Haynes Robin L, Folkerth Rebecca D, Paterson David S, Broadbelt Kevin G, Dan Zaharie S, Hewlett Richard H, Dempers Johan J, Burger Elsie, Wadee Shabbir, Schubert Pawel, Wright Colleen, Sens Mary Ann, Nelsen Laura, Randall Bradley B, Tran Hoa, Geldenhuys Elaine, Elliott Amy J, Odendaal Hein J, Kinney Hannah C
From the Department of Pathology, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts (RLH, RDF, DSP, KGB, HT, HCK); Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts (RDF); Department of Pathology, Faculty of Medicine and Health Science, Stellenbosch University, Western Cape, South Africa ((SDZ, RHH, PS, EG); Division of Forensic Pathology and Medicine, Department of Pathology and Western Cape Forensic Pathology Services, Health Science Faculty, Stellenbosch University, Cape Town, South Africa (JJD, EB, SW); National Health Laboratory Services, Port Elizabeth, Eastern Cape, South Africa (CW); Department of Pathology, University of North Dakota, Grand Forks, North Dakota (MAS); Department of Pathology, University of South Dakota School of Medicine, Sioux Falls, South Dakota (LN, BBR); Community and Population Health Sciences, Sanford Research, Sioux Falls, South Dakota (AJE); Department of Obstetrics and Gynecology, Faculty of Medicine and Health Science, Stellenbosch University, Western Cape, South Africa (HJO); The Prenatal Alcohol, SIDS, and Stillbirth (PASS) Research Network (PN).
J Neuropathol Exp Neurol. 2016 Nov 1;75(11):1048-1057. doi: 10.1093/jnen/nlw080.
The Safe Passage Study is an international, prospective study of approximately 12 000 pregnancies to determine the effects of prenatal alcohol exposure (PAE) upon stillbirth and the sudden infant death syndrome (SIDS). A key objective of the study is to elucidate adverse effects of PAE upon binding to serotonin (5-HT) 1A receptors in brainstem homeostatic networks postulated to be abnormal in unexplained stillbirth and/or SIDS. We undertook a feasibility assessment of 5-HT1A receptor binding using autoradiography in the medulla oblongata (6 nuclei in 27 cases). 5-HT1A binding was compared to a reference dataset from the San Diego medical examiner's system. There was no adverse effect of postmortem interval ≤100 h. The distribution and quantitated values of 5-HT1A binding in Safe Passage Study cases were essentially identical to those in the reference dataset, and virtually identical between stillbirths and live born fetal cases in grossly non-macerated tissues. The pattern of binding was present at mid-gestation with dramatic changes in binding levels in the medullary 5-HT nuclei over the second half of gestation; there was a plateau at lower levels in the neonatal period and into infancy. This study demonstrates feasibility of 5-HT1A binding analysis in the medulla in the Safe Passage Study.
“安全通道研究”是一项国际性前瞻性研究,涉及约12000例妊娠,旨在确定产前酒精暴露(PAE)对死产和婴儿猝死综合征(SIDS)的影响。该研究的一个关键目标是阐明PAE对脑干稳态网络中与5-羟色胺(5-HT)1A受体结合的不利影响,据推测,在不明原因的死产和/或SIDS中,该网络是异常的。我们使用放射自显影术对延髓(27例中的6个核)进行了5-HT1A受体结合的可行性评估。将5-HT1A结合情况与圣地亚哥法医系统的参考数据集进行了比较。死后间隔≤100小时没有不利影响。“安全通道研究”病例中5-HT1A结合的分布和定量值与参考数据集中的基本相同,在严重未浸软的组织中,死产和活产胎儿病例之间几乎相同。结合模式在妊娠中期出现,在妊娠后半期延髓5-HT核中的结合水平发生显著变化;在新生儿期和婴儿期,结合水平较低并保持稳定。这项研究证明了在“安全通道研究”中对延髓进行5-HT1A结合分析的可行性。