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Effects of obstructive sleep apnea on serum brain-derived neurotrophic factor protein, cortisol, and lipid levels

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dc.contributor.author Panaree B.
dc.contributor.author Chantana M.
dc.contributor.author Wasana S.
dc.contributor.author Chairat N.
dc.date.accessioned 2021-04-05T03:34:47Z
dc.date.available 2021-04-05T03:34:47Z
dc.date.issued 2011
dc.identifier.issn 15209512
dc.identifier.other 2-s2.0-84859389181
dc.identifier.uri https://ir.swu.ac.th/jspui/handle/123456789/14436
dc.identifier.uri https://www.scopus.com/inward/record.uri?eid=2-s2.0-84859389181&doi=10.1007%2fs11325-010-0415-7&partnerID=40&md5=9d13f655ad60fc7ff6911f776adb8285
dc.description.abstract Objectives: Obstructive sleep apnea (OSA) is a sleep-disordered breathing leading to vascular endothelial cells dysfunction, cognitive impairment, and abnormal lipid metabolism. serum brain-derived neurotrophic factor (BDNF) protein, cortisol, and lipid levels in OSA were investigated. Materials and methods: All middle-aged subjects including healthy individuals without signs and symptoms of apneahypopnea and ear nose throat (ENT) outpatients were randomly recruited and screened by overnight polysomnogram (PSG). Apnea-hypopnea index (AHI) was used as a criteria to determine subjects to enroll in this program. According to AHI, they were separated into control and OSA groups. A group of 39 OSA patients (AHI≥10 events/h) and 24 control subjects (AHI<5 events/h) were selected. Serum BDNF protein was analyzed by enzyme-linked immunosorbent assay (ELISA) from venous blood collection at 8:00 a.m. following PSG. Serum cortisol was assayed by enzyme-chemiluminescense immuno assay (ECLIA). Serum lipid profile levels were determined by enzymatic colorimetric and homogeneous method. Results: Characteristics of OSA patients and control groups including gender, age, AHI, body weight, height, and BMI showed significant differences. Serum BDNF protein, cortisol, triglyceride, and total cholesterol levels in OSA and control groups were not significantly different. High density lipoprotein-cholesterol (HDL-c) in OSA was significantly lower than that of control (p=0.008) while low density lipoprotein-cholesterol (LDL-c) was significantly higher than that of control (p=0.04). Conclusions: OSA had no significant effect on serum BDNF, cortisol, triglyceride, or total cholesterol levels while LDL-c and HDL-c levels in OSA patients compared to control were significantly different at p=0.04, and p= 0.008, respectively. © Springer-Verlag 2010.
dc.subject brain derived neurotrophic factor
dc.subject cholesterol
dc.subject high density lipoprotein cholesterol
dc.subject hydrocortisone
dc.subject low density lipoprotein cholesterol
dc.subject triacylglycerol
dc.subject brain derived neurotrophic factor
dc.subject hydrocortisone
dc.subject lipid
dc.subject adult
dc.subject age
dc.subject apnea hypopnea index
dc.subject article
dc.subject body height
dc.subject body mass
dc.subject body weight
dc.subject chemoluminescence
dc.subject cholesterol blood level
dc.subject clinical article
dc.subject colorimetry
dc.subject controlled study
dc.subject enzyme linked immunosorbent assay
dc.subject female
dc.subject gender
dc.subject human
dc.subject hydrocortisone blood level
dc.subject male
dc.subject polysomnography
dc.subject priority journal
dc.subject protein blood level
dc.subject sleep apnea syndrome
dc.subject triacylglycerol blood level
dc.subject blood
dc.subject middle aged
dc.subject reference value
dc.subject sleep apnea syndrome
dc.subject Thailand
dc.subject university hospital
dc.subject Academic Medical Centers
dc.subject Adult
dc.subject Brain-Derived Neurotrophic Factor
dc.subject Female
dc.subject Humans
dc.subject Hydrocortisone
dc.subject Lipids
dc.subject Male
dc.subject Middle Aged
dc.subject Polysomnography
dc.subject Reference Values
dc.subject Sleep Apnea, Obstructive
dc.subject Thailand
dc.title Effects of obstructive sleep apnea on serum brain-derived neurotrophic factor protein, cortisol, and lipid levels
dc.type Article
dc.rights.holder Scopus
dc.identifier.bibliograpycitation Sleep and Breathing. Vol 15, No.4 (2011), p.649-656
dc.identifier.doi 10.1007/s11325-010-0415-7


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