Augmented vasoreactivity in adult life associated with perinatal vascular insult
Adverse environmental events occurring early in life have received little attention as predictors of disease in the later stages of life. At birth, the transition from gas exchange by the placenta to gas exchange by the lungs requires dramatic changes in the pulmonary circulation, which during this...
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Veröffentlicht in: | The Lancet (British edition) 1999-06, Vol.353 (9171), p.2205-2207 |
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description | Adverse environmental events occurring early in life have received little attention as predictors of disease in the later stages of life. At birth, the transition from gas exchange by the placenta to gas exchange by the lungs requires dramatic changes in the pulmonary circulation, which during this period is particularly vulnerable to noxious stimuli. We measured pulmonary-artery pressure responses to high-altitude exposure, a stimulus that causes pronounced pulmonary vasoconstriction, in young adults who had had transient perinatal hypoxic pulmonary hypertension and in controls of similar age and sex distribution.
Review of neonatal-care records at the Lausanne University Hospital for Children identified 15 individuals who met the eligibility criteria (birth at 3·34 weeks of gestation, persistence of hypoxaemia during ventilation with oxygen during the first week of life, and persistence of fetal circulation). Ten of these individuals agreed to take part; the control group was ten volunteers without any history of perinatal complications. Systolic pulmonary-artery pressure (by echocardiography) and arterial oxygen saturation were measured at baseline and at high altitude (4559 m).
The mean increase in pulmonary-artery pressure at high altitude was significantly greater (p=0·01) in the participants who had had perinatal pulmonary hypertension (from 26·2 mm Hg [SD 2·1] to 62·3 mm Hg [7·3]) than in the controls (from 25·8 mm Hg [2·3] to 49·7 mm Hg [11·3]). The fall in arterial oxygen saturation was similar in the two groups.
These findings suggest that a transient perinatal insult to the pulmonary circulation leaves a persistent and potentially fatal imprint, which when activated in adult life predisposes to a pathological response. Survivors of perinatal pulmonary hypertension may be at risk of developing this disorder in later life. |
doi_str_mv | 10.1016/S0140-6736(98)08352-4 |
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Review of neonatal-care records at the Lausanne University Hospital for Children identified 15 individuals who met the eligibility criteria (birth at 3·34 weeks of gestation, persistence of hypoxaemia during ventilation with oxygen during the first week of life, and persistence of fetal circulation). Ten of these individuals agreed to take part; the control group was ten volunteers without any history of perinatal complications. Systolic pulmonary-artery pressure (by echocardiography) and arterial oxygen saturation were measured at baseline and at high altitude (4559 m).
The mean increase in pulmonary-artery pressure at high altitude was significantly greater (p=0·01) in the participants who had had perinatal pulmonary hypertension (from 26·2 mm Hg [SD 2·1] to 62·3 mm Hg [7·3]) than in the controls (from 25·8 mm Hg [2·3] to 49·7 mm Hg [11·3]). The fall in arterial oxygen saturation was similar in the two groups.
These findings suggest that a transient perinatal insult to the pulmonary circulation leaves a persistent and potentially fatal imprint, which when activated in adult life predisposes to a pathological response. Survivors of perinatal pulmonary hypertension may be at risk of developing this disorder in later life.</description><identifier>ISSN: 0140-6736</identifier><identifier>EISSN: 1474-547X</identifier><identifier>DOI: 10.1016/S0140-6736(98)08352-4</identifier><identifier>PMID: 10392986</identifier><identifier>CODEN: LANCAO</identifier><language>eng</language><publisher>London: Elsevier Ltd</publisher><subject>Adult ; Adults ; Age composition ; Altitude ; Atmospheric pressure ; Biological and medical sciences ; Birth ; Blood pressure ; Case-Control Studies ; Children ; Data analysis ; Defects ; Echocardiography ; Female ; Fetuses ; Gas exchange ; Gestation ; Heart ; High altitude ; High-altitude environments ; Humans ; Hypertension ; Hypertension, Pulmonary - etiology ; Hypoxia ; Hypoxia - complications ; Hypoxia - physiopathology ; Infant, Newborn ; Investigative techniques of respiratory function ; Investigative techniques, diagnostic techniques (general aspects) ; Laboratories ; Leaves ; Lungs ; Male ; Medical diagnosis ; Medical research ; Medical sciences ; Metabolism ; Neonates ; Nitric Oxide ; Oxygen ; Oxygen content ; Pain perception ; Placenta ; Pulmonary artery ; Pulmonary circulation ; Pulmonary Circulation - physiology ; Pulmonary hypertension ; Pulmonary Wedge Pressure ; Vasoconstriction ; Veins & arteries ; Ventilation ; Young adults</subject><ispartof>The Lancet (British edition), 1999-06, Vol.353 (9171), p.2205-2207</ispartof><rights>1999 Elsevier Ltd</rights><rights>1999 INIST-CNRS</rights><rights>Copyright Lancet Ltd. Jun 26, 1999</rights><rights>Copyright Elsevier Limited Jun 26, 1999</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c445t-8e371c6b6f6f3dc01cfd4dad27759d5a2d69a1acf77cf500a65c56ea849ae2ce3</citedby><cites>FETCH-LOGICAL-c445t-8e371c6b6f6f3dc01cfd4dad27759d5a2d69a1acf77cf500a65c56ea849ae2ce3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0140673698083524$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1860480$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10392986$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sartori, Claudio</creatorcontrib><creatorcontrib>Allemann, Yves</creatorcontrib><creatorcontrib>Trueb, Lionel</creatorcontrib><creatorcontrib>Delabays, Alain</creatorcontrib><creatorcontrib>Nicod, Pascal</creatorcontrib><creatorcontrib>Scherrer, Urs</creatorcontrib><title>Augmented vasoreactivity in adult life associated with perinatal vascular insult</title><title>The Lancet (British edition)</title><addtitle>Lancet</addtitle><description>Adverse environmental events occurring early in life have received little attention as predictors of disease in the later stages of life. At birth, the transition from gas exchange by the placenta to gas exchange by the lungs requires dramatic changes in the pulmonary circulation, which during this period is particularly vulnerable to noxious stimuli. We measured pulmonary-artery pressure responses to high-altitude exposure, a stimulus that causes pronounced pulmonary vasoconstriction, in young adults who had had transient perinatal hypoxic pulmonary hypertension and in controls of similar age and sex distribution.
Review of neonatal-care records at the Lausanne University Hospital for Children identified 15 individuals who met the eligibility criteria (birth at 3·34 weeks of gestation, persistence of hypoxaemia during ventilation with oxygen during the first week of life, and persistence of fetal circulation). Ten of these individuals agreed to take part; the control group was ten volunteers without any history of perinatal complications. Systolic pulmonary-artery pressure (by echocardiography) and arterial oxygen saturation were measured at baseline and at high altitude (4559 m).
The mean increase in pulmonary-artery pressure at high altitude was significantly greater (p=0·01) in the participants who had had perinatal pulmonary hypertension (from 26·2 mm Hg [SD 2·1] to 62·3 mm Hg [7·3]) than in the controls (from 25·8 mm Hg [2·3] to 49·7 mm Hg [11·3]). The fall in arterial oxygen saturation was similar in the two groups.
These findings suggest that a transient perinatal insult to the pulmonary circulation leaves a persistent and potentially fatal imprint, which when activated in adult life predisposes to a pathological response. Survivors of perinatal pulmonary hypertension may be at risk of developing this disorder in later life.</description><subject>Adult</subject><subject>Adults</subject><subject>Age composition</subject><subject>Altitude</subject><subject>Atmospheric pressure</subject><subject>Biological and medical sciences</subject><subject>Birth</subject><subject>Blood pressure</subject><subject>Case-Control Studies</subject><subject>Children</subject><subject>Data analysis</subject><subject>Defects</subject><subject>Echocardiography</subject><subject>Female</subject><subject>Fetuses</subject><subject>Gas exchange</subject><subject>Gestation</subject><subject>Heart</subject><subject>High altitude</subject><subject>High-altitude environments</subject><subject>Humans</subject><subject>Hypertension</subject><subject>Hypertension, Pulmonary - etiology</subject><subject>Hypoxia</subject><subject>Hypoxia - complications</subject><subject>Hypoxia - physiopathology</subject><subject>Infant, Newborn</subject><subject>Investigative techniques of respiratory function</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Laboratories</subject><subject>Leaves</subject><subject>Lungs</subject><subject>Male</subject><subject>Medical diagnosis</subject><subject>Medical research</subject><subject>Medical sciences</subject><subject>Metabolism</subject><subject>Neonates</subject><subject>Nitric Oxide</subject><subject>Oxygen</subject><subject>Oxygen content</subject><subject>Pain perception</subject><subject>Placenta</subject><subject>Pulmonary artery</subject><subject>Pulmonary circulation</subject><subject>Pulmonary Circulation - physiology</subject><subject>Pulmonary hypertension</subject><subject>Pulmonary Wedge Pressure</subject><subject>Vasoconstriction</subject><subject>Veins & arteries</subject><subject>Ventilation</subject><subject>Young 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Urs</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Augmented vasoreactivity in adult life associated with perinatal vascular insult</atitle><jtitle>The Lancet (British edition)</jtitle><addtitle>Lancet</addtitle><date>1999-06-26</date><risdate>1999</risdate><volume>353</volume><issue>9171</issue><spage>2205</spage><epage>2207</epage><pages>2205-2207</pages><issn>0140-6736</issn><eissn>1474-547X</eissn><coden>LANCAO</coden><abstract>Adverse environmental events occurring early in life have received little attention as predictors of disease in the later stages of life. At birth, the transition from gas exchange by the placenta to gas exchange by the lungs requires dramatic changes in the pulmonary circulation, which during this period is particularly vulnerable to noxious stimuli. We measured pulmonary-artery pressure responses to high-altitude exposure, a stimulus that causes pronounced pulmonary vasoconstriction, in young adults who had had transient perinatal hypoxic pulmonary hypertension and in controls of similar age and sex distribution.
Review of neonatal-care records at the Lausanne University Hospital for Children identified 15 individuals who met the eligibility criteria (birth at 3·34 weeks of gestation, persistence of hypoxaemia during ventilation with oxygen during the first week of life, and persistence of fetal circulation). Ten of these individuals agreed to take part; the control group was ten volunteers without any history of perinatal complications. Systolic pulmonary-artery pressure (by echocardiography) and arterial oxygen saturation were measured at baseline and at high altitude (4559 m).
The mean increase in pulmonary-artery pressure at high altitude was significantly greater (p=0·01) in the participants who had had perinatal pulmonary hypertension (from 26·2 mm Hg [SD 2·1] to 62·3 mm Hg [7·3]) than in the controls (from 25·8 mm Hg [2·3] to 49·7 mm Hg [11·3]). The fall in arterial oxygen saturation was similar in the two groups.
These findings suggest that a transient perinatal insult to the pulmonary circulation leaves a persistent and potentially fatal imprint, which when activated in adult life predisposes to a pathological response. Survivors of perinatal pulmonary hypertension may be at risk of developing this disorder in later life.</abstract><cop>London</cop><pub>Elsevier Ltd</pub><pmid>10392986</pmid><doi>10.1016/S0140-6736(98)08352-4</doi><tpages>3</tpages></addata></record> |
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subjects | Adult Adults Age composition Altitude Atmospheric pressure Biological and medical sciences Birth Blood pressure Case-Control Studies Children Data analysis Defects Echocardiography Female Fetuses Gas exchange Gestation Heart High altitude High-altitude environments Humans Hypertension Hypertension, Pulmonary - etiology Hypoxia Hypoxia - complications Hypoxia - physiopathology Infant, Newborn Investigative techniques of respiratory function Investigative techniques, diagnostic techniques (general aspects) Laboratories Leaves Lungs Male Medical diagnosis Medical research Medical sciences Metabolism Neonates Nitric Oxide Oxygen Oxygen content Pain perception Placenta Pulmonary artery Pulmonary circulation Pulmonary Circulation - physiology Pulmonary hypertension Pulmonary Wedge Pressure Vasoconstriction Veins & arteries Ventilation Young adults |
title | Augmented vasoreactivity in adult life associated with perinatal vascular insult |
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