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PLoS One. 2012;7(7):e40230. doi: 10.1371/journal.pone.0040230. Epub 2012 Jul 11.

Impact of genetic notification on smoking cessation: systematic review and pooled-analysis.

Author information

1
Operational Direction Public Health and Surveillance, Scientific Institute of Public Health, Brussels, Belgium. Sylviane.deviron@wiv-isp.be

Abstract

OBJECTIVES:

This study aimed to evaluate the impact of genetic notification of smoking-related disease risk on smoking cessation in the general population. Secondary objectives were to assess the impact of genetic notification on intention-to-quit smoking and on emotional outcomes as well as the understanding and the recall of this notification.

METHODS:

A systematic review of articles from inception to August 2011 without language restriction was realized using PubMed, Embase, Scopus, Web of Science, PsycINFO and Toxnet. Other publications were identified using hand search. The pooled-analysis included only randomized trials. Comparison groups were (i) high and low genetic risk versus control, and (ii) high versus low genetic risk. For the pooled-analysis random effect models were applied and sensitivity analyses were conducted.

RESULTS:

Eight papers from seven different studies met the inclusion criteria of the review. High genetic risk notification was associated with short-term increased depression and anxiety. Four randomized studies were included in the pooled-analysis, which revealed a significant impact of genetic notification on smoking cessation in comparison to controls (clinical risk notification or no intervention) in short term follow-up less than 6 months (RR = 1.55, 95% CI 1.09-2.21).

CONCLUSIONS:

In short term follow-up, genetic notification increased smoking cessation in comparison to control interventions. However, there is no evidence of long term effect (up to 12 month) on smoking cessation. Further research is needed to assess more in depth how genetic notification of smoking-related disease could contribute to smoking cessation.

PMID:
22808123
PMCID:
PMC3394798
DOI:
10.1371/journal.pone.0040230
[Indexed for MEDLINE]
Free PMC Article

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