Exposure to a common drug for attention deficit hyperactivity disorder (ADHD) isn’t likely to increase cardiovascular risk in healthy kids, according to a new study with monkeys.
With more than 1.8 million children in the US being treated annually with drugs for ADHD, the possibility that such drugs could damage their hearts has been a significant cause of concern for parents and physicians alike. The results of the new, long-term study could allay many of those concerns.
The authors caution that because the study was conducted on primates, the findings are not automatically applicable to humans. However, they have previously published that this primate model reliably shows other side effects similar to those of children receiving these medications. Their new findings conclude that chronic exposure to methylphenidate (MPH), commonly prescribed for ADHD as Ritalin, is unlikely to increase cardiovascular risks in healthy children.
“The findings are very reassuring in that even high-dose chronic MPH stimulant therapy did not result in any evidence of abnormal structures or function in the hearts of the monkeys,” says Steven E. Lipshultz, the study’s principal investigator, and senior and corresponding author, who is professor in and chair of the pediatrics department in the Jacobs School of Medicine and Biomedical Sciences at the University at Buffalo.
Controversy and worry
The results contribute important evidence to an ongoing controversy about whether or not MPH is associated with sudden cardiac death. A number of studies have reported an increase in sudden cardiac death or other damage to the heart in some children taking the drug or other stimulant therapy for ADHD.
“For ethical reasons, this study could not have been done in children.”
With ADHD and related disorders diagnosed in about 10 percent of all children in the US, and with as many as 70 percent of these children receiving stimulant prescription therapy, the question of possible cardiac risks has emerged as a major public health concern, Lipshultz says.
In response, the US Food and Drug Administration has issued a “black box warning” on the drug packaging of some prescription stimulants, noting that children with underlying heart disease should use these medications with caution. Canadian authorities temporarily removed a stimulant drug from use only to reintroduce it, based on the small number of sudden cardiac death events identified through voluntary reporting.
“This controversy has persisted without answer,” says Lipshultz. “Yet the number of prescriptions for these medications for children with ADHD continues to expand.”
For that reason, about a decade ago, Lipshultz was interested to learn of a US government research project involving 30 male rhesus monkeys that had been receiving daily chronic stimulant therapy with MPH. He notes that the monkeys were carefully maintained and ethically cared for at the FDA’s National Center for Toxicological Research in Jefferson, Arkansas.
“I thought they could also shed some light on this charged medical issue related to the safety of chronic stimulant therapy with regard to children’s heart health,” he says.
Lipshultz and his colleagues spent several years developing infrastructure to test how the therapy affected the hearts of these monkeys over the long term. Specialized cardiac catheterization and echocardiography labs were developed at the primate center at the National Center for Toxicological Research where a pediatric interventional cardiologist and a specialist in randomized studies, both on temporary leave from their hospital posts, conducted this study.
For five years, researchers continuously treated the monkeys with therapeutic, super-therapeutic (high doses), or a placebo, using a randomized design, starting when they were about two years old. The duration of the study corresponds to what would be a childhood to adulthood span, the researchers say.
“For ethical reasons, this study could not have been done in children,” says Lipshultz.
After comprehensive cardiovascular assessment in all the monkeys, there were no statistical differences between the three groups on serum cardiovascular and inflammatory biomarkers, electrocardiograms, echocardiograms, cardiac pathology from endomyocardial biopsies, and other clinical parameters.
The single difference of statistical significance was that the researchers found elevated levels of mean serum myoglobin in the lower-dose group. This protein, which is in skeletal and cardiac muscle, can be a sign of skeletal muscle injury when in the serum of humans who have not sustained cardiac injury. Primates in the group receiving high-dose therapy had lower, but still significantly elevated levels.
Because there was no clinical or laboratory evidence of significant cardiac disease in the animals, the authors conclude the elevated myoglobin levels most likely originated in skeletal muscle and were unrelated to a cardiac effect.
In addition to the large population of children being treated with this therapy for ADHD and related disorders, Lipshultz notes that the findings also are good news for child survivors of cancer.
“On a personal level, I have cared for children and adolescents who have survived childhood cancer, who now are experiencing severe learning disabilities as a result of their cancer therapies,” he says. “They become my patients because their hearts have been damaged, an unfortunate effect of the successful treatment of their childhood cancer.
“Current recommendations state that children, such as these, with underlying heart disease should avoid chronic stimulant therapy because of the concern that it could further damage their hearts. However, these prescription stimulants often allow these children to do much better with their learning progress, and denying such a useful therapy for theoretical reasons is difficult. The findings that we are reporting demonstrate that these useful medications, in many cases, can be prescribed to these children as well.”
The research appears in Pediatric Research. Additional coauthors are from Vanderbilt University; the University of Texas; Pro Natural Brands, LLC; the University of Miami; the FDA’s National Center for Toxicological Research; Toxicologic Pathology Associates; and Wayne State University.
The researchers conducted the work while Lipshultz was the chair of pediatrics and director of the Batchelor Children’s Research Institute at the University of Miami Miller School of Medicine, and later while he was the chair of pediatric research at Wayne State University School of Medicine and Children’s Hospital of Michigan.
The Eunice Kennedy Shriver National Institute of Child Health and Human Development of the NIH, the National Center for Toxicological Research, and the FDA funded the study.
Source: University at Buffalo