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青少年不宁腿综合征/ Willis-Ekbom 病的患病率、其临床特征及其对日常功能的影响。

The prevalence of the restless legs Syndrome/Willis-Ekbom disease among teenagers, its clinical characteristics and impact on everyday functioning.

机构信息

Developmental Neurology Department, Chair of Neurology, Medical University of Gdańsk, Poland.

Department of Neurosurgery, University Clinical Center in Gdańsk, Poland.

出版信息

Sleep Med. 2022 Jan;89:48-54. doi: 10.1016/j.sleep.2021.10.004. Epub 2021 Oct 28.

Abstract

BACKGROUND AND AIMS

The data on the prevalence of the Restless Legs Syndrome/Willis -Ekbom disease (RLS/WED) in the population of teenagers is scarce. The aim of this study was to determine RLS/WED occurrence in adolescents, its diagnostic accuracy, family history, clinical characteristics and impact on everyday functioning.

MATERIAL AND METHODS

A group of 2379 pupils (aged 13-18 y.o.) from 6 randomly selected secondary schools in Gdańsk, Poland were screened for RLS/WED with the use of a questionnaire. In order to verify the diagnosis and perform additional tests (neurological examination, psychological evaluation, biochemical blood tests, demographic questionnaire, International RLS rating scale/IRLSS, Epworth daytime sleepiness scale). all of the respondents with RLS/WED suspicion and their parents were asked for a consultation by a child neurologist. Both children and parents with RLS/WED diagnosis were tested with actigraphy at home for at least two consecutive nights.

RESULTS

Two thousand and ninety seven students (88,15%) filled the questionnaire correctly (1171 girls and 926 boys, 56% and 44%). Sixty four respondents were suspected of having RLS/WED (3,1%), however, 36 of them were diagnosed as RLS/WED-mimics (mainly positional discomfort). Finally, 21 (1%) were diagnosed with definite idiopathic RLS/WED. The average age of symptom onset was 10.96 years. The severity was moderate in the most of the cases (61.9%) and the course of the disease was intermittent in all of them. Family history was positive in 80%. Abnormal actigraphy (PLMS index >5/h) was present in 80%. Blood level of ferritin was low (<50 ng/ml) in 85%. Excessive daytime sleepiness and school problems affected almost half of them. The presence of RLS/WED symptoms was associated with disrupted sleep, behavioral problems (irritability, aggression, hyperactivity), attention deficit and lowered mood. No correlation between RLS/WED and attention deficit hyperactivity disorder (ADHD), nocturnal enuresis or primary headaches was found. Thirty eight percent of the patients sought medical help, but none of them obtained proper diagnosis nor treatment of RLS/WED.

CONCLUSIONS

In this study restless legs syndrome affected 1% of Polish teenagers, in the majority of cases was idiopathic and associated with positive family history. It affected sleep and everyday functioning. Neurological consultation is essential to avoid false positive diagnoses of RLS/WED in teenagers.

摘要

背景和目的

关于青少年人群中不宁腿综合征/ Willis-Ekbom 病(RLS/WED)患病率的数据很少。本研究旨在确定青少年 RLS/WED 的发生情况、其诊断准确性、家族史、临床特征及其对日常功能的影响。

材料和方法

研究组包括 2379 名来自波兰格但斯克市 6 所随机抽取的中学的学生(年龄 13-18 岁),他们使用问卷筛查 RLS/WED。为了验证诊断并进行额外的检查(神经系统检查、心理评估、生化血液检查、人口学问卷、国际 RLS 评分量表/IRLSS、Epworth 白天嗜睡量表),所有怀疑患有 RLS/WED 的患者及其父母都被邀请由儿童神经病学家进行会诊。所有被诊断为 RLS/WED 的儿童及其父母都在家中使用活动记录仪进行至少两个连续晚上的测试。

结果

2097 名学生(88.15%)正确填写了问卷(1171 名女生和 926 名男生,分别占 56%和 44%)。有 64 名学生被怀疑患有 RLS/WED(3.1%),但其中 36 名被诊断为 RLS/WED 样症状(主要为体位不适)。最终,21 名(1%)被诊断为明确的特发性 RLS/WED。症状出现的平均年龄为 10.96 岁。大多数患者的病情严重程度为中度(61.9%),所有患者的病情均为间歇性。家族史阳性率为 80%。80%的患者存在异常的活动记录仪(PLMS 指数>5/h)。85%的患者血铁蛋白水平较低(<50ng/ml)。几乎一半的患者出现白天嗜睡和学业问题。存在 RLS/WED 症状与睡眠中断、行为问题(易怒、攻击性、多动)、注意力缺陷和情绪低落有关。未发现 RLS/WED 与注意缺陷多动障碍(ADHD)、夜间遗尿或原发性头痛之间存在相关性。38%的患者寻求医疗帮助,但他们都没有得到 RLS/WED 的正确诊断和治疗。

结论

在这项研究中,不宁腿综合征影响了 1%的波兰青少年,大多数情况下为特发性且与阳性家族史相关。它影响睡眠和日常功能。神经科会诊对于避免青少年 RLS/WED 的假阳性诊断至关重要。

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