Family history does not influence stress or major coping styles in adults with neurofibromatosis type 1

IF 1.9 4区 医学 Q3 GENETICS & HEREDITY
Mikaela Bradley, Ashley Cannon, Bryce Brown, Kelly Taylor, Paul Moots, Emily McQuillen
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引用次数: 0

Abstract

Neurofibromatosis type 1 (NF1) is a genetic condition that affects about 1 in 3000 individuals. Approximately 50% of individuals with NF1 have a family history of the condition. Individuals with NF1 experience variable symptoms that contribute to increased stress. This study investigated whether a family history of NF1 influences levels of stress and coping strategies in adults with NF1. Adults with NF1 who live in the United States and speak English were recruited through the Children's Tumor Foundation's (CTF) NF Registry, CTF's NF Clinic Network, and the Neurofibromatosis Network. Participants completed a survey about their personal and family history of NF1, the Perceived Stress Scale 10-Item Version (PSS-10), the Brief Coping Orientation to Problems Experienced Inventory (Brief-COPE), short response questions, and demographics. Overall, 547 of 646 responses met analysis criteria. Participants with affected parents were assigned to the inherited NF1 group (n = 222) and those with unaffected parents were assigned to the sporadic NF1 group (n = 325). No differences were found in mean PSS-10 scores between the two study groups (p = 0.568). Females had significantly higher PSS-10 scores than males (p < 0.001). After Bonferroni correction, no differences were found across Brief-COPE subscales or major coping styles between the two groups. A stagewise multivariable regression indicated that 42% of the variance in PSS-10 scores was accounted for by sex assigned at birth, age, problem-focused, and avoidant coping styles (R2 = 0.42, p < 0.001). Family history did not predict PSS-10 scores alone or as an interaction variable with major coping styles. This study showed no significant differences in stress or major coping styles between adults with inherited versus sporadic NF1. However, other factors may influence the stress and coping experiences of adults with NF1. Fostering discussions about patients' stressors and coping strategies could help promote stress management.

家族史不影响成人1型神经纤维瘤病的压力或主要应对方式
1型神经纤维瘤病(NF1)是一种遗传病,大约每3000人中就有1人患病。大约50%的NF1患者有家族病史。患有NF1的个体经历不同的症状,导致压力增加。本研究调查了NF1家族史是否会影响NF1成人的压力水平和应对策略。通过儿童肿瘤基金会(CTF)的NF登记处、CTF的NF临床网络和神经纤维瘤病网络招募了居住在美国并说英语的NF1成人。参与者完成了一项关于NF1的个人和家族史的调查,感知压力量表10项版本(PSS-10),问题经验的简短应对取向量表(Brief- cope),简短回答问题和人口统计。总体而言,646个回复中有547个符合分析标准。父母受感染的参与者被分配到遗传性NF1组(n = 222),父母未受影响的参与者被分配到散发性NF1组(n = 325)。两组患者PSS-10平均评分无差异(p = 0.568)。女性的PSS-10得分显著高于男性(p < 0.001)。经Bonferroni校正后,两组在Brief-COPE子量表或主要应对方式上均无差异。分阶段多变量回归表明,PSS-10得分的42%的差异是由出生时的性别、年龄、问题焦点和回避型应对方式造成的(R2 = 0.42, p < 0.001)。家族史不能单独预测PSS-10得分,也不能作为主要应对方式的交互变量。该研究显示,成人遗传NF1与散发性NF1在压力或主要应对方式上没有显著差异。然而,其他因素可能影响NF1成人的压力和应对经验。促进对患者压力源和应对策略的讨论有助于促进压力管理。
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来源期刊
Journal of Genetic Counseling
Journal of Genetic Counseling GENETICS & HEREDITY-
CiteScore
3.80
自引率
26.30%
发文量
113
审稿时长
6 months
期刊介绍: The Journal of Genetic Counseling (JOGC), published for the National Society of Genetic Counselors, is a timely, international forum addressing all aspects of the discipline and practice of genetic counseling. The journal focuses on the critical questions and problems that arise at the interface between rapidly advancing technological developments and the concerns of individuals and communities at genetic risk. The publication provides genetic counselors, other clinicians and health educators, laboratory geneticists, bioethicists, legal scholars, social scientists, and other researchers with a premier resource on genetic counseling topics in national, international, and cross-national contexts.
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