Modifiable risk factors for cancer among people with lynch syndrome: an international, cross-sectional survey.

IF 2 4区 医学 Q3 ONCOLOGY Hereditary Cancer in Clinical Practice Pub Date : 2024-06-14 DOI:10.1186/s13053-024-00280-w
Robert F Power, Damien E Doherty, Roberta Horgan, Pat Fahey, David J Gallagher, Maeve A Lowery, Karen A Cadoo
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Abstract

Background: Lynch syndrome is the most common cause of hereditary colorectal and endometrial cancer. Lifestyle modification may provide an opportunity for adjunctive cancer prevention. In this study, we aimed to characterise modifiable risk factors in people with Lynch syndrome and compare this with international guidelines for cancer prevention.

Methods: A cross-sectional study was carried out utilizing survey methodology. Following public and patient involvement, the survey was disseminated through patient advocacy groups and by social media. Self-reported demographic and health behaviours were collected in April 2023. Guidelines from the World Cancer Research Fund (WCRF) were used to compare percentage adherence to 9 lifestyle recommendations, including diet, physical activity, weight, and alcohol intake. Median adherence scores, as a surrogate for lifestyle risk, were calculated and compared between groups.

Results: 156 individuals with Lynch syndrome participated from 13 countries. The median age was 51, and 54% were cancer survivors. The mean BMI was 26.7 and the mean weekly duration of moderate to vigorous physical activity was 90 min. Median weekly consumption of ethanol was 60 g, and 3% reported current smoking. Adherence to WCRF recommendations for cancer prevention ranged from 9 to 73%, with all but one recommendation having < 50% adherence. The median adherence score was 2.5 out of 7. There was no significant association between median adherence scores and age (p = 0.27), sex (p = 0.31), or cancer history (p = 0.75).

Conclusions: We have characterised the modifiable risk profile of people living with Lynch syndrome, outlining targets for intervention based on lifestyle guidelines for the general population. As evidence supporting the relevance of modifiable factors in Lynch syndrome emerges, behavioural modification may prove an impactful means of cancer prevention.

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林奇综合征患者中可改变的癌症风险因素:一项国际横断面调查。
背景:林奇综合征是遗传性结直肠癌和子宫内膜癌最常见的病因。改变生活方式可为辅助预防癌症提供机会。在这项研究中,我们旨在了解林奇综合征患者的可改变风险因素,并将其与国际癌症预防指南进行比较:方法:我们采用调查方法开展了一项横断面研究。在公众和患者的参与下,调查通过患者权益团体和社交媒体进行传播。于 2023 年 4 月收集了自我报告的人口统计和健康行为。调查采用了世界癌症研究基金会(WCRF)的指南,比较了9种生活方式建议(包括饮食、体育锻炼、体重和酒精摄入量)的遵守比例。作为生活方式风险的替代指标,计算并比较了各组的坚持率中位数:结果:来自 13 个国家的 156 名林奇综合征患者参与了研究。中位年龄为 51 岁,54% 为癌症幸存者。平均体重指数为 26.7,每周中等强度至剧烈运动的平均持续时间为 90 分钟。每周乙醇摄入量的中位数为 60 克,3% 的人表示目前正在吸烟。世界癌症研究基金会提出的癌症预防建议的采纳率从 9% 到 73% 不等,除一项建议外,其他建议均有结论:我们描述了林奇综合征患者的可改变风险特征,并根据普通人群的生活方式指南概述了干预目标。随着支持林奇综合征可改变因素相关性的证据的出现,行为改变可能会被证明是一种有效的癌症预防手段。
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来源期刊
CiteScore
3.10
自引率
5.90%
发文量
38
审稿时长
>12 weeks
期刊介绍: Hereditary Cancer in Clinical Practice is an open access journal that publishes articles of interest for the cancer genetics community and serves as a discussion forum for the development appropriate healthcare strategies. Cancer genetics encompasses a wide variety of disciplines and knowledge in the field is rapidly growing, especially as the amount of information linking genetic differences to inherited cancer predispositions continues expanding. With the increased knowledge of genetic variability and how this relates to cancer risk there is a growing demand not only to disseminate this information into clinical practice but also to enable competent debate concerning how such information is managed and what it implies for patient care. Topics covered by the journal include but are not limited to: Original research articles on any aspect of inherited predispositions to cancer. Reviews of inherited cancer predispositions. Application of molecular and cytogenetic analysis to clinical decision making. Clinical aspects of the management of hereditary cancers. Genetic counselling issues associated with cancer genetics. The role of registries in improving health care of patients with an inherited predisposition to cancer.
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