Sonographic measurement of the fetal thymus: Relationship with maternal obesity.

BACKGROUND: The purpose of this study was to evaluate the influence of maternal obesity on the size of the fetal thymus. METHODS: The study population consisted of 138 pregnant women who were divided into two groups based on their body mass index (BMI): Normal-weight group (n = 97; BMI: 18-25 kg/m2 ) and obese group (n = 41; BMI: ≥ 30 kg/m2 ). All participants underwent routine second-trimester prenatal ultrasound (US) screening at 20-25 weeks of gestation. Differences in US measurement of fetal thymus, fetal anthropometric measurements, subcutaneous adipose tissue thickness, fetal weight, gestational age, white blood cell count, and C-reactive protein (CRP) values between groups were compared. RESULTS: The mean thymus size was 18.7 ± 2.9 mm for normal-weight group, and 21.6 ± 3.7 mm for the obese group (p < 0.001). CRP values were also significantly different between groups (6.8 ± 4.4 mg/dl for normal-weight group, 14.8 ± 1.8 mg/dl for obese group, p < 0.001). CONCLUSIONS: Fetal thymus size was increased in obese women, and this increase may indicate immunologic abnormalities in fetuses. However, future large-scale studies are necessary to support this association. © 2016 Wiley Periodicals, Inc. J Clin Ultrasound 45:277-281, 2017.

Evaluation of oxidative stress markers and intra-extracellular antioxidant activities in patients with endometriosis.

OBJECTIVE: The aim of the study is to evaluate alterations in intracellular and extracellular antioxidant enzymes activities and serum oxidative stress markers in patients with endometriosis. STUDY DESIGN: The current prospective study consisted of 31 female patients with endometriosis and 27 healthy controls. Serum total thiol, native thiol, disulphide, catalase, myeloperoxidase, and ceruloplasmin concentrations were measured. Laboratory and clinical data of all participants were recorded to compare the differences between the study and the control groups. RESULTS: Serum native thiol and total thiol levels in the study group were significantly lower than those in the control group [(p=0.009, p=0.03, respectively)]. Serum catalase levels are significantly higher in patients with endometriosis comparing to the control group (p=0.009). CONCLUSIONS: The finding that significant differences in serum total thiol, native thiol, and catalase levels observed in endometriotic patients supports that oxidative stress carries weigh in the pathophysiological aspects of endometriosis. Also significantly low levels of extracellular antioxidants and significantly high levels of intracellular antioxidants in endometriotic patients may arise from differences of free radicals in endometriosis and the activity levels of endometriosis. These non-invasive serum markers might give us an opportunity to monitor the disease's progress during the treatment.