Matches in SemOpenAlex for { <https://semopenalex.org/work/W2885505372> ?p ?o ?g. }
- W2885505372 endingPage "1903" @default.
- W2885505372 startingPage "1898" @default.
- W2885505372 abstract "Obstructive sleep apnea syndrome (OSAS) is prevalent in obesity and is associated with many metabolic abnormalities. The relationship between OSAS and bone metabolism is still unclear. The aim of this study was to investigate the relationship between the severity of OSAS and bone metabolic markers.A total of 119 obese males were enrolled in this study in spring months from 2015 to 2017. All candidates underwent polysomnography, and their bone mineral density (BMD) and the serum levels of total procollagen type 1 N-terminal propeptide (t-P1NP), N-terminal midfragment of osteocalcin (N-MID), β-C-terminal telopeptide of type 1 collagen (β-CTX), vitamin D (VD), and parathyroid hormone (PTH) were measured. The analysis of variance and Pearson correlation analysis were performed for data analyses.No significant differences in the mean values of BMD were observed among the obesity, mild-to-moderate OSAS, and severe OSAS groups; and the serum levels of t-P1NP and β-CTX in the severe OSAS group were significantly higher than those in the obesity group (48.42 ± 23.78 ng/ml vs. 31.98 ± 9.85 ng/ml, P < 0.001; 0.53 ± 0.24 ng/ml vs. 0.41 ± 0.13 ng/ml, P = 0.011, respectively). The serum level of VD in the obesity group was significantly higher than those in the mild-to-moderate and severe OSAS groups (both P < 0.001), and decreased as the severity of OSAS increased (P < 0.001). The serum level of PTH in the severe OSAS group was significantly higher than those in the obesity and mild-to-moderate OSAS groups (both P < 0.001). The results of correlation analysis indicated that the level of apnea-hypopnea index (AHI) was correlated with the levels of t-P1NP (r = 0.396, P < 0.001), VD (r = -0.404, P < 0.001), and PTH (r = 0.400, P < 0.001), whereas the level of minimum O2saturation (SaO2min) was correlated with the levels of VD (r = 0.258, P = 0.016) and PTH (r = -0.376, P < 0.001).The levels of bone resorption and formation markers in patients with severe OSAS were significantly increased compared to obese men, and the severity of OSAS was correlated with the serum levels of t-P1NP, VD, and PTH.阻塞性睡眠呼吸暂停综合征患者骨代谢标志物的研究摘要背景:阻塞性睡眠呼吸暂停综合征(obstructive sleep apnea syndrome,OSAS)多见于肥胖人群,且与多种代谢性疾病相关,而OSAS与骨代谢的关系至今仍未明确。此研究旨在探讨OSAS严重程度与骨代谢标志物的关系。 方法:纳入了2015年至2017年春季来诊的119名肥胖男性。所有参与者行多导睡眠监测,并测量骨密度(bone mineral density,BMD)及血清总I型胶原氨基端延长肽(total procollagen type1 N-terminal propeptide,t-P1NP)、N-端骨钙素(N-terminal midfragment of osteocalcin, N-MID)、β-胶原特殊序列(β-C-terminal telopeptide of type 1 collagen,β-CTX)、维生素D(vitamin D,VD)和甲状旁腺激素(parathyroid hormone,PTH)的水平。数据分析采用方差分析及Pearson相关分析。 结果:肥胖对照组、轻中度OSAS及重度OSAS组患者的BMD水平无明显差异,而重度OSAS组血清t-P1NP 和β-CTX的水平均明显高于肥胖对照组 (48.42±23.78 ng/ml vs. 31.98±9.85 ng/ml, P<0.001; 0.53±0.24 ng/ml vs. 0.41±0.13 ng/ml, P =0.011)。肥胖组的VD水平明显高于轻中度OSAS组 (P <0.001)和重度OSAS组 (P <0.001),且重度OSAS组的VD水平低于轻中度OSAS组 (P <0.001)。重度OSAS组的PTH水平明显高于轻中度OSAS组(P <0.001)及肥胖组 (P <0.001)。相关性分析显示睡眠呼吸暂停低通气指数(apnea-hypopnea index,AHI)与t-P1NP(r=0.396, P <0.001)、VD(r=-0.404, P <0.001)、PTH(r=0.400, p<0.001)相关,夜间最低血氧(minimum O2 saturation,SaO2min)与VD(r=0.258, P =0.016)和PTH(r=-0.376, P <0.001)相关。 结论:与男性肥胖人群相比,男性重度OSAS患者的骨吸收及骨形成标志物明显升高,OSAS的严重程度与血清t-P1NP、VD及PTH相关。." @default.
- W2885505372 created "2018-08-22" @default.
- W2885505372 creator A5006281138 @default.
- W2885505372 creator A5018289057 @default.
- W2885505372 creator A5020383361 @default.
- W2885505372 creator A5022559283 @default.
- W2885505372 creator A5023811522 @default.
- W2885505372 creator A5046881768 @default.
- W2885505372 creator A5047113122 @default.
- W2885505372 creator A5048114554 @default.
- W2885505372 creator A5080203880 @default.
- W2885505372 creator A5080687802 @default.
- W2885505372 creator A5083198737 @default.
- W2885505372 date "2018-08-20" @default.
- W2885505372 modified "2023-10-18" @default.
- W2885505372 title "Bone Metabolic Markers in Patients with Obstructive Sleep Apnea Syndrome" @default.
- W2885505372 cites W1541553734 @default.
- W2885505372 cites W1575863108 @default.
- W2885505372 cites W1665096084 @default.
- W2885505372 cites W1680443751 @default.
- W2885505372 cites W1967644150 @default.
- W2885505372 cites W1969810899 @default.
- W2885505372 cites W1986228197 @default.
- W2885505372 cites W1987402722 @default.
- W2885505372 cites W1988319077 @default.
- W2885505372 cites W2001568728 @default.
- W2885505372 cites W2005779589 @default.
- W2885505372 cites W2020339197 @default.
- W2885505372 cites W2023260075 @default.
- W2885505372 cites W2040626814 @default.
- W2885505372 cites W2050947989 @default.
- W2885505372 cites W2057804864 @default.
- W2885505372 cites W2063838515 @default.
- W2885505372 cites W2074816630 @default.
- W2885505372 cites W2082656849 @default.
- W2885505372 cites W2082882308 @default.
- W2885505372 cites W2088700309 @default.
- W2885505372 cites W2090442726 @default.
- W2885505372 cites W2092309785 @default.
- W2885505372 cites W2104616939 @default.
- W2885505372 cites W2104719134 @default.
- W2885505372 cites W2115635469 @default.
- W2885505372 cites W2118601027 @default.
- W2885505372 cites W2130586404 @default.
- W2885505372 cites W2132572939 @default.
- W2885505372 cites W2147576297 @default.
- W2885505372 cites W2169038550 @default.
- W2885505372 cites W2171162083 @default.
- W2885505372 cites W2517652672 @default.
- W2885505372 cites W2538033908 @default.
- W2885505372 cites W2560774896 @default.
- W2885505372 cites W2602106803 @default.
- W2885505372 doi "https://doi.org/10.4103/0366-6999.238149" @default.
- W2885505372 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6085856" @default.
- W2885505372 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30082519" @default.
- W2885505372 hasPublicationYear "2018" @default.
- W2885505372 type Work @default.
- W2885505372 sameAs 2885505372 @default.
- W2885505372 citedByCount "11" @default.
- W2885505372 countsByYear W28855053722018 @default.
- W2885505372 countsByYear W28855053722019 @default.
- W2885505372 countsByYear W28855053722020 @default.
- W2885505372 countsByYear W28855053722021 @default.
- W2885505372 countsByYear W28855053722022 @default.
- W2885505372 countsByYear W28855053722023 @default.
- W2885505372 crossrefType "journal-article" @default.
- W2885505372 hasAuthorship W2885505372A5006281138 @default.
- W2885505372 hasAuthorship W2885505372A5018289057 @default.
- W2885505372 hasAuthorship W2885505372A5020383361 @default.
- W2885505372 hasAuthorship W2885505372A5022559283 @default.
- W2885505372 hasAuthorship W2885505372A5023811522 @default.
- W2885505372 hasAuthorship W2885505372A5046881768 @default.
- W2885505372 hasAuthorship W2885505372A5047113122 @default.
- W2885505372 hasAuthorship W2885505372A5048114554 @default.
- W2885505372 hasAuthorship W2885505372A5080203880 @default.
- W2885505372 hasAuthorship W2885505372A5080687802 @default.
- W2885505372 hasAuthorship W2885505372A5083198737 @default.
- W2885505372 hasBestOaLocation W28855053721 @default.
- W2885505372 hasConcept C124490489 @default.
- W2885505372 hasConcept C125870589 @default.
- W2885505372 hasConcept C126322002 @default.
- W2885505372 hasConcept C131075544 @default.
- W2885505372 hasConcept C134018914 @default.
- W2885505372 hasConcept C160160445 @default.
- W2885505372 hasConcept C170033053 @default.
- W2885505372 hasConcept C181199279 @default.
- W2885505372 hasConcept C2776006263 @default.
- W2885505372 hasConcept C2776541429 @default.
- W2885505372 hasConcept C2776886416 @default.
- W2885505372 hasConcept C2777935920 @default.
- W2885505372 hasConcept C2778205975 @default.
- W2885505372 hasConcept C2781208988 @default.
- W2885505372 hasConcept C2781326671 @default.
- W2885505372 hasConcept C511355011 @default.
- W2885505372 hasConcept C519063684 @default.
- W2885505372 hasConcept C55493867 @default.
- W2885505372 hasConcept C64348721 @default.
- W2885505372 hasConcept C71924100 @default.