Alzheimer’s risk does not seem to affect depression, anxiety.
By Kevin Davies
September 15, 2009 | During a panel discussion at last year’s Bio-IT World Expo, the Editor-in-Chief of the New England Journal of Medicine, Jeffrey Drazen, an early skeptic of the predictive power of personal genomics, outlined what steps he needed to see from the genetics community. “I’m from Missouri, and you have to show me,” Drazen said. “You’ve got to do the study that shows that making a difference in [genetic] knowledge will make a difference in how people behave.”
Drazen added, “We’re not there yet… I wish you good luck, and send me your papers when you show that it works!” Sitting in the audience, Boston University neurologist Robert Green gladly seized the opening and informed Drazen he was preparing to submit just such a manuscript.
That paper, presenting the findings of the REVEAL (Risk Evaluation and Education for Alzheimer’s Disease) study, was published in the Journal in July. It represents a milestone in judging the public’s attitude to—and ability to cope with—the sometimes adverse results of personal genetic testing.
Green’s group set out to examine attitudes of people with a family history of Alzheimer’s disease to learning their all-important APOE genotype. The apolipoprotein E (APOE) gene on chromosome 19 is a well-known predictor of Alzheimer’s risk. Individuals who inherit one copy of the e4 allele have a 2-3 fold relative risk of the disease, whereas e4 homozygotes have around a 15-fold greater risk.
The study was actually performed between 2000 and 2003. Green and his colleagues enrolled 162 adults who had one or both parents diagnosed with AD. All received counseling information before the trial began. 111 were told their APOE genotype, whereas 51 remained as controls in the nondisclosure group. Of the 111 individuals tested, 53 were heterozygous or homozygous for the e4 allele.
Green and colleagues found few if any differences between the two groups with regard to the individuals’ levels of anxiety, depression or distress, even up to one year after the study. “Subjects who learned they were e4 positive… showed no more anxiety, depression or test-related distress than those who did not learn their genotype,” the authors write. (There was a slight short-term but transient increase in anxiety in the e4 group.) The individuals that showed the most dramatic, or clinically meaningful, changes in psychological profile were spread evenly between the control group and the disclosure group (regardless of e4 carrier status).
Despite the lengthy genesis of the study, there are inevitably shortcomings. As Green et al. note, “If APOE genotyping had been provided without genetic counseling or to subjects who had no family history of Alzheimer’s disease, the results might have been different. In addition, the exclusion of subjects with low neurocognitive scores and high depression scores may have influenced the results.”
While advocating more expansive follow-up studies, nevertheless, Green’s team draws satisfaction from the REVEAL findings that disclosing genotyping information to individuals who test negative is beneficial, and causes only transient, modest distress to those who end up testing positive. “These data support the psychological safety of disclosing data regarding genetic-counseling protocols” to Alzheimer’s family members, “despite the frightening nature of the disease and the fact that the disclosure has no clear medical benefit.”
*Green, R.C. et al. “Disclosure of APOE genotype for risk of Alzheimer’s disease.” New England Journal of Medicine 361, 245-254; July 16 2009.
This article also appeared in the September-October 2009 issue of Bio-IT World Magazine.
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