Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/14436
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dc.contributor.authorPanaree B.
dc.contributor.authorChantana M.
dc.contributor.authorWasana S.
dc.contributor.authorChairat N.
dc.date.accessioned2021-04-05T03:34:47Z-
dc.date.available2021-04-05T03:34:47Z-
dc.date.issued2011
dc.identifier.issn15209512
dc.identifier.other2-s2.0-84859389181
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/14436-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84859389181&doi=10.1007%2fs11325-010-0415-7&partnerID=40&md5=9d13f655ad60fc7ff6911f776adb8285
dc.description.abstractObjectives: 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.subjectbrain derived neurotrophic factor
dc.subjectcholesterol
dc.subjecthigh density lipoprotein cholesterol
dc.subjecthydrocortisone
dc.subjectlow density lipoprotein cholesterol
dc.subjecttriacylglycerol
dc.subjectbrain derived neurotrophic factor
dc.subjecthydrocortisone
dc.subjectlipid
dc.subjectadult
dc.subjectage
dc.subjectapnea hypopnea index
dc.subjectarticle
dc.subjectbody height
dc.subjectbody mass
dc.subjectbody weight
dc.subjectchemoluminescence
dc.subjectcholesterol blood level
dc.subjectclinical article
dc.subjectcolorimetry
dc.subjectcontrolled study
dc.subjectenzyme linked immunosorbent assay
dc.subjectfemale
dc.subjectgender
dc.subjecthuman
dc.subjecthydrocortisone blood level
dc.subjectmale
dc.subjectpolysomnography
dc.subjectpriority journal
dc.subjectprotein blood level
dc.subjectsleep apnea syndrome
dc.subjecttriacylglycerol blood level
dc.subjectblood
dc.subjectmiddle aged
dc.subjectreference value
dc.subjectsleep apnea syndrome
dc.subjectThailand
dc.subjectuniversity hospital
dc.subjectAcademic Medical Centers
dc.subjectAdult
dc.subjectBrain-Derived Neurotrophic Factor
dc.subjectFemale
dc.subjectHumans
dc.subjectHydrocortisone
dc.subjectLipids
dc.subjectMale
dc.subjectMiddle Aged
dc.subjectPolysomnography
dc.subjectReference Values
dc.subjectSleep Apnea, Obstructive
dc.subjectThailand
dc.titleEffects of obstructive sleep apnea on serum brain-derived neurotrophic factor protein, cortisol, and lipid levels
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationSleep and Breathing. Vol 15, No.4 (2011), p.649-656
dc.identifier.doi10.1007/s11325-010-0415-7
Appears in Collections:Scopus 1983-2021

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