Systemic Inflammation in the Extremely Low Gestational Age Newborn Following Maternal Genitourinary Infections. (28th August 2014)

• Record Type: Journal Article
• Authors: Fichorova, Raina N.; Beatty, Noah; Sassi, Rita R. S.; Yamamoto, Hidemi S.; Allred, Elizabeth N.; Leviton, Alan; the ELGAN investigators
• Is Part Of: American journal of reproductive immunology. Volume 73:Number 2(2015:Feb.)
• Page Start: 162
• Page End: 174
• Publication Date: 2014-08-28
• Subjects: Human reproduction -- Immunological aspects -- Periodicals; 616.69206
• DOI: 10.1111/aji.12313
• Languages: English
• ISSNs: 1046-7408

Abstract

<abstract abstract-type="main" id="aji12313-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="aji12313-sec-0001" sec-type="section"> <title>Problem</title> <p>Gestational genitourinary infections are associated with lifelong disabilities<bold>, </bold> but it is unknown if neonatal inflammation is involved.</p> </sec> <sec id="aji12313-sec-0002" sec-type="section"> <title>Method</title> <p>Mothers of 914 infants born before 28th gestation week reported cervical/vaginal infection (CVI), and/or urine/bladder/kidney infection (UTI), or neither. Inflammation proteins measured in baby's blood on postnatal days 1, 7, and 14 were considered elevated if in the top quartile for gestational age. Logistic regression models adjusting for potential confounders assessed odds ratios.</p> </sec> <sec id="aji12313-sec-0003" sec-type="section"> <title>Results</title> <p>Compared to mothers with neither UTI/CVI, those with CVI were more likely to have infants with elevated CRP, SAA, MPO, IL‐1β, IL‐6, IL‐6R, TNF‐α, RANTES, ICAM‐3, E‐selectin, and VEGF‐R2 on day 1; those with UTI were more likely to have infants with elevated MPO, IL‐6R, TNF‐R1, TNF‐R2, and RANTES on day 7. Placental anaerobes and genital mycoplasma were more common in pregnancies with CVI.</p> </sec> <sec id="aji12313-sec-0004" sec-type="section"> <title>Conclusion</title> <p>Gestational UTI/CVI should be targeted for preventing systemic inflammation in the very preterm newborn.</p> </sec> </abstract>