Ebersole Jeffrey L, Novak M John, Michalowicz Bryan S, Hodges James S, Steffen Michelle J, Ferguson James E, Diangelis Anthony, Buchanan William, Mitchell Dennis A, Papapanou Panos N
Center for Oral Health Research and Department of Obstetrics and Gynecology, University of Kentucky, Lexington, KY, USA.
J Periodontol. 2009 Jun;80(6):953-60. doi: 10.1902/jop.2009.080464.
Our previous studies reported on the obstetric, periodontal, and microbiologic outcomes of women participating in the Obstetrics and Periodontal Therapy (OPT) Study. This article describes the systemic antibody responses to selected periodontal bacteria in the same patients.
Serum samples, obtained from pregnant women at baseline (13 to 16 weeks; 6 days of gestation) and 29 to 32 weeks, were analyzed by enzyme-linked immunosorbent assay for serum immunoglobulin G (IgG) antibody to Aggregatibacter actinomycetemcomitans (previously Actinobacillus actinomycetemcomitans), Campylobacter rectus, Fusobacterium nucleatum, Porphyromonas gingivalis, Prevotella intermedia, Tannerella forsythia (previously T. forsythensis), and Treponema denticola.
At baseline, women who delivered live preterm infants had significantly lower total serum levels of IgG antibody to the panel of periodontal pathogens (P = 0.0018), to P. gingivalis (P = 0.0013), and to F. nucleatum (P = 0.0200) than women who delivered at term. These differences were not significant at 29 to 32 weeks. Changes in IgG levels between baseline and 29 to 32 weeks were not associated with preterm birth when adjusted for treatment group, clinical center, race, or age. In addition, delivery of low birth weight infants was not associated with levels of antibody at baseline or with antibody changes during pregnancy.
Live preterm birth is associated with decreased levels of IgG antibody to periodontal pathogens in women with periodontitis when assessed during the second trimester. Changes in IgG antibody during pregnancy are not associated with birth outcomes.
我们之前的研究报告了参与产科与牙周治疗(OPT)研究的女性的产科、牙周及微生物学结局。本文描述了同一批患者对选定牙周细菌的全身抗体反应。
通过酶联免疫吸附测定法分析从孕妇孕早期(13至16周;妊娠6天)和孕29至32周时采集的血清样本,检测针对伴放线聚集杆菌(以前称为伴放线放线杆菌)、直肠弯曲菌、具核梭杆菌、牙龈卟啉单胞菌、中间普氏菌、福赛坦纳菌(以前称为福赛坦氏菌)和齿垢密螺旋体的血清免疫球蛋白G(IgG)抗体。
在孕早期,分娩活产早产儿的女性血清中针对牙周病原体组、牙龈卟啉单胞菌及具核梭杆菌的IgG抗体总水平显著低于足月分娩的女性(P = 0.0018、P = 0.0013、P = 0.0200)。在孕29至32周时,这些差异不显著。在校正治疗组、临床中心、种族或年龄后,孕早期与孕29至32周之间IgG水平的变化与早产无关。此外,低出生体重儿的分娩与孕早期抗体水平或孕期抗体变化无关。
在孕中期评估时,早产与牙周炎女性针对牙周病原体的IgG抗体水平降低有关。孕期IgG抗体变化与出生结局无关。