Nicotine gene identified

| October 12, 2017

A DNA variant located in the DNMT3B gene and commonly found in people of European and African descent increases the likelihood of developing nicotine dependence, smoking heavily, and developing lung cancer, according to a story on citing a new study led by RTI International.

The story quoted World Health Organization figures claiming that, worldwide, nearly one billion people smoke and six million premature deaths occur annually from cigarette smoking. Smoking was said to be the leading cause of preventable death and one person was said to die every six seconds from smoking-related causes.

The new study, published in Molecular Psychiatry, is said to be the largest genome-wide association study of nicotine dependence. Researchers studied more than 38,600 former and current smokers from the US, Iceland, Finland, and the Netherlands.

“This new finding widens the scope of how genetic factors are known to influence nicotine dependence,” said Dana Hancock, Ph.D., genetic epidemiologist at RTI and co-author of the study.

“The variant that we identified is common, occurring in 44 percent of Europeans or European Americans and 77 percent of African Americans, and it exerts important effects on gene regulation in [the] human brain, specifically in the cerebellum, which has long been overlooked in the study of addiction.”

The genetic variant was linked to an increased risk of nicotine dependence by testing nearly 18 million variants across the genome for association with nicotine dependence. The variant was also tested in independent studies and found to be associated with heavier smoking and with an increased risk of lung cancer.

The story is at:


Category: Breaking News, Science

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