Suppr超能文献

使用遗传/临床风险评分来戒烟(GeTSS):随机对照试验

Using a genetic/clinical risk score to stop smoking (GeTSS): randomised controlled trial.

作者信息

Nichols John A A, Grob Paul, Kite Wendy, Williams Peter, de Lusignan Simon

机构信息

Department of Clinical and Experimental Medicine, University of Surrey, Guildford, Surrey, GU2 7XH, UK.

, 60 Manor Way, Onslow Village, Guildford, Surrey, GU2 7RR, UK.

出版信息

BMC Res Notes. 2017 Oct 23;10(1):507. doi: 10.1186/s13104-017-2831-2.

Abstract

BACKGROUND

As genetic tests become cheaper, the possibility of their widespread availability must be considered. This study involves a risk score for lung cancer in smokers that is roughly 50% genetic (50% clinical criteria). The risk score has been shown to be effective as a smoking cessation motivator in hospital recruited subjects (not actively seeking cessation services).

METHODS

This was an RCT set in a United Kingdom National Health Service (NHS) smoking cessation clinic. Smokers were identified from medical records. Subjects that wanted to participate were randomised to a test group that was administered a gene-based risk test and given a lung cancer risk score, or a control group where no risk score was performed. Each group had 8 weeks of weekly smoking cessation sessions involving group therapy and advice on smoking cessation pharmacotherapy and follow-up at 6 months. The primary endpoint was smoking cessation at 6 months. Secondary outcomes included ranking of the risk score and other motivators.

RESULTS

67 subjects attended the smoking cessation clinic. The 6 months quit rates were 29.4%, (10/34; 95% CI 14.1-44.7%) for the test group and 42.9% (12/28; 95% CI 24.6-61.2%) for the controls. The difference is not significant. However, the quit rate for test group subjects with a "very high" risk score was 89% (8/9; 95% CI 68.4-100%) which was significant when compared with the control group (p = 0.023) and test group subjects with moderate risk scores had a 9.5% quit rate (2/21; 95% CI 2.7-28.9%) which was significantly lower than for above moderate risk score 61.5% (8/13; 95% CI 35.5-82.3; p = 0.03).

CONCLUSIONS

Only the sub-group with the highest risk score showed an increased quit rate. Controls and test group subjects with a moderate risk score were relatively unlikely to have achieved and maintained non-smoker status at 6 months. ClinicalTrials.gov ID NCT01176383 (date of registration: 3 August 2010).

摘要

背景

随着基因检测成本降低,必须考虑其广泛应用的可能性。本研究涉及一种针对吸烟者的肺癌风险评分,其中约50%基于基因(50%基于临床标准)。该风险评分已被证明在医院招募的受试者(并非主动寻求戒烟服务)中作为戒烟激励因素是有效的。

方法

这是一项在英国国民健康服务(NHS)戒烟诊所进行的随机对照试验(RCT)。从医疗记录中识别吸烟者。想要参与的受试者被随机分为试验组,试验组接受基于基因的风险检测并获得肺癌风险评分,或分为对照组,对照组不进行风险评分。每组都有为期8周的每周一次的戒烟课程,包括团体治疗以及关于戒烟药物治疗的建议,并在6个月时进行随访。主要终点是6个月时戒烟。次要结果包括风险评分及其他激励因素的排名。

结果

67名受试者参加了戒烟诊所。试验组6个月戒烟率为29.4%(10/34;95%置信区间14.1 - 44.7%),对照组为42.9%(12/28;95%置信区间24.6 - 61.2%)。差异不显著。然而,风险评分为“非常高”的试验组受试者戒烟率为89%(8/9;95%置信区间68.4 - 100%),与对照组相比具有显著性(p = 0.023),且风险评分为中度的试验组受试者戒烟率为9.5%(2/21;95%置信区间2.7 - 28.9%),显著低于风险评分高于中度的61.5%(8/13;95%置信区间35.5 - 82.3;p = 0.03)。

结论

只有风险评分最高的亚组显示戒烟率有所提高。风险评分为中度的对照组和试验组受试者在6个月时相对不太可能实现并维持不吸烟状态。ClinicalTrials.gov标识符:NCT01176383(注册日期:2010年8月3日)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebaf/5653992/7a853332e39e/13104_2017_2831_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验