Publications by authors named "M B Chenoweth"

Article Synopsis
  • The nicotine metabolite ratio (NMR) serves as a stable marker for assessing how quickly the body processes nicotine and is useful for customizing smoking cessation efforts.
  • Researchers examined the role of genetic variations in the CYP2A6 gene and their link to NMR in a sample of 953 African American smokers.
  • They discovered several genetic variants associated with NMR, leading to an improved genetic risk score (GRS) that not only predicts NMR in African Americans but also enhances its applicability to smokers of European descent.
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The Pharmacogene Variation Consortium (PharmVar) provides nomenclature for the human CYP2A gene locus containing the highly polymorphic CYP2A6 gene. CYP2A6 plays a role in the metabolism of nicotine and various drugs. Thus, genetic variation can substantially contribute to the function of this enzyme and associated efficacy and safety.

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Varenicline, the most efficacious smoking cessation monotherapy, produces abnormal dreams. Although genetic contributions to varenicline-associated nausea and cessation have been identified, the role of genetics in abnormal dreams is unknown. We conducted a genomewide association study (GWAS) of abnormal dreams in 188 European ancestry smokers treated with varenicline (NCT01314001).

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CYP2A6 is a polymorphic enzyme that inactivates nicotine; structural variants (SVs) include gene deletions and hybrids with the neighboring pseudogene CYP2A7. Two studies found that CYP2A7 deletions were associated with ovarian cancer risk. Using their methodology, we aimed to characterize CYP2A6 SVs (which may be misidentified by prediction software as CYP2A7 SVs), then assess CYP2A6 SV-associated risk for ovarian cancer, and extend analyses to lung cancer.

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