Hamilton Jada G, Hutson Sadie P, Frohnmayer Amy E, Han Paul K J, Peters June A, Carr Ann G, Alter Blanche P
Department of Psychiatry & Behavioral Sciences, Memorial Sloan Kettering Cancer Center, 641 Lexington Avenue, 7th floor, New York, NY, 10022, USA.
College of Nursing, University of Tennessee-Knoxville, Knoxville, TN, USA.
J Genet Couns. 2015 Oct;24(5):760-70. doi: 10.1007/s10897-014-9807-3. Epub 2014 Dec 27.
Inherited bone marrow failure syndromes (IBMFS) including Fanconi anemia, dyskeratosis congenita, Diamond-Blackfan anemia, and Shwachman-Diamond syndrome are rare genetic disorders characterized by hematologic complications and increased risk of cancer. Patients and their families likely experience obstacles in obtaining sufficient health information given their disorders' rarity. To investigate this possibility, we examined information-seeking behaviors and levels of general and disorder-specific genetic knowledge among 315 members of 174 families with an IBMFS, and how information-seeking behaviors and socio-demographic factors may be associated with their genetic knowledge. Cross-sectional survey data indicated that participants were most likely to have ever used the Internet or healthcare providers for genetic information. On average, participants correctly answered 57 % of items assessing general genetic knowledge and 49-59 % of disorder-specific knowledge items. Greater knowledge was associated with greater education and ever experiencing genetic counseling, attending a scientific meeting, and seeking information from the Internet and scientific literature. Among families with Fanconi anemia (whose family support organization has the longest history of providing information), greater disorder-specific genetic knowledge was also associated with seeking information from support groups and other affected families. Results suggest that families with IBMFS have uncertainty regarding genetic aspects of their disorder, and highlight potential channels for delivering educational resources.
遗传性骨髓衰竭综合征(IBMFS),包括范可尼贫血、先天性角化不良、先天性纯红细胞再生障碍性贫血和施-戴综合征,是罕见的遗传性疾病,其特征为血液学并发症和癌症风险增加。鉴于这些疾病的罕见性,患者及其家属在获取足够的健康信息方面可能会遇到障碍。为了调查这种可能性,我们研究了174个患有IBMFS的家庭的315名成员的信息寻求行为以及一般和疾病特异性遗传知识水平,以及信息寻求行为和社会人口学因素如何与他们的遗传知识相关联。横断面调查数据表明,参与者最有可能通过互联网或医疗服务提供者获取遗传信息。平均而言,参与者正确回答了评估一般遗传知识项目的57%以及疾病特异性知识项目的49%-59%。更多的知识与更高的教育程度以及曾接受遗传咨询、参加科学会议、从互联网和科学文献中获取信息有关。在患有范可尼贫血的家庭中(其家庭支持组织提供信息的历史最长),更多的疾病特异性遗传知识也与从支持小组和其他受影响家庭获取信息有关。结果表明,患有IBMFS的家庭对其疾病的遗传方面存在不确定性,并突出了提供教育资源的潜在渠道。