Weinberg David S, Myers Ronald E, Keenan Eileen, Ruth Karen, Sifri Randa, Ziring Barry, Ross Eric, Manne Sharon L
Ann Intern Med. 2014 Oct 21;161(8):537-45. doi: 10.7326/M14-0765.
New methods are needed to improve health behaviors, such as adherence to colorectal cancer (CRC) screening. Personalized genetic information to guide medical decisions is increasingly available. Whether such information motivates behavioral change is unknown.
To determine whether individualized genetic and environmental risk assessment (GERA) of CRC susceptibility improves adherence to screening in average-risk persons.
2-group, randomized, controlled trial. (ClinicalTrials.gov: NCT0087360).
4 medical school-affiliated primary care practices.
783 participants at average risk for CRC who were not adherent to screening at study entry.
Participants were randomly assigned to usual care or GERA, which evaluated methylenetetrahydrofolate reductase polymorphisms and serum folate levels. On the basis of prespecified combinations of polymorphisms and serum folate levels, GERA recipients were told that they were at elevated or average risk for CRC.
The primary outcome was CRC screening within 6 months of study entry.
Overall screening rates for CRC did not statistically significant differ between the usual care (35.7%) and GERA (33.1%) groups. After adjustment for baseline participant factors, the odds ratio for screening completion for GERA versus usual care was 0.88 (95% CI, 0.64 to 1.22). Within the GERA group, screening rates did not significantly differ between average-risk (38.1%) and elevated-risk (26.9%) participants. Odds ratios for elevated- versus average-risk participants remained nonsignificant after adjustment for covariates (odds ratio, 0.75 [CI, 0.39 to 1.42]).
Only 1 personalized genetic and environmental interaction and 1 health behavior (CRC screening) were assessed.
In average-risk persons, CRC screening uptake was not positively associated with feedback from a single personalized GERA. Additional studies will be required to evaluate whether other approaches to providing GERA affect screening utilization differently. These findings raise concern about the effectiveness of moderately predictive assessment of genetic risk to promote favorable health care behavior.
National Institutes of Health.
需要新方法来改善健康行为,如坚持进行结直肠癌(CRC)筛查。用于指导医疗决策的个性化基因信息越来越多。但此类信息是否能促使行为改变尚不清楚。
确定结直肠癌易感性的个体化基因和环境风险评估(GERA)是否能提高平均风险人群的筛查依从性。
两组随机对照试验。(ClinicalTrials.gov注册号:NCT0087360)。
4家医学院附属的初级保健机构。
783名结直肠癌平均风险参与者,研究开始时未坚持进行筛查。
参与者被随机分配至常规护理组或GERA组,后者评估亚甲基四氢叶酸还原酶多态性和血清叶酸水平。根据多态性和血清叶酸水平的预先设定组合,GERA组参与者被告知其患结直肠癌的风险升高或处于平均水平。
主要结局为研究开始后6个月内进行结直肠癌筛查。
常规护理组(35.7%)和GERA组(33.1%)的总体结直肠癌筛查率在统计学上无显著差异。在对基线参与者因素进行调整后,GERA组与常规护理组完成筛查的比值比为0.88(95%CI,0.64至1.22)。在GERA组中,平均风险参与者(38.1%)和高风险参与者(26.9%)的筛查率无显著差异。在对协变量进行调整后,高风险与平均风险参与者的比值比仍无统计学意义(比值比,0.75[CI,0.39至1.42])。
仅评估了1种个性化基因与环境的相互作用和1种健康行为(结直肠癌筛查)。
在平均风险人群中,结直肠癌筛查接受率与单一的个性化GERA反馈无正相关。需要进一步研究来评估提供GERA的其他方法是否对筛查利用率有不同影响。这些发现引发了对基因风险适度预测评估促进有利医疗行为有效性的担忧。
美国国立卫生研究院。