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本文引用的文献

1
Review of disrupted sleep patterns in Smith-Magenis syndrome and normal melatonin secretion in a patient with an atypical interstitial 17p11.2 deletion.对一名患有非典型17号染色体短臂11.2区间质缺失的患者的睡眠模式紊乱及正常褪黑素分泌情况的综述。
Am J Med Genet A. 2009 Jul;149A(7):1382-91. doi: 10.1002/ajmg.a.32846.
2
Melatonin and human chronobiology.褪黑素与人类生物钟学
Cold Spring Harb Symp Quant Biol. 2007;72:623-36. doi: 10.1101/sqb.2007.72.055.
3
Sleep and sleep disturbances: biological basis and clinical implications.睡眠与睡眠障碍:生物学基础及临床意义
Cell Mol Life Sci. 2007 May;64(10):1174-86. doi: 10.1007/s00018-007-6529-9.
4
Excretion of 6-hydroxymelatonin sulfate (6-OHMS) in siblings during childhood and adolescence.儿童期和青春期兄弟姐妹中硫酸6-羟基褪黑素(6-OHMS)的排泄情况。
Neuroendocrinology. 2003 Nov;78(5):241-3. doi: 10.1159/000074444.
5
Point and interval estimations of circadian melatonin ecphasia in Smith-Magenis syndrome.史密斯-马吉尼斯综合征中昼夜节律褪黑素分泌异常的点估计和区间估计。
Biomed Pharmacother. 2003 Oct;57 Suppl 1:31s-34s. doi: 10.1016/j.biopha.2003.08.004.
6
Melatonin: clinical relevance.褪黑素:临床相关性。
Best Pract Res Clin Endocrinol Metab. 2003 Jun;17(2):273-85. doi: 10.1016/s1521-690x(03)00016-2.
7
Mutations in RAI1 associated with Smith-Magenis syndrome.与史密斯-马吉尼斯综合征相关的RAI1基因突变。
Nat Genet. 2003 Apr;33(4):466-8. doi: 10.1038/ng1126. Epub 2003 Mar 24.
8
Exercise elicits phase shifts and acute alterations of melatonin that vary with circadian phase.运动引发褪黑素的相位变化和急性改变,这些变化随昼夜节律相位而不同。
Am J Physiol Regul Integr Comp Physiol. 2003 Mar;284(3):R714-24. doi: 10.1152/ajpregu.00355.2002.
9
Melatonin treatment for age-related insomnia.褪黑素治疗与年龄相关的失眠症。
J Clin Endocrinol Metab. 2001 Oct;86(10):4727-30. doi: 10.1210/jcem.86.10.7901.
10
beta(1)-adrenergic antagonists improve sleep and behavioural disturbances in a circadian disorder, Smith-Magenis syndrome.β1-肾上腺素能拮抗剂可改善昼夜节律紊乱疾病——史密斯-马吉尼斯综合征的睡眠和行为障碍。
J Med Genet. 2001 Sep;38(9):586-90. doi: 10.1136/jmg.38.9.586.

日间唾液褪黑素水平在 Smith-Magenis 综合征中的诊断效用。

Diagnostic utility of daytime salivary melatonin levels in Smith-Magenis syndrome.

机构信息

Department of Medicine, University of Alberta, Edmonton, AB, Canada.

出版信息

Am J Med Genet A. 2010 Jan;152A(1):96-101. doi: 10.1002/ajmg.a.33158.

DOI:10.1002/ajmg.a.33158
PMID:20034098
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2802065/
Abstract

An inverted circadian rhythm of melatonin (MT) likely contributes to the sleep disturbance in patients with Smith-Magenis syndrome (SMS). Plasma MT levels have documented this altered rhythm, but daytime levels of salivary MT has not been determined. Daytime measures of salivary MT might have utility in home/outpatient settings for assessing MT levels in undiagnosed patients with clinical features of SMS. The objective of this study was to determine the utility of daytime salivary MT as a diagnostic test in SMS. Thirty individuals with confirmed SMS [28 with del 17p11.2 and 2 with the retinoic acid induced 1 (RAI1) gene mutation] and five controls were studied. Single or serial daytime salivary MT levels were measured. The mean midday salivary MT level was 79.0 pg/ml in SMS patients, compared with 16.3 pg/ml in controls, with nine patients having values similar to controls. The median MT level in SMS patients was 49.0 pg/ml (first and third quartile values = 15.5 and 106.8 pg/ml). Twenty-six (90%) of 29 patients had at least one MT value >15.5 pg/ml, including 70 (78%) of 90 samples from patients with del 17p11.2 and one (20%) of five samples from the two patients with the RAI1 mutation. Neither the pattern of medication use nor age had an effect on daytime salivary MT levels. Although most SMS patients had elevated daytime salivary MT levels, multiple sampling appears necessary to distinguish patients with SMS from other conditions.

摘要

褪黑素(MT)的昼夜节律颠倒可能导致 Smith-Magenis 综合征(SMS)患者的睡眠障碍。血浆 MT 水平已经证明了这种改变的节律,但唾液 MT 的日间水平尚未确定。唾液 MT 的日间测量可能在家庭/门诊环境中用于评估具有 SMS 临床特征但未经诊断的患者的 MT 水平有用。本研究的目的是确定日间唾液 MT 作为 SMS 诊断测试的效用。研究了 30 名确诊为 SMS 的个体[28 名携带 del 17p11.2,2 名携带维甲酸诱导 1(RAI1)基因突变]和 5 名对照者。测量了单次或连续的日间唾液 MT 水平。SMS 患者的平均中午唾液 MT 水平为 79.0pg/ml,而对照组为 16.3pg/ml,其中 9 名患者的数值与对照组相似。SMS 患者的 MT 中位数为 49.0pg/ml(第一和第三四分位数值=15.5 和 106.8pg/ml)。29 名患者中的 26 名(90%)至少有一次 MT 值>15.5pg/ml,包括 70 份(78%)来自 del 17p11.2 的患者的样本和 5 名 RAI1 基因突变患者的 1 份(20%)样本。药物使用模式或年龄均未对日间唾液 MT 水平产生影响。尽管大多数 SMS 患者的日间唾液 MT 水平升高,但需要多次采样才能将 SMS 患者与其他疾病区分开来。