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用于评估 Prader-Willi 综合征患者行为的疾病特异性问卷。

A disease specific questionnaire for assessing behavior in individuals with Prader-Willi syndrome.

机构信息

PWS Multidisciplinary Clinic, Neuropediatric Unit, Shaare Zedek Medical Center, POB 3235, Jerusalem 9103102, Israel.

School of Education, The Hebrew University of Jerusalem, Mount Scopus, Jerusalem 91905, Israel.

出版信息

Compr Psychiatry. 2015 Apr;58:189-97. doi: 10.1016/j.comppsych.2014.12.005. Epub 2014 Dec 30.

Abstract

OBJECTIVE

Prader-Willi syndrome (PWS) is a genetic multisystem disorder with various medical, cognitive, behavioral and psychiatric problems. PWS is caused by the lack of expression of paternal genes on chromosome 15q2-q13 due to a deletion (70-75%), uniparental disomy (25-30%) or imprinting center defect (<5%). The common PWS behavioral and psychiatric characteristics are very typical in all ethnicities and were reported worldwide. Still, each individual has a specific profile of these common traits and the severity of his or her symptoms varies over time. Behavioral problems are the most important factor affecting the quality of life of both the individuals and their families. There is a need for a standardized tool to assess the specific behavioral profile of each individual and its present severity, in order to enable physicians to tailor the specific treatment needed and assist in a more accurate clinical follow up. To the best of our knowledge no such a tool has been standardized and published. We developed, based on the literature (mainly Forster and Gourash's paradigm) and our clinical experience, a 37 item disease specific questionnaire, the "PWS Behavioral Questionnaire" (PWSBQ) for assessing behavior in PWS patients. The purpose of the present study was to validate this tool in the entire adolescent and adult PWS population in Israel.

METHODS

The PWSBQ focuses on five major domains-abnormal emotional regulation, food-seeking related behavior, lack of flexibility, oppositional behavior and interpersonal problems and lastly body related behaviors. Caregivers of all Hebrew speaking individuals with PWS over the age of 12 years attending the Israeli national multidisciplinary PWS clinic were recruited. Of the 54 eligible individuals, 53 participated. They were interviewed with the PWSBQ and in addition filled the "Hyperphagia Questionnaire" and the "Child Behavioral Checklist" (CBCL). After verifying the questionnaire's content validity, all items on the PWSBQ were analyzed for internal reliability by calculating Cronbach's α. Criterion validity was evaluated by correlation testing with regard to the Hyperphagia Questionnaire and CBCL. In order to assess the questionnaire's interpretability, the correlation between the PWSBQ and the "Clinical Global Impression" (CGI) scores was evaluated.

RESULTS

The PWSBQ total score was positively correlated with both the CBCL total score and the CGI score (0.662 and 0.549, p<0.001 respectively). Of the five domains, four had acceptable internal reliability (excluding the body related behaviors domain, which was thus removed from the total score). Criterion validity was established for the four domains remaining in the statistical analysis (abnormal emotional regulation, food seeking related behavior, lack of flexibility and oppositional behavior and interpersonal problems).

CONCLUSIONS

Our findings suggest that the PWSBQ is a valid and reliable tool for the assessment of current behavioral problems among individuals with PWS. Although further research is needed in order to verify PWSBQ's ability to identify changes in the behavioral status of a given individual, it can now be used both in research and in a clinical setting, enabling the physician to plan the most suitable treatment based on the current behavioral status.

摘要

目的

普拉德-威利综合征(PWS)是一种具有多种医学、认知、行为和精神问题的遗传多系统疾病。PWS 是由于染色体 15q2-q13 上父系基因表达缺失(70-75%)、单亲二倍体(25-30%)或印迹中心缺陷(<5%)引起的。常见的 PWS 行为和精神特征在所有种族中都非常典型,并在全球范围内报道过。然而,每个人都有自己特定的这些常见特征的特征,并且他或她的症状的严重程度随时间而变化。行为问题是影响个人及其家庭生活质量的最重要因素。需要一种标准化的工具来评估每个人的特定行为特征及其当前的严重程度,以便医生能够定制所需的特定治疗,并有助于更准确的临床随访。据我们所知,还没有这样的工具被标准化和发布。我们根据文献(主要是福斯特和 Gourash 的范例)和我们的临床经验,开发了一种 37 项疾病特异性问卷,即“PWS 行为问卷”(PWSBQ),用于评估 PWS 患者的行为。本研究的目的是在以色列的所有青少年和成年 PWS 人群中验证该工具。

方法

PWSBQ 主要关注五个主要领域——异常情绪调节、与食物寻求相关的行为、缺乏灵活性、对立行为和人际关系问题以及最后是与身体相关的行为。招募了所有年龄在 12 岁以上、正在参加以色列国家多学科 PWS 诊所的希伯来语 PWS 患者的照顾者。在 54 名符合条件的患者中,有 53 名患者参与了研究。他们接受了 PWSBQ 访谈,并填写了“贪食症问卷”和“儿童行为检查表”(CBCL)。在验证问卷的内容有效性后,通过计算 Cronbach's α 来分析 PWSBQ 上的所有项目的内部可靠性。通过相关性测试,用 Hyperphagia Questionnaire 和 CBCL 来评估标准有效性。为了评估问卷的可解释性,评估了 PWSBQ 与“临床总体印象”(CGI)评分之间的相关性。

结果

PWSBQ 总分与 CBCL 总分和 CGI 评分呈正相关(分别为 0.662 和 0.549,p<0.001)。在五个领域中,有四个领域具有可接受的内部可靠性(不包括与身体相关的行为领域,因此从总分中删除)。在统计分析中保留了四个领域的标准有效性(异常情绪调节、与食物寻求相关的行为、缺乏灵活性和对立行为及人际关系问题)。

结论

我们的研究结果表明,PWSBQ 是一种评估 PWS 患者当前行为问题的有效且可靠的工具。尽管还需要进一步的研究来验证 PWSBQ 识别个体行为状态变化的能力,但它现在可以在研究和临床环境中使用,使医生能够根据当前的行为状态制定最合适的治疗方案。

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