Akoh Christine C, Pressman Eva K, Cooper Elizabeth, Queenan Ruth Anne, Pillittere Julie, O'Brien Kimberly O
1 Division of Nutritional Sciences, Cornell University, Ithaca, NY, USA.
2 Department of Obstetrics and Gynecology, The University of Rochester School of Medicine, Rochester, NY, USA.
Reprod Sci. 2018 Mar;25(3):414-423. doi: 10.1177/1933719117715124. Epub 2017 Jun 15.
Vitamin D is known to regulate innate and adaptive immune processes at the cellular level, but the role of vitamin D status on associated inflammatory processes across pregnancy is unclear. Our primary objective was to evaluate the relationships between serum biomarkers of inflammation (interleukin [IL]-6, IL-10, tumor necrosis factor [TNF]-α), acute-phase proteins (C-reactive protein and hepcidin) and vitamin D status, 25-hydroxyvitamin D (25(OH)D) and 1,25-dihydroxyvitamin D (1,25(OH)D), measured across pregnancy and in the neonate at birth. A second objective was to identify associations between vitamin D status and clinically diagnosed infections. In this study, 158 racially and ethnically diverse pregnant adolescents were recruited from the Rochester Adolescent Maternity Program (RAMP) in Rochester, NY. Serum 1,25(OH)D was significantly lower in adolescents and neonates with IL-6 concentrations above the 75th percentile at delivery ( P = .04) and at birth ( P = .004), respectively. After adjusting for other potential covariates of inflammation, maternal serum 1,25(OH)D was significantly positively associated with TNF-α during pregnancy ( P = .02), but at delivery 1,25(OH)D and TNF-α were inversely associated with one another ( P = .02). Teens with 25(OH)D concentrations <30 ng/mL were more likely to test positive for candida ( P = .002) and bacterial vaginosis ( P = .02) during pregnancy. African Americans exhibited significantly lower TNF-α concentrations at both mid-gestation ( P = .009) and delivery ( P = .001) compared to the Caucasian adolescents. These results suggest that lower maternal vitamin D status may increase risk of infection across gestation.
已知维生素D在细胞水平调节先天性和适应性免疫过程,但维生素D状态在整个孕期相关炎症过程中的作用尚不清楚。我们的主要目标是评估炎症血清生物标志物(白细胞介素[IL]-6、IL-10、肿瘤坏死因子[TNF]-α)、急性期蛋白(C反应蛋白和铁调素)与维生素D状态、25-羟基维生素D(25(OH)D)和1,25-二羟基维生素D(1,25(OH)D)之间的关系,这些指标在孕期及新生儿出生时进行测量。第二个目标是确定维生素D状态与临床诊断感染之间的关联。在本研究中,从纽约罗切斯特的罗切斯特青少年孕产妇项目(RAMP)招募了158名种族和民族多样化的怀孕青少年。分娩时(P = 0.04)和出生时(P = 0.004)IL-6浓度高于第75百分位数的青少年和新生儿血清1,25(OH)D显著降低。在调整其他潜在的炎症协变量后,孕期母体血清1,25(OH)D与TNF-α显著正相关(P = 0.02),但在分娩时1,25(OH)D与TNF-α呈负相关(P = 0.02)。孕期25(OH)D浓度<30 ng/mL的青少年念珠菌检测呈阳性(P = 0.002)和细菌性阴道病检测呈阳性(P = 0.02)的可能性更高。与白人青少年相比,非裔美国人在妊娠中期(P = 0.009)和分娩时(P = 0.001)的TNF-α浓度显著更低。这些结果表明,较低的母体维生素D状态可能会增加整个孕期的感染风险。