PMID- 18308510 OWN - NLM STAT- MEDLINE DCOM- 20080812 LR - 20211020 IS - 1090-2139 (Electronic) IS - 0889-1591 (Print) IS - 0889-1591 (Linking) VI - 22 IP - 6 DP - 2008 Aug TI - The associations between psychosocial stress and the frequency of illness, and innate and adaptive immune function in children. PG - 933-40 LID - 10.1016/j.bbi.2008.01.007 [doi] AB - OBJECTIVE: Family processes have a substantial impact on children's social and emotional well-being, but little is known about the effects of family stress on children's physical health. To begin to identify potential links between family stress and health in children, we examined associations between specific aspects of family psychosocial stress and the frequency of illnesses in children, measures of innate and adaptive immune function, and human herpesvirus 6 (HHV-6) reactivation. STUDY DESIGN: Prospective study of 169 ambulatory school-age children and parents. Parents completed multiple assessments of stress at 7 sequential six-month visits and maintained weekly illness diaries for their children over three years using a thermometer to record fever. Children had blood obtained for HHV-6 and immune function studies at each visit including natural killer (NK) cell function and the percentage of CD4 and CD8 cells associated with immune control of cytomegalovirus (CMV). RESULTS: Parental psychiatric symptoms were associated with a higher frequency of illnesses: for each 1 U increase in symptom score children had an increased 1-year rate of total illnesses of 40% (rate ratio, 1.40; 95% CI, 1.06-1.85) and febrile illnesses of 77% (rate ratio, 1.77, 95% CI, 1.00-3.13). Parental psychiatric symptom scores were also associated with enhanced NK cell function (estimate, 0.15; 95% CI, 0.05-0.26) and increased percentages of CD8+CD28-CD57+ cells in the blood of CMV seropositive children (estimate, 2.57; 95% CI, 0.36-4.79). HHV-6 reactivation was not detected. CONCLUSIONS: There is an association between specific psychosocial stress exposure and rates of illness and immune function in normally developing children. FAU - Caserta, Mary T AU - Caserta MT AD - Department of Pediatrics, University of Rochester School of Medicine and Dentistry, Rochester, NY 14642, USA. mary_caserta@urmc.rochester.edu FAU - O'Connor, Thomas G AU - O'Connor TG FAU - Wyman, Peter A AU - Wyman PA FAU - Wang, Hongyue AU - Wang H FAU - Moynihan, Jan AU - Moynihan J FAU - Cross, Wendi AU - Cross W FAU - Tu, Xin AU - Tu X FAU - Jin, Xia AU - Jin X LA - eng GR - R01 HD038938-01A1/HD/NICHD NIH HHS/United States GR - 5 MO1 RR00044/RR/NCRR NIH HHS/United States GR - R01 HD 38938/HD/NICHD NIH HHS/United States GR - 1 UL1 RR024160-01/RR/NCRR NIH HHS/United States GR - M01 RR000044/RR/NCRR NIH HHS/United States GR - UL1 RR024160/RR/NCRR NIH HHS/United States GR - R01 HD038938/HD/NICHD NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Extramural DEP - 20080304 PL - Netherlands TA - Brain Behav Immun JT - Brain, behavior, and immunity JID - 8800478 SB - IM MH - CD4-Positive T-Lymphocytes/immunology MH - CD8-Positive T-Lymphocytes/immunology MH - Child MH - Child, Preschool MH - Cytomegalovirus/immunology MH - Family Health MH - Female MH - Herpesvirus 6, Human/immunology MH - Humans MH - Immunity/*physiology MH - Immunity, Innate/physiology MH - Killer Cells, Natural/immunology MH - Male MH - *Parent-Child Relations MH - Parents/*psychology MH - Prospective Studies MH - Stress, Psychological/*immunology MH - Surveys and Questionnaires PMC - PMC2516370 MID - NIHMS59850 EDAT- 2008/03/01 09:00 MHDA- 2008/08/13 09:00 PMCR- 2009/08/01 CRDT- 2008/03/01 09:00 PHST- 2007/09/22 00:00 [received] PHST- 2008/01/15 00:00 [revised] PHST- 2008/01/15 00:00 [accepted] PHST- 2008/03/01 09:00 [pubmed] PHST- 2008/08/13 09:00 [medline] PHST- 2008/03/01 09:00 [entrez] PHST- 2009/08/01 00:00 [pmc-release] AID - S0889-1591(08)00032-9 [pii] AID - 10.1016/j.bbi.2008.01.007 [doi] PST - ppublish SO - Brain Behav Immun. 2008 Aug;22(6):933-40. doi: 10.1016/j.bbi.2008.01.007. Epub 2008 Mar 4.