Effects of adverse life events on heart rate variability, cortisol, and C-reactive protein

Objective Our objective was to assess whether self‐reported adverse life events during childhood or over the lifespan are associated with altered activity of the autonomic nervous system (ANS), the hypothalamic‐pituitary‐adrenal axis (HPA axis), and the immune system. Method This study was performed...

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Veröffentlicht in:Acta psychiatrica Scandinavica 2015-01, Vol.131 (1), p.40-50
Hauptverfasser: van Ockenburg, S. L., Tak, L. M., Bakker, S. J. L., Gans, R. O. B., de Jonge, P., Rosmalen, J. G. M.
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container_end_page 50
container_issue 1
container_start_page 40
container_title Acta psychiatrica Scandinavica
container_volume 131
creator van Ockenburg, S. L.
Tak, L. M.
Bakker, S. J. L.
Gans, R. O. B.
de Jonge, P.
Rosmalen, J. G. M.
description Objective Our objective was to assess whether self‐reported adverse life events during childhood or over the lifespan are associated with altered activity of the autonomic nervous system (ANS), the hypothalamic‐pituitary‐adrenal axis (HPA axis), and the immune system. Method This study was performed in a population‐based cohort of 1094 adults aged 33–79 years, 46.3% male, average age 53 (SD 11.4). Two waves of data were collected at a 2‐year interval, enabling replication of the analyses. Cumulative exposure to adverse life events was assessed by means of the List of Threatening Experiences. ANS function was assessed by spectral analysis of heart rate variability in the high‐frequency band (HRV‐HF). HPA axis function was assessed by 24‐h urinary free cortisol (24‐h UFC) excretion. Inflammation was assessed by high‐sensitive C‐reactive protein (hsCRP). Results Multiple linear regression analyses did not reveal any significant associations, with the exception of one significant negative association between the lifetime score of adverse life events and HRV‐HF β = −0.028; P = 0.037 at baseline, but not at follow up 2 years later. Conclusion In a large population‐based cohort, adverse life events were not consistently associated with HRV‐HF, 24‐h UFC or (hsCRP).
doi_str_mv 10.1111/acps.12286
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L. ; Tak, L. M. ; Bakker, S. J. L. ; Gans, R. O. B. ; de Jonge, P. ; Rosmalen, J. G. M.</creator><creatorcontrib>van Ockenburg, S. L. ; Tak, L. M. ; Bakker, S. J. L. ; Gans, R. O. B. ; de Jonge, P. ; Rosmalen, J. G. M.</creatorcontrib><description>Objective Our objective was to assess whether self‐reported adverse life events during childhood or over the lifespan are associated with altered activity of the autonomic nervous system (ANS), the hypothalamic‐pituitary‐adrenal axis (HPA axis), and the immune system. Method This study was performed in a population‐based cohort of 1094 adults aged 33–79 years, 46.3% male, average age 53 (SD 11.4). Two waves of data were collected at a 2‐year interval, enabling replication of the analyses. Cumulative exposure to adverse life events was assessed by means of the List of Threatening Experiences. ANS function was assessed by spectral analysis of heart rate variability in the high‐frequency band (HRV‐HF). HPA axis function was assessed by 24‐h urinary free cortisol (24‐h UFC) excretion. Inflammation was assessed by high‐sensitive C‐reactive protein (hsCRP). Results Multiple linear regression analyses did not reveal any significant associations, with the exception of one significant negative association between the lifetime score of adverse life events and HRV‐HF β = −0.028; P = 0.037 at baseline, but not at follow up 2 years later. Conclusion In a large population‐based cohort, adverse life events were not consistently associated with HRV‐HF, 24‐h UFC or (hsCRP).</description><identifier>ISSN: 0001-690X</identifier><identifier>EISSN: 1600-0447</identifier><identifier>DOI: 10.1111/acps.12286</identifier><identifier>PMID: 24833194</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>Adult ; Age Factors ; Aged ; Aged, 80 and over ; autonomic nervous system ; C-reactive protein ; C-Reactive Protein - metabolism ; Chromatography, Liquid - methods ; Cohort Studies ; Cortisol ; Female ; Heart Rate ; heart rate variability ; Hormones ; Humans ; Hydrocortisone - urine ; hypothalamic-pituitary-adrenal axis ; Hypothalamo-Hypophyseal System - metabolism ; Immune system ; Life Change Events ; Male ; Mass Spectrometry - methods ; Middle Aged ; Netherlands ; Neuropsychology ; Pituitary-Adrenal System - metabolism ; Proteins ; Psychiatry ; psychosocial stress ; Retrospective Studies ; Stress, Psychological - blood ; Stress, Psychological - psychology ; Stress, Psychological - urine ; Surveys and Questionnaires</subject><ispartof>Acta psychiatrica Scandinavica, 2015-01, Vol.131 (1), p.40-50</ispartof><rights>2014 John Wiley &amp; Sons A/S. 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L.</creatorcontrib><creatorcontrib>Tak, L. M.</creatorcontrib><creatorcontrib>Bakker, S. J. L.</creatorcontrib><creatorcontrib>Gans, R. O. B.</creatorcontrib><creatorcontrib>de Jonge, P.</creatorcontrib><creatorcontrib>Rosmalen, J. G. M.</creatorcontrib><title>Effects of adverse life events on heart rate variability, cortisol, and C-reactive protein</title><title>Acta psychiatrica Scandinavica</title><addtitle>Acta Psychiatr Scand</addtitle><description>Objective Our objective was to assess whether self‐reported adverse life events during childhood or over the lifespan are associated with altered activity of the autonomic nervous system (ANS), the hypothalamic‐pituitary‐adrenal axis (HPA axis), and the immune system. Method This study was performed in a population‐based cohort of 1094 adults aged 33–79 years, 46.3% male, average age 53 (SD 11.4). Two waves of data were collected at a 2‐year interval, enabling replication of the analyses. Cumulative exposure to adverse life events was assessed by means of the List of Threatening Experiences. ANS function was assessed by spectral analysis of heart rate variability in the high‐frequency band (HRV‐HF). HPA axis function was assessed by 24‐h urinary free cortisol (24‐h UFC) excretion. Inflammation was assessed by high‐sensitive C‐reactive protein (hsCRP). Results Multiple linear regression analyses did not reveal any significant associations, with the exception of one significant negative association between the lifetime score of adverse life events and HRV‐HF β = −0.028; P = 0.037 at baseline, but not at follow up 2 years later. Conclusion In a large population‐based cohort, adverse life events were not consistently associated with HRV‐HF, 24‐h UFC or (hsCRP).</description><subject>Adult</subject><subject>Age Factors</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>autonomic nervous system</subject><subject>C-reactive protein</subject><subject>C-Reactive Protein - metabolism</subject><subject>Chromatography, Liquid - methods</subject><subject>Cohort Studies</subject><subject>Cortisol</subject><subject>Female</subject><subject>Heart Rate</subject><subject>heart rate variability</subject><subject>Hormones</subject><subject>Humans</subject><subject>Hydrocortisone - urine</subject><subject>hypothalamic-pituitary-adrenal axis</subject><subject>Hypothalamo-Hypophyseal System - metabolism</subject><subject>Immune system</subject><subject>Life Change Events</subject><subject>Male</subject><subject>Mass Spectrometry - methods</subject><subject>Middle Aged</subject><subject>Netherlands</subject><subject>Neuropsychology</subject><subject>Pituitary-Adrenal System - metabolism</subject><subject>Proteins</subject><subject>Psychiatry</subject><subject>psychosocial stress</subject><subject>Retrospective Studies</subject><subject>Stress, Psychological - blood</subject><subject>Stress, Psychological - psychology</subject><subject>Stress, Psychological - urine</subject><subject>Surveys and Questionnaires</subject><issn>0001-690X</issn><issn>1600-0447</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU1P3DAQhq2qVdlCL_0ByFIvqCJgx46dHCGi9AP1QwUt6sWaOBNhmk0W27vt_vs6XeDQQ9W5jGb0zDt69RLyirMjnuoY7DIc8Twv1RMy44qxjEmpn5IZY4xnqmLXO-RFCLdpLDgrn5OdXJZC8ErOyPezrkMbAx07Cu0afUDauw4prnGY1gO9QfCReohI1-AdNK53cXNI7eijC2N_SGFoaZ15BBvdGunSjxHdsEeeddAHfHnfd8nV27PL-l128fn8fX1ykVlZlSoTqAvQjQSpoVGFtJUGZE2ucoRK5GWbttrqrm1tqYRuCp18tLwQ08iEELvkYKub_t6tMESzcMFi38OA4yoYrqRmXAsl_wMVulC51hP6-i_0dlz5IRmZKMWEKnKVqDdbyvoxBI-dWXq3AL8xnJkpHDOFY_6Ek-D9e8lVs8D2EX1IIwF8C_x0PW7-IWVO6i_fHkSz7Y0LEX893oD_YZRObsz807n5cP1xzr7Oa3MqfgNFeqcu</recordid><startdate>201501</startdate><enddate>201501</enddate><creator>van Ockenburg, S. L.</creator><creator>Tak, L. M.</creator><creator>Bakker, S. J. L.</creator><creator>Gans, R. O. B.</creator><creator>de Jonge, P.</creator><creator>Rosmalen, J. G. M.</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>201501</creationdate><title>Effects of adverse life events on heart rate variability, cortisol, and C-reactive protein</title><author>van Ockenburg, S. L. ; Tak, L. M. ; Bakker, S. J. L. ; Gans, R. O. B. ; de Jonge, P. ; Rosmalen, J. G. 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L.</creatorcontrib><creatorcontrib>Tak, L. M.</creatorcontrib><creatorcontrib>Bakker, S. J. L.</creatorcontrib><creatorcontrib>Gans, R. O. B.</creatorcontrib><creatorcontrib>de Jonge, P.</creatorcontrib><creatorcontrib>Rosmalen, J. G. M.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Acta psychiatrica Scandinavica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>van Ockenburg, S. L.</au><au>Tak, L. M.</au><au>Bakker, S. J. L.</au><au>Gans, R. O. B.</au><au>de Jonge, P.</au><au>Rosmalen, J. G. M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of adverse life events on heart rate variability, cortisol, and C-reactive protein</atitle><jtitle>Acta psychiatrica Scandinavica</jtitle><addtitle>Acta Psychiatr Scand</addtitle><date>2015-01</date><risdate>2015</risdate><volume>131</volume><issue>1</issue><spage>40</spage><epage>50</epage><pages>40-50</pages><issn>0001-690X</issn><eissn>1600-0447</eissn><abstract>Objective Our objective was to assess whether self‐reported adverse life events during childhood or over the lifespan are associated with altered activity of the autonomic nervous system (ANS), the hypothalamic‐pituitary‐adrenal axis (HPA axis), and the immune system. Method This study was performed in a population‐based cohort of 1094 adults aged 33–79 years, 46.3% male, average age 53 (SD 11.4). Two waves of data were collected at a 2‐year interval, enabling replication of the analyses. Cumulative exposure to adverse life events was assessed by means of the List of Threatening Experiences. ANS function was assessed by spectral analysis of heart rate variability in the high‐frequency band (HRV‐HF). HPA axis function was assessed by 24‐h urinary free cortisol (24‐h UFC) excretion. Inflammation was assessed by high‐sensitive C‐reactive protein (hsCRP). Results Multiple linear regression analyses did not reveal any significant associations, with the exception of one significant negative association between the lifetime score of adverse life events and HRV‐HF β = −0.028; P = 0.037 at baseline, but not at follow up 2 years later. Conclusion In a large population‐based cohort, adverse life events were not consistently associated with HRV‐HF, 24‐h UFC or (hsCRP).</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>24833194</pmid><doi>10.1111/acps.12286</doi><tpages>11</tpages></addata></record>
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source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Adult
Age Factors
Aged
Aged, 80 and over
autonomic nervous system
C-reactive protein
C-Reactive Protein - metabolism
Chromatography, Liquid - methods
Cohort Studies
Cortisol
Female
Heart Rate
heart rate variability
Hormones
Humans
Hydrocortisone - urine
hypothalamic-pituitary-adrenal axis
Hypothalamo-Hypophyseal System - metabolism
Immune system
Life Change Events
Male
Mass Spectrometry - methods
Middle Aged
Netherlands
Neuropsychology
Pituitary-Adrenal System - metabolism
Proteins
Psychiatry
psychosocial stress
Retrospective Studies
Stress, Psychological - blood
Stress, Psychological - psychology
Stress, Psychological - urine
Surveys and Questionnaires
title Effects of adverse life events on heart rate variability, cortisol, and C-reactive protein
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