Alteration of the circadian clock in children with Smith-Magenis syndrome
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
22162479
DOI
10.1210/jc.2011-2750
PII: jc.2011-2750
Knihovny.cz E-zdroje
- MeSH
- cirkadiánní hodiny genetika fyziologie MeSH
- cirkadiánní rytmus genetika MeSH
- dítě MeSH
- lidé MeSH
- melatonin analýza metabolismus MeSH
- mladiství MeSH
- předškolní dítě MeSH
- proteiny CLOCK genetika metabolismus MeSH
- sliny chemie metabolismus MeSH
- Smithův-Magenisův syndrom genetika metabolismus patofyziologie MeSH
- stanovení celkové genové exprese MeSH
- studie případů a kontrol MeSH
- Check Tag
- dítě MeSH
- lidé MeSH
- mladiství MeSH
- mužské pohlaví MeSH
- předškolní dítě MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- melatonin MeSH
- proteiny CLOCK MeSH
CONTEXT: Smith-Magenis syndrome (SMS) is associated with sleep disturbances and disrupted melatonin production. OBJECTIVES: The study aimed to ascertain whether the sleep and melatonin production anomalies in SMS patients may be due to an alteration of the molecular mechanism of the circadian clock. SUBJECTS AND METHODS: Five SMS patients (3-17 yr old) and five healthy age-matched control subjects were involved in the study. Saliva and buccal scrub samples were collected every 4 h during a 24-h period. Daily profiles of melatonin were determined in saliva using a direct double-antibody radioimmunoassay. Daily profiles of clock gene mRNA levels (Per1, Per2, and Rev-erbα) were determined in buccal scrub samples by RT-PCR. RESULTS: In controls, melatonin levels were elevated during the nighttime and very low during the daytime. Daily profiles of clock genes, Per1, Per2, and Rev-erbα, mRNA levels in buccal mucosa exhibited significant and mutually synchronized circadian variations (Per1 and Rev-erbα: P < 0.001; Per2: P < 0.05); the mRNA levels were elevated during the daytime and decreased during the nighttime. In SMS patients, melatonin profiles were significantly altered compared with controls, being phase reversed, phase advanced, depressed, or abolished. Only Per1 and Rev-erbα mRNA profiles exhibited significant circadian rhythms (P < 0.05); the Per2 expression exhibited high variability, and the profile was out of phase with the other clock genes. CONCLUSION: Our findings suggest that the anomalies in melatonin profiles of SMS patients might be due to a disturbance of the molecular circadian clockwork.
Citace poskytuje Crossref.org