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Effect of communicating DNA based risk assessments for Crohn’s disease on smoking cessation: randomised controlled trial

Objective To test the hypothesis that communicating risk of developing Crohn’s disease based on genotype and that stopping smoking can reduce this risk, motivates behaviour change among smokers at familial risk. Design Parallel group, cluster randomised controlled trial. Setting Families with Crohn’...

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Autores principales: Hollands, Gareth J, Whitwell, Sophia C L, Parker, Richard A, Prescott, Natalie J, Forbes, Alastair, Sanderson, Jeremy, Mathew, Christopher G, Lewis, Cathryn M, Watts, Sally, Sutton, Stephen, Armstrong, David, Kinmonth, Ann Louise, Prevost, A Toby, Marteau, Theresa M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group Ltd. 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3401124/
https://www.ncbi.nlm.nih.gov/pubmed/22822007
http://dx.doi.org/10.1136/bmj.e4708
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author Hollands, Gareth J
Whitwell, Sophia C L
Parker, Richard A
Prescott, Natalie J
Forbes, Alastair
Sanderson, Jeremy
Mathew, Christopher G
Lewis, Cathryn M
Watts, Sally
Sutton, Stephen
Armstrong, David
Kinmonth, Ann Louise
Prevost, A Toby
Marteau, Theresa M
author_facet Hollands, Gareth J
Whitwell, Sophia C L
Parker, Richard A
Prescott, Natalie J
Forbes, Alastair
Sanderson, Jeremy
Mathew, Christopher G
Lewis, Cathryn M
Watts, Sally
Sutton, Stephen
Armstrong, David
Kinmonth, Ann Louise
Prevost, A Toby
Marteau, Theresa M
author_sort Hollands, Gareth J
collection PubMed
description Objective To test the hypothesis that communicating risk of developing Crohn’s disease based on genotype and that stopping smoking can reduce this risk, motivates behaviour change among smokers at familial risk. Design Parallel group, cluster randomised controlled trial. Setting Families with Crohn’s disease in the United Kingdom. Participants 497 smokers (mean age 42.6 (SD 14.4) years) who were first degree relatives of probands with Crohn’s disease, with outcomes assessed on 209/251 (based on DNA analysis) and 217/246 (standard risk assessment). Intervention Communication of risk assessment for Crohn’s disease by postal booklet based on family history of the disease and smoking status alone, or with additional DNA analysis for the NOD2 genotype. Participants were then telephoned by a National Health Service Stop Smoking counsellor to review the booklet and deliver brief standard smoking cessation intervention. Calls were tape recorded and a random subsample selected to assess fidelity to the clinical protocol. Main outcome measure The primary outcome was smoking cessation for 24 hours or longer, assessed at six months. Results The proportion of participants stopping smoking for 24 hours or longer did not differ between arms: 35% (73/209) in the DNA arm versus 36% (78/217) in the non-DNA arm (difference −1%, 95% confidence interval −10% to 8%, P=0.83). The proportion making a quit attempt within the DNA arm did not differ between those who were told they had mutations putting them at increased risk (36%), those told they had none (35%), and those in the non-DNA arm (36%). Conclusion Among relatives of patients with Crohn’s disease, feedback of DNA based risk assessments does not motivate behaviour change to reduce risk any more or less than standard risk assessment. These findings accord with those across a range of populations and behaviours. They do not support the promulgation of commercial DNA based tests nor the search for gene variants that confer increased risk of common complex diseases on the basis that they effectively motivate health related behaviour change. Trial registration Current Controlled Trials ISRCTN21633644.
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spelling pubmed-34011242012-07-25 Effect of communicating DNA based risk assessments for Crohn’s disease on smoking cessation: randomised controlled trial Hollands, Gareth J Whitwell, Sophia C L Parker, Richard A Prescott, Natalie J Forbes, Alastair Sanderson, Jeremy Mathew, Christopher G Lewis, Cathryn M Watts, Sally Sutton, Stephen Armstrong, David Kinmonth, Ann Louise Prevost, A Toby Marteau, Theresa M BMJ Research Objective To test the hypothesis that communicating risk of developing Crohn’s disease based on genotype and that stopping smoking can reduce this risk, motivates behaviour change among smokers at familial risk. Design Parallel group, cluster randomised controlled trial. Setting Families with Crohn’s disease in the United Kingdom. Participants 497 smokers (mean age 42.6 (SD 14.4) years) who were first degree relatives of probands with Crohn’s disease, with outcomes assessed on 209/251 (based on DNA analysis) and 217/246 (standard risk assessment). Intervention Communication of risk assessment for Crohn’s disease by postal booklet based on family history of the disease and smoking status alone, or with additional DNA analysis for the NOD2 genotype. Participants were then telephoned by a National Health Service Stop Smoking counsellor to review the booklet and deliver brief standard smoking cessation intervention. Calls were tape recorded and a random subsample selected to assess fidelity to the clinical protocol. Main outcome measure The primary outcome was smoking cessation for 24 hours or longer, assessed at six months. Results The proportion of participants stopping smoking for 24 hours or longer did not differ between arms: 35% (73/209) in the DNA arm versus 36% (78/217) in the non-DNA arm (difference −1%, 95% confidence interval −10% to 8%, P=0.83). The proportion making a quit attempt within the DNA arm did not differ between those who were told they had mutations putting them at increased risk (36%), those told they had none (35%), and those in the non-DNA arm (36%). Conclusion Among relatives of patients with Crohn’s disease, feedback of DNA based risk assessments does not motivate behaviour change to reduce risk any more or less than standard risk assessment. These findings accord with those across a range of populations and behaviours. They do not support the promulgation of commercial DNA based tests nor the search for gene variants that confer increased risk of common complex diseases on the basis that they effectively motivate health related behaviour change. Trial registration Current Controlled Trials ISRCTN21633644. BMJ Publishing Group Ltd. 2012-07-20 /pmc/articles/PMC3401124/ /pubmed/22822007 http://dx.doi.org/10.1136/bmj.e4708 Text en © Hollands et al 2012 This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/2.0/ and http://creativecommons.org/licenses/by-nc/2.0/legalcode.
spellingShingle Research
Hollands, Gareth J
Whitwell, Sophia C L
Parker, Richard A
Prescott, Natalie J
Forbes, Alastair
Sanderson, Jeremy
Mathew, Christopher G
Lewis, Cathryn M
Watts, Sally
Sutton, Stephen
Armstrong, David
Kinmonth, Ann Louise
Prevost, A Toby
Marteau, Theresa M
Effect of communicating DNA based risk assessments for Crohn’s disease on smoking cessation: randomised controlled trial
title Effect of communicating DNA based risk assessments for Crohn’s disease on smoking cessation: randomised controlled trial
title_full Effect of communicating DNA based risk assessments for Crohn’s disease on smoking cessation: randomised controlled trial
title_fullStr Effect of communicating DNA based risk assessments for Crohn’s disease on smoking cessation: randomised controlled trial
title_full_unstemmed Effect of communicating DNA based risk assessments for Crohn’s disease on smoking cessation: randomised controlled trial
title_short Effect of communicating DNA based risk assessments for Crohn’s disease on smoking cessation: randomised controlled trial
title_sort effect of communicating dna based risk assessments for crohn’s disease on smoking cessation: randomised controlled trial
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3401124/
https://www.ncbi.nlm.nih.gov/pubmed/22822007
http://dx.doi.org/10.1136/bmj.e4708
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