THC, which she says seems to have the best calming effect. “You do anything you can for your son, if it’s going to help him,” she says. “Mothers like me, we consider ourselves pioneers in this. We’re the newbies.”
Marijuana’s effects on a child who takes it regularly are unknown. Many parents assume the drug is safe simply because they have taken it themselves, but occasional use by a young adult is not the same as a child taking it daily for years. In fact, little is known about how the chemicals it contains work in the brain at all. In a 2013 study, researchers in Italy reported that blocking the CB1 receptor alleviates seizures as well as memory problems in a mouse model of fragile X syndrome, an autism-related condition.
Most studies in people have looked at the effects of long-term marijuana use as a recreational drug, and raise some concerns. A 2012 study showed that 19 recreational marijuana users who began smoking before age 16 had problems with cognitive function. A 2014 study by the same team found changes in brain connectivity that tracked with impulsiveness in 25 regular marijuana smokers. Another study followed more than 1,000 people from birth to 38 years of age and found that those who used marijuana regularly as adolescents showed a decline in their intelligence quotients in adulthood.
Jeste does not endorse the use of marijuana, but makes sure she knows if children are taking it, so she can try to track its effects with other medications she prescribes. She says she understands parents’ desperate search for something that might work. These parents urgently need research that can guide them through their choices, she says. “It's our job to do the trials. I'm not going to say, ‘Oh there's no evidence, I’m just going to pooh-pooh the whole thing,’” she says. “We need to do studies.”
Intrigued by this evidence, in 2014, Hussain launched his ‘upside-down’ clinical trial—in which research follows widespread use rather than the other way around. He did an online survey of the parents of 117 children who were trying high-CBD marijuana strains to curb their child’s epilepsy.
Devinsky and his colleagues tested a new CBD compound made by GW in nearly 200 children and adults across 11 epilepsy centers in the U.S. The participants all had severe childhood epilepsy that had not responded to conventional treatment. By the end of the trial, 20 of the participants were free of seizures. But 20 participants had severe side effects, such as diarrhea and nausea; 9 of them showed a dangerous spike in seizure frequency called ‘status epilepticus’ that may have stemmed from the drug. The trial was open-label, meaning that participants knew what they were taking and why—so it’s possible these reports were influenced by a placebo effect.
In the meantime, GW has been conducting a clinical trial that is yielding promising results. The company reported in March that in a late-stage trial, its CBD compound Epidiolex reduced the frequency of seizures by 39 percent in 60 participants with Dravet syndrome.
One of the challenges when designing marijuana studies for autism will be finding a way to objectively measure these anecdotal observations, Jeste says. “Are we trying to improve social communication, are we trying to improve sleep, are we trying to improve irritability? What are we trying to move?”
Hussain says he knew setting up his clinical trial would be difficult, but it proved even more challenging than he had expected. Apart from getting the DEA’s permission, he had to have his protocol approved by the California State Department of Justice and the FDA. He also needed to navigate university politics, convincing staff there that the study would be legal, and wouldn’t damage their reputation.
“You need buy-in from your colleagues who are helping you recruit patients—who are helping you conduct studies; you need buy-in from your department at your university; you need buy-in from the university-wide establishment; you need buy-in from the legal folks at your university,” he says. “As this goes forward, you keep getting new layers of bureaucracy.”
Hussain says that on his own, the barriers might have seemed unnavigable. He and Barnes both got help from their pharmaceutical company partners, which provided their compounds as well as consultants for the mess of federal forms. Researchers without pharma partners must apply to receive marijuana through the federal government. The entire federal supply comes from a single site at the University of Mississippi in Oxford, although the new DEA policy may change that. Last year, the government approved 23 requests for marijuana for research projects.
Parents, meanwhile, are continuing to lead the way in testing marijuana. When Barnes was involved in the Dravet syndrome trial, he was deluged with calls from parents eager to enroll their children. He anticipates getting as many as five calls a day for the 10 spots in his autism trial.
Some parents aren’t waiting for trials. Karlee has a permit to grow marijuana in her backyard, so she no longer has to drive for hours to a dispensary. But when Washington state legalized the sale of recreational marijuana in July 2014, it also tightened restrictions on dispensaries and on individuals growing the plant. “We’re trying to make sure we’re obeying the law, but it’s a little vague,” Karlee says.
Last year, Karlee harvested enough marijuana to provide oil for Spencer for the entire year. In the next few weeks, she will be starting her second harvest, stripping the plant’s leaves to make the medicine she says changed everything for her family.
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