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Pathogen burden and cortisol profiles over the day
Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Kemiska institutionen.ORCID-id: 0000-0001-8632-7087
Umeå universitet, Medicinska fakulteten, Institutionen för molekylärbiologi (Medicinska fakulteten).
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2009 (Engelska)Ingår i: Epidemiology and Infection, ISSN 0950-2688, E-ISSN 1469-4409, Vol. 137, nr 12, s. 1816-1824Artikel i tidskrift (Refereegranskat) Published
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Abstract [en]

Hypothalamic-pituitary-adrenocortical (HPA) regulation in adults is influenced by early psychosocial adversity, but the role of infectious disease history is poorly understood. We studied the association between cumulative pathogen burden and cortisol profile over the day in a sample of 317 healthy men and women aged 51-72 years. Cumulative pathogen burden was defined as positive serostatus for Chlamydia pneumoniae, cytomegalovirus (CMV) and herpes simplex virus 1 (HSV-1). Salivary cortisol was sampled repeatedly over the day. The cortisol slope was defined as the decrease across the day and evening. Age, gender, grade of employment, body mass index, smoking status, self-rated health, cardiovascular medication, depressed mood and time of waking were included as covariates. The pathogen burden averaged 1.76 (S.D. = 0.92). The cortisol slope was inversely associated with pathogen burden after controlling for covariates. When individual pathogens were studied, only CMV was associated with flatter cortisol rhythms in isolation. We conclude that pathogen burden is independently associated with flatter cortisol slopes over the day, and may contribute to disturbed neuroendocrine regulation.

Ort, förlag, år, upplaga, sidor
New York: Cambridge University Press, 2009. Vol. 137, nr 12, s. 1816-1824
Nyckelord [en]
Cortisol awakening response, Chlamydia pneumoniae, cytomegalovirus, herpes simplex virus 1, psychosocial adversity
Nationell ämneskategori
Folkhälsovetenskap, global hälsa och socialmedicin Infektionsmedicin
Identifikatorer
URN: urn:nbn:se:umu:diva-115946DOI: 10.1017/S0950268809002738ISI: 000271971400022PubMedID: 19450380Scopus ID: 2-s2.0-70449715491OAI: oai:DiVA.org:umu-115946DiVA, id: diva2:907872
Tillgänglig från: 2016-03-01 Skapad: 2016-02-08 Senast uppdaterad: 2025-02-20Bibliografiskt granskad

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Gylfe, ÅsaBergström, Sven

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Gylfe, ÅsaBergström, Sven
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Kemiska institutionenInstitutionen för molekylärbiologi (Medicinska fakulteten)
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Epidemiology and Infection
Folkhälsovetenskap, global hälsa och socialmedicinInfektionsmedicin

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