Dominic Gilliand, Tsogyal D Latshang, Sayaka S Aeschbacher, Fabienne Huber, Deborah Flueck, Mona Lichtblau, Stefanie Ulrich, Elisabeth D Hasler, Philipp M Scheiwiller, Julian Müller, Silvia Ulrich, Konrad E Bloch, Michael Furian
{"title":"中等海拔和夜间氧疗对COPD患者脑血管功能的影响:一项2048米的随机交叉试验。","authors":"Dominic Gilliand, Tsogyal D Latshang, Sayaka S Aeschbacher, Fabienne Huber, Deborah Flueck, Mona Lichtblau, Stefanie Ulrich, Elisabeth D Hasler, Philipp M Scheiwiller, Julian Müller, Silvia Ulrich, Konrad E Bloch, Michael Furian","doi":"10.1113/EP093003","DOIUrl":null,"url":null,"abstract":"<p><p>We investigated whether nocturnal oxygen therapy improves next-day cerebrovascular function in lowlanders with chronic obstructive pulmonary disease (COPD) staying at moderate altitude. This randomized, placebo-controlled single-blind crossover trial was performed in moderate-to-severe COPD patients [forced expiratory volume in 1 s (FEV<sub>1</sub>)/forced vital capacity (FVC) <0.7; FEV<sub>1</sub> 30%-80% of predicted], living at <800 m a.s.l. and arterial oxygen saturation ( <math> <semantics><msub><mi>S</mi> <mrow><mi>p</mi> <msub><mi>O</mi> <mn>2</mn></msub> </mrow> </msub> <annotation>${{S}_{{\\mathrm{p}}{{{\\mathrm{O}}}_2}}}$</annotation></semantics> </math> ) measured with pulse oximetry ≥92%. Patients underwent assessments at 490 m and during two separate sojourns of 2 days at 2048 m, receiving either 3 L min<sup>-1</sup> nocturnal oxygen therapy or placebo in a randomized crossover design. At both altitudes, <math> <semantics><msub><mi>S</mi> <mrow><mi>p</mi> <msub><mi>O</mi> <mn>2</mn></msub> </mrow> </msub> <annotation>${{S}_{{\\mathrm{p}}{{{\\mathrm{O}}}_2}}}$</annotation></semantics> </math> , cerebral tissue oxygenation (CTO, measured by near-infrared spectroscopy), mean arterial blood pressure (MAP, measured by finger plethysmography) and middle cerebral artery systolic peak blood flow velocity (sMCAv, measured by transcranial Doppler ultrasound) were assessed while patients were quietly breathing with fraction of inspired O<sub>2</sub> ( <math> <semantics><msub><mi>F</mi> <mrow><mi>I</mi> <msub><mi>O</mi> <mn>2</mn></msub> </mrow> </msub> <annotation>${{F}_{{\\mathrm{I}}{{{\\mathrm{O}}}_2}}}$</annotation></semantics> </math> ) 0.21, with <math> <semantics><msub><mi>F</mi> <mrow><mi>I</mi> <msub><mi>O</mi> <mn>2</mn></msub> </mrow> </msub> <annotation>${{F}_{{\\mathrm{I}}{{{\\mathrm{O}}}_2}}}$</annotation></semantics> </math> 1.0, voluntarily hyperventilating, voluntarily hyperventilating with <math> <semantics><msub><mi>F</mi> <mrow><mi>I</mi> <msub><mi>O</mi> <mn>2</mn></msub> </mrow> </msub> <annotation>${{F}_{{\\mathrm{I}}{{{\\mathrm{O}}}_2}}}$</annotation></semantics> </math> 1.0, and during a head-up tilt. Overall, 18 patients (8 women) aged (mean ± SD) 65 ± 5 years, with FEV<sub>1</sub> 54.7% ± 13.9% predicted were analysed. At 2048 m under <math> <semantics><msub><mi>F</mi> <msub><mi>IO</mi> <mn>2</mn></msub> </msub> <annotation>${F}_{{\\mathrm{IO}}_{2}}$</annotation></semantics> </math> 0.21, patients became hypoxaemic ( <math> <semantics><msub><mi>S</mi> <mrow><mi>p</mi> <msub><mi>O</mi> <mn>2</mn></msub> </mrow> </msub> <annotation>${{S}_{{\\mathrm{p}}{{{\\mathrm{O}}}_2}}}$</annotation></semantics> </math> 90.3% ± 1.6%), while MAP, CTO and sMCAv remained unchanged compared with 490 m. All ventilatory manoeuvres at 2048 m induced greater increases in <math> <semantics><msub><mi>S</mi> <mrow><mi>p</mi> <msub><mi>O</mi> <mn>2</mn></msub> </mrow> </msub> <annotation>${{S}_{{\\mathrm{p}}{{{\\mathrm{O}}}_2}}}$</annotation></semantics> </math> compared with 490 m, while changes in MAP, CTO and sMCAv were similar. Head-up tilt induced a similar decrease in blood pressure, whereas sMCAv changed less in response to systemic hypotension (ΔsMCAv/ΔMAP 0.9 ± 1.3 vs. 2.3 ± 1.7 cm s<sup>-1</sup> mmHg<sup>-1</sup>) at 2048 m. No effect of nocturnal oxygen therapy was observed during any manoeuvres. This randomized clinical trial in moderate-to-severe COPD patients ascending to 2048 m showed that moderate hypoxaemia does not translate to daytime cerebral hypoxia or cerebrovascular autoregulatory impairments while at rest or during ventilatory or orthostatic challenges.</p>","PeriodicalId":12092,"journal":{"name":"Experimental Physiology","volume":" ","pages":""},"PeriodicalIF":2.8000,"publicationDate":"2025-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Effect of moderate altitude and nocturnal oxygen therapy on cerebrovascular function in patients with COPD: A randomized, crossover trial at 2048 m.\",\"authors\":\"Dominic Gilliand, Tsogyal D Latshang, Sayaka S Aeschbacher, Fabienne Huber, Deborah Flueck, Mona Lichtblau, Stefanie Ulrich, Elisabeth D Hasler, Philipp M Scheiwiller, Julian Müller, Silvia Ulrich, Konrad E Bloch, Michael Furian\",\"doi\":\"10.1113/EP093003\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>We investigated whether nocturnal oxygen therapy improves next-day cerebrovascular function in lowlanders with chronic obstructive pulmonary disease (COPD) staying at moderate altitude. 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At both altitudes, <math> <semantics><msub><mi>S</mi> <mrow><mi>p</mi> <msub><mi>O</mi> <mn>2</mn></msub> </mrow> </msub> <annotation>${{S}_{{\\\\mathrm{p}}{{{\\\\mathrm{O}}}_2}}}$</annotation></semantics> </math> , cerebral tissue oxygenation (CTO, measured by near-infrared spectroscopy), mean arterial blood pressure (MAP, measured by finger plethysmography) and middle cerebral artery systolic peak blood flow velocity (sMCAv, measured by transcranial Doppler ultrasound) were assessed while patients were quietly breathing with fraction of inspired O<sub>2</sub> ( <math> <semantics><msub><mi>F</mi> <mrow><mi>I</mi> <msub><mi>O</mi> <mn>2</mn></msub> </mrow> </msub> <annotation>${{F}_{{\\\\mathrm{I}}{{{\\\\mathrm{O}}}_2}}}$</annotation></semantics> </math> ) 0.21, with <math> <semantics><msub><mi>F</mi> <mrow><mi>I</mi> <msub><mi>O</mi> <mn>2</mn></msub> </mrow> </msub> <annotation>${{F}_{{\\\\mathrm{I}}{{{\\\\mathrm{O}}}_2}}}$</annotation></semantics> </math> 1.0, voluntarily hyperventilating, voluntarily hyperventilating with <math> <semantics><msub><mi>F</mi> <mrow><mi>I</mi> <msub><mi>O</mi> <mn>2</mn></msub> </mrow> </msub> <annotation>${{F}_{{\\\\mathrm{I}}{{{\\\\mathrm{O}}}_2}}}$</annotation></semantics> </math> 1.0, and during a head-up tilt. 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引用次数: 0
摘要
我们研究了夜间氧疗是否能改善居住在中等海拔地区的低海拔地区慢性阻塞性肺疾病(COPD)患者第二天的脑血管功能。这项随机、安慰剂对照的单盲交叉试验在中重度COPD患者中进行[1秒用力呼气量(FEV1)/用力肺活量(FVC) 1为预测值的30%-80%],生活在sp2 ${{s}_{{\mathrm{p}}}{{\mathrm{O}}}_2}}}$),脉搏血氧饱和度≥92%。在随机交叉设计中,患者在海拔490米和海拔2048米的两次单独停留期间接受2天的评估,接受3l min-1夜间氧气治疗或安慰剂。在两个海拔高度,当患者安静呼吸,吸入氧气分数(F I O2 ${{F}_{{\ mathm {p}}{{\ mathm {O}}}_2}}}$) 0.21时,评估S p O2 ${{S}_{{\ mathm {p}}}{{\ mathm {O}}}}}$、脑组织氧合(CTO,近红外光谱测量)、平均动脉血压(MAP,手指体积描记仪测量)和大脑中动脉收缩峰值血流速度(sMCAv,经颅多普勒超声测量)。F I O 2 ${{F}_{{\mathrm{I}}}{{\mathrm{O}}}_2}}}$ 1.0,自动换气,F I O 2 ${{F}_{{\mathrm{I}}{{\mathrm{O}} _2}}}$ 1.0时自动换气。总体分析18例患者(8例女性),年龄(mean±SD) 65±5岁,预测FEV1 54.7%±13.9%。2048 m时,fo2 ${F}_{{\mathrm{IO}}_{2}}$ 0.21,患者出现低氧血症(so2 ${{S}_{{\mathrm{p}}{{\mathrm{O}}}_2}} $ 90.3%±1.6%),而MAP、CTO和sMCAv与4.9 m时相比没有变化。与490 m相比,2048 m各通气操作诱导的S p O 2 ${{S}_{{\mathrm{p}}{{{\mathrm{O}}}_2}}}$增加幅度较大,而MAP、CTO和sMCAv的变化相似。平头倾斜引起类似的血压下降,而sMCAv在2048 m时对全身性低血压的反应变化较小(ΔsMCAv/ΔMAP 0.9±1.3 vs. 2.3±1.7 cm s-1 mmHg-1)。在任何操作过程中均未观察到夜间氧疗的效果。这项随机临床试验对升至2048米的中重度COPD患者进行了研究,结果表明,中度低氧血症在休息或呼吸或站立时不会转化为白天脑缺氧或脑血管自身调节障碍。
Effect of moderate altitude and nocturnal oxygen therapy on cerebrovascular function in patients with COPD: A randomized, crossover trial at 2048 m.
We investigated whether nocturnal oxygen therapy improves next-day cerebrovascular function in lowlanders with chronic obstructive pulmonary disease (COPD) staying at moderate altitude. This randomized, placebo-controlled single-blind crossover trial was performed in moderate-to-severe COPD patients [forced expiratory volume in 1 s (FEV1)/forced vital capacity (FVC) <0.7; FEV1 30%-80% of predicted], living at <800 m a.s.l. and arterial oxygen saturation ( ) measured with pulse oximetry ≥92%. Patients underwent assessments at 490 m and during two separate sojourns of 2 days at 2048 m, receiving either 3 L min-1 nocturnal oxygen therapy or placebo in a randomized crossover design. At both altitudes, , cerebral tissue oxygenation (CTO, measured by near-infrared spectroscopy), mean arterial blood pressure (MAP, measured by finger plethysmography) and middle cerebral artery systolic peak blood flow velocity (sMCAv, measured by transcranial Doppler ultrasound) were assessed while patients were quietly breathing with fraction of inspired O2 ( ) 0.21, with 1.0, voluntarily hyperventilating, voluntarily hyperventilating with 1.0, and during a head-up tilt. Overall, 18 patients (8 women) aged (mean ± SD) 65 ± 5 years, with FEV1 54.7% ± 13.9% predicted were analysed. At 2048 m under 0.21, patients became hypoxaemic ( 90.3% ± 1.6%), while MAP, CTO and sMCAv remained unchanged compared with 490 m. All ventilatory manoeuvres at 2048 m induced greater increases in compared with 490 m, while changes in MAP, CTO and sMCAv were similar. Head-up tilt induced a similar decrease in blood pressure, whereas sMCAv changed less in response to systemic hypotension (ΔsMCAv/ΔMAP 0.9 ± 1.3 vs. 2.3 ± 1.7 cm s-1 mmHg-1) at 2048 m. No effect of nocturnal oxygen therapy was observed during any manoeuvres. This randomized clinical trial in moderate-to-severe COPD patients ascending to 2048 m showed that moderate hypoxaemia does not translate to daytime cerebral hypoxia or cerebrovascular autoregulatory impairments while at rest or during ventilatory or orthostatic challenges.
期刊介绍:
Experimental Physiology publishes research papers that report novel insights into homeostatic and adaptive responses in health, as well as those that further our understanding of pathophysiological mechanisms in disease. We encourage papers that embrace the journal’s orientation of translation and integration, including studies of the adaptive responses to exercise, acute and chronic environmental stressors, growth and aging, and diseases where integrative homeostatic mechanisms play a key role in the response to and evolution of the disease process. Examples of such diseases include hypertension, heart failure, hypoxic lung disease, endocrine and neurological disorders. We are also keen to publish research that has a translational aspect or clinical application. Comparative physiology work that can be applied to aid the understanding human physiology is also encouraged.
Manuscripts that report the use of bioinformatic, genomic, molecular, proteomic and cellular techniques to provide novel insights into integrative physiological and pathophysiological mechanisms are welcomed.