Disorders of placental villous maturation are present in one-third of cases with spontaneous preterm labor

被引:25
作者
Jaiman, Sunil [2 ,3 ]
Romero, Roberto [1 ]
Pacora, Percy [2 ,4 ]
Erez, Offer [2 ,5 ]
Jung, Eunjung [2 ,4 ]
Tarca, Adi L. [2 ,4 ,6 ]
Bhatti, Gaurav [2 ,4 ]
Yeo, Lami [2 ,4 ]
Kim, Yeon Mee [2 ,7 ]
Kim, Chong Jai [2 ,8 ]
Kim, Jung-Sun [2 ,9 ]
Qureshi, Faisal [2 ,3 ,10 ]
Jacques, Suzanne M. [2 ,3 ,10 ]
Gomez-Lopez, Nardhy [2 ,11 ]
Hsu, Chaur-Dong [4 ,12 ]
机构
[1] Wayne State Univ, Perinatol Res Branch, NICHD, NIH,DHHS, 3990 John R,Box 4, Detroit, MI 48201 USA
[2] Eunice Kennedy Shriver Natl Inst Child Hlth & Hum, Perinatol Res Branch, Div Obstet & Maternal Fetal Med, Div Intramural Res,NIH,US Dept HHS, Bethesda, MD USA
[3] Wayne State Univ, Sch Med, Dept Pathol, Hutzel Womens Hosp, Detroit, MI 48201 USA
[4] Wayne State Univ, Sch Med, Dept Obstet & Gynecol, Detroit, MI 48201 USA
[5] Ben Gurion Univ Negev, Soroka Univ, Fac Hlth Sci, Med Ctr,Dept Obstet & Gynecol,Sch Med, Beer Sheva, Israel
[6] Wayne State Univ, Dept Comp Sci, Coll Engn, Detroit, MI 48202 USA
[7] Inje Univ, Haeundae Paik Hosp, Coll Med, Dept Pathol, Busan, South Korea
[8] Univ Ulsan, Asan Med Ctr, Dept Pathol, Coll Med, Seoul, South Korea
[9] Sungkyunkwan Univ, Samsung Med Ctr, Dept Pathol, Sch Med, Seoul, South Korea
[10] Harper Univ Hosp, Dept Pathol, Detroit, MI USA
[11] Wayne State Univ, Sch Med, Dept Biochem Microbiol & Immunol, Detroit, MI USA
[12] Wayne State Univ, Sch Med, Dept Physiol, Detroit, MI 48201 USA
基金
美国国家卫生研究院;
关键词
accelerated villous maturation; acute placental inflammation; chronic placental inflammation; delayed villous maturation; hypercapillarized villi; maternal anti-fetal rejection; maternal-fetal inflammatory response; maternal vascular malperfusion; nucleated red blood cells; placental pathology; RED-BLOOD-CELLS; FOR-GESTATIONAL-AGE; MATERNAL FLOOR INFARCTION; ENDOTHELIAL GROWTH-FACTOR; PREMATURE RUPTURE; TERM INFANTS; PHYSIOLOGICAL TRANSFORMATION; CLINICAL CHARACTERISTICS; CHRONIC CHORIOAMNIONITIS; PATHOLOGICAL FEATURES;
D O I
10.1515/jpm-2020-0138
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objectives: Spontaneous preterm labor is an obstetrical syndrome accounting for approximately 65-70% of preterm births, the latter being the most frequent cause of neonatal death and the second most frequent cause of death in children less than five years of age worldwide. The purpose of this study was to determine and compare to uncomplicated pregnancies (1) the frequency of placental disorders of villous maturation in spontaneous preterm labor; (2) the frequency of other placental morphologic characteristics associated with the preterm labor syndrome; and (3) the distribution of these lesions according to gestational age at delivery and their severity. Methods: A case-control study of singleton pregnant women was conducted that included (1) uncomplicated pregnancies (controls, n=944) and (2) pregnancies with spontaneous preterm labor (cases, n=438). All placentas underwent histopathologic examination. Patients with chronic maternal diseases (e.g., chronic hypertension, diabetes mellitus, renal disease, thyroid disease, asthma, autoimmune disease, and coagulopathies), fetal malformations, chromosomal abnormalities, multifetal gestation, preeclampsia, eclampsia, preterm prelabor rupture of the fetal membranes, gestational hypertension, gestational diabetes mellitus, and HELLP (hemolysis, elevated liver enzymes and low platelet count) syndrome were excluded from the study. Results: Compared to the controls, the most prevalent placental lesions among the cases were the disorders of villous maturation (31.8% [106/333] including delayed villous maturation 18.6% [62/333] vs. 1.4% [6/442], q<0.0001, prevalence ratio 13.7; and accelerated villous maturation 13.2% [44/333] vs. 0%[0/442], q<0.001). Other lesions in decreasing order of prevalence included hypercapillarized villi (15.6% [68/435] vs. 3.5% [33/938], q<0.001, prevalence ratio 4.4); nucleated red blood cells (1.1% [5/437] vs. 0% [0/938], q<0.01); chronic inflammatory lesions (47.9% [210/438] vs. 29.9% [282/944], q<0.0001, prevalence ratio 1.6); fetal inflammatory response (30.1% [132/438] vs. 23.2% [219/944], q<0.05, prevalence ratio 1.3); maternal inflammatory response (45.5% [195/438] vs. 36.1% [341/944], q<0.01, prevalence ratio 1.2); and maternal vascular malperfusion (44.5% [195/438] vs. 35.7% [337/944], q<0.01, prevalence ratio 1.2). Accelerated villous maturation did not show gestational age-dependent association with any other placental lesion while delayed villous maturation showed a gestational age-dependent association with acute placental inflammation (q-value=0.005). Conclusions: Disorders of villous maturation are present in nearly one-third of the cases of spontaneous preterm labor.
引用
收藏
页码:412 / 430
页数:19
相关论文
共 151 条
[11]  
[Anonymous], 2017, AM J OBSTET GYNECOL, DOI DOI 10.1016/J.AJ0G.2016.12.022
[12]   MATERNAL PLACENTAL VASCULOPATHY AND INFECTION - 2 DISTINCT SUBGROUPS AMONG PATIENTS WITH PRETERM LABOR AND PRETERM RUPTURED MEMBRANES [J].
ARIAS, F ;
RODRIQUEZ, L ;
RAYNE, SC ;
KRAUS, FT .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1993, 168 (02) :585-591
[13]   Placental histology and clinical characteristics of patients with preterm premature rupture of membranes [J].
Arias, F ;
Victoria, A ;
Cho, K ;
Kraus, F .
OBSTETRICS AND GYNECOLOGY, 1997, 89 (02) :265-271
[14]  
Becker V., 1981, PLAZENTA MENSCHEN
[15]   Nucleated red blood cells and fetal hypoxia: a biologic marker whose 'timing' has come? [J].
Bedrick, A. D. .
JOURNAL OF PERINATOLOGY, 2014, 34 (02) :85-86
[16]  
Benirschke K., 2006, Pathology of the Human Placenta, P321
[17]  
Benirschke K., 1990, PATHOLOGY HUMAN PLAC
[18]   CONTROLLING THE FALSE DISCOVERY RATE - A PRACTICAL AND POWERFUL APPROACH TO MULTIPLE TESTING [J].
BENJAMINI, Y ;
HOCHBERG, Y .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 1995, 57 (01) :289-300
[19]   Running throughout pregnancy: Effect on placental villous vascular volume and cell proliferation [J].
Bergmann, A ;
Clapp, JF ;
Zygmunt, M .
PLACENTA, 2004, 25 (8-9) :A15-A15
[20]   Timing of fetal nucleated red blood cell count elevation in response to acute hypoxia [J].
Blackwell, SC ;
Hallak, M ;
Hotra, JW ;
Refuerzo, J ;
Hassan, SS ;
Sokol, RJ ;
Sorokin, Y .
BIOLOGY OF THE NEONATE, 2004, 85 (04) :217-220