Sleep Apnea, Obstructive Clinical Trial
Official title:
The Changes of Patterns of Microarray in Patients With Obstructive Sleep Apnea
The aim of this study are (1) To genome-wide profile the gene expression patterns of peripheral blood mononuclear cell (PBMC) in patients with obstructive sleep apnea (OSA) (2) To profile the gene expression patterns change before and after treatment with continuous positive airway pressure (CPAP) (3) To correlate the altered gene expression with the severity of the disease and outcome of OSA patients
Obstructive sleep apnea syndrome (OSAS) is characterized with recurrent collapse of upper
airway during sleep and resulted in hypoxia and sleep fragmentation. Several systemic and
cardiovascular complications have been attributed to OSAS, which is caused by hypoxia and
bursts of sympathetic activity. Increase of inflammatory mediators, which included
C-reactive protein, oxidative stress, adhesion molecules, vascular endothelial growth factor
and proinflammatory cytokines, were thought to involve in the developments of cardiovascular
diseases in patients with OSAS. In our preliminary study, both serum levels of IL-6 and CRP
were higher in patients with OSAS than control subjects, and the levels were inversely
correlated with the lowest pulse oxygen saturation. Factors triggering inflammatory cascades
in OSAS included hypoxia and sympathetic hyperactivity.
Hypoxia was thought to be the trigger factor for the elevated production of inflammatory
mediators. Through the induction of transcriptional factors and critical signaling pathways,
hypoxia induces several physiologic responses, like increased anaerobic metabolism,
angiogenesis, vasodilation, erythropoiesis and increased breathing.
Microarray is the more mature gene analysis techniques so far, which can allow high
throughput analysis of the function of many genes. Microarray can be used to understand the
disease mechanisms and is also very useful to improve disease diagnosis, disease
classification, prognosis evaluation and to improve treatment outcome. In this project, we
use oligo microarray to genome-wide profile the altered gene expressions in peripheral blood
mononuclear cells of OSAS patients; and to correlate the dysregulations of gene expression
with the clinical outcome. We will also examine the gene expression patterns change before
and after treatment with CPAP. The information obtained by this approach will be very useful
to understand the pathogenic mechanism of OSAS that leads to the systemic and cardiovascular
complications. Further therapeutic intervention may therefore be possible.
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Allocation: Non-Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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