In the initial funding period (1992-6) we found that mothers of very low birthweight infants (VLBW;< 1500 grams) have depressed lymphocyte proliferation and lower levels of some immune cell subsets compared to mothers of term infants in the first four postpartal months. Additionally, mothers of VLBW infants have higher anxiety, and anxiety in the early postpartum, is related to depressed immune function. If increased stress (including anxiety) and depressed immune function are related to detrimental changes in maternal and infant health, nursing interventions to improve the health of mothers and their VLBW infants could be designed and tested. These interventions could include efforts to decrease maternal and infant exposure to infection or other actions directed toward improving immune function such as decreasing fatigue, improving nutrition and exercise, or using relaxation techniques. Although differences in health behaviors did not account for differences between mothers of term and VLBW infants in immune response in our ongoing work, these health behaviors might make an important independent contribution to differences in health outcomes for mothers and their VLBW babies. In this phase, three groups of subjects (mothers of VLBW infants, mothers of term infants, and nonpostpartal women) will be compared to determine if stress and the depressed immune response we have documented are related to health outcomes. We will control for levels of sex hormones which may have an independent influence on immune status. Stress will be measured by: anxiety (Multiple Affect Adjective Checklist), daily hassles (Daily Hassles Scale), and serum cortisol levels. Changes in immune profile will be determined by lymphocyte and monocyte subset analysis using flow cytometry. Immune function will be measured in a subset of mothers using the lymphocyte proliferative response to mitogens and antigen recall. Prolactin and estrogen levels will be measured using single antibody RIA. Adult health will be measured by the Monthly Health Review and maternal interview. Infant health will be measured by: maternal interview, chart review, growth, and development using the Bayley Scales of Infant Development. This study will provide information about postpartal immune status necessary in targeting prophylactic nursing interventions for both mothers and their VLBW infants.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
3M01RR000040-37S4
Application #
2757429
Study Section
Project Start
Project End
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
37
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of Pennsylvania
Department
Type
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Khalili, Mandana; Shuhart, Margaret C; Lombardero, Manuel et al. (2018) Relationship Between Metabolic Syndrome, Alanine Aminotransferase Levels, and Liver Disease Severity in a Multiethnic North American Cohort With Chronic Hepatitis B. Diabetes Care 41:1251-1259
Thomas, Bernadette; Matsushita, Kunihiro; Abate, Kalkidan Hassen et al. (2017) Global Cardiovascular and Renal Outcomes of Reduced GFR. J Am Soc Nephrol 28:2167-2179
Ojiro, Keisuke; Qu, Xiaowang; Cho, Hyosun et al. (2017) Modulation of Hepatitis C Virus-Specific CD8 Effector T-Cell Function with Antiviral Effect in Infectious Hepatitis C Virus Coculture Model. J Virol 91:
Di Bisceglie, A M; Lombardero, M; Teckman, J et al. (2017) Determination of hepatitis B phenotype using biochemical and serological markers. J Viral Hepat 24:320-329
Lok, A S; Ganova-Raeva, L; Cloonan, Y et al. (2017) Prevalence of hepatitis B antiviral drug resistance variants in North American patients with chronic hepatitis B not receiving antiviral treatment. J Viral Hepat 24:1032-1042
Evon, Donna M; Wahed, Abdus S; Johnson, Geoffrey et al. (2016) Fatigue in Patients with Chronic Hepatitis B Living in North America: Results from the Hepatitis B Research Network (HBRN). Dig Dis Sci 61:1186-96
Park, Jang-June; Wong, David K; Wahed, Abdus S et al. (2016) Hepatitis B Virus--Specific and Global T-Cell Dysfunction in Chronic Hepatitis B. Gastroenterology 150:684-695.e5
Hering, Bernhard J; Clarke, William R; Bridges, Nancy D et al. (2016) Phase 3 Trial of Transplantation of Human Islets in Type 1 Diabetes Complicated by Severe Hypoglycemia. Diabetes Care 39:1230-40
Leonard, Mary B; Shults, Justine; Long, Jin et al. (2016) Effect of Low-Magnitude Mechanical Stimuli on Bone Density and Structure in Pediatric Crohn's Disease: A Randomized Placebo-Controlled Trial. J Bone Miner Res 31:1177-88
Ricordi, Camillo; Goldstein, Julia S; Balamurugan, A N et al. (2016) National Institutes of Health-Sponsored Clinical Islet Transplantation Consortium Phase 3 Trial: Manufacture of a Complex Cellular Product at Eight Processing Facilities. Diabetes 65:3418-3428

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