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1.
Acta Diabetol ; 45(3): 157-65, 2008 Sep.
Article in English | MEDLINE | ID: mdl-18496643

ABSTRACT

Screening for glucose intolerance during pregnancy provides an opportunity to offer management to those women diagnosed with gestational diabetes mellitus. However, there is a need to diagnose gestational diabetes early to minimize exposure of the developing fetus to suboptimal conditions and prevent perinatal complications and their sequelae. The purpose of this study was to identify potential biomarkers for impending gestational diabetes that appear in the plasma before impaired glucose tolerance. Pregnant women were prospectively recruited to the study and blood was collected at the first antenatal visit and at the time of routine oral glucose tolerance test. Women diagnosed with gestational diabetes were matched with an equal number of normal pregnant (control) women. Biomarkers under investigation included endocrine and metabolic hormones, cytokines and chemokines, and surrogate markers of oxidative stress. Compared to controls, women with gestational diabetes exhibited elevated plasma insulin and reduced plasma adiponectin concentrations at 28 weeks gestation. Significant differences in insulin and adiponectin concentrations were also observed in plasma at 11 weeks gestation. Bivariate logistic regression analysis showed that both insulin and adiponectin are associated with subsequent development of gestational diabetes. Plasma insulin and adiponectin concentrations, when measured at 11 weeks, may be predictive of impending gestational diabetes. Further studies are warranted to determine the reliability of these biomarkers.


Subject(s)
Biomarkers/blood , Diabetes, Gestational/diagnosis , Mass Screening , Adipokines/blood , Adult , Biomarkers/analysis , Blood Glucose/analysis , Case-Control Studies , Chemokines/blood , Cytokines/blood , Diabetes, Gestational/blood , Female , Glucose Intolerance/blood , Glucose Intolerance/diagnosis , Glucose Tolerance Test , Humans , Insulin/blood , Insulin Resistance/physiology , Mass Screening/methods , Postpartum Period/blood , Pregnancy , Pregnancy Trimester, First/blood , Prognosis
2.
Aust N Z J Obstet Gynaecol ; 48(6): 536-41, 2008 Dec.
Article in English | MEDLINE | ID: mdl-19133039

ABSTRACT

AIM: Inherited thrombophilic polymorphisms have been linked to pregnancy-related thromboembolism and other adverse pregnancy outcomes. As there are limited data on the prevalence of these polymorphisms in Australian populations, we aimed to assess this in an antenatal population. METHODS: Healthy nulliparous women (n = 2031) were recruited to this study. The women had no past or family history of venous thromboembolism. Women were excluded if they or a family member was known to be a carrier of any thrombophilic marker. Genotyping from venous blood for the factor V Leiden, prothrombin 20210A, MTHFR 677 and 1298 and thrombomodulin C1418T polymorphisms was undertaken. RESULTS: Key findings were that 107 of 2019 (5.30, 95% confidence interval 4.36-6.37%) women tested were heterozygous carriers of factor V Leiden and one was homozygous (0.05, 0-0.27%); 2.43% of women were heterozygous carriers of the prothrombin gene mutation (1.80-3.20%) while no women were homozygous for this mutation; 11.62% (10.22-13.02%) and 9.98% (8.67-11.29%) were homozygous for the MTHFR 677 and 1298 polymorphisms, respectively, and 3.43% (2.63-4.22%) of women were homozygous for the thrombomodulin polymorphism. CONCLUSIONS: The prevalence of these polymorphisms is consistent with previously published data in Caucasian populations. These data will provide the basis for further assessment of the relationship between poor pregnancy outcome and these inherited thrombophilic polymorphisms in an asymptomatic antenatal population.


Subject(s)
Blood Coagulation Disorders, Inherited/epidemiology , Factor V/genetics , Methylenetetrahydrofolate Reductase (NADPH2)/genetics , Polymorphism, Genetic , Prothrombin/genetics , Thrombomodulin/genetics , Thrombophilia/epidemiology , Australia/epidemiology , Blood Coagulation Disorders, Inherited/ethnology , Female , Gene Frequency , Genetic Predisposition to Disease , Heterozygote , Homozygote , Humans , Mutation , Pregnancy , Pregnancy Outcome/genetics , Prevalence , Thrombophilia/ethnology , Thrombophilia/genetics
3.
Aust N Z J Obstet Gynaecol ; 42(2): 125-9, 2002 May.
Article in English | MEDLINE | ID: mdl-12069137

ABSTRACT

METHODS: A questionnaire was administered to 958 women attending the antenatal clinic at Mercy Hospital for Women, Melbourne, to ascertain their choice of title during pregnancy Midwifery, nursing and medical staff (376 in total) were also invited to respond to a similar questionnaire. RESULTS: The response rate was 73.6% from the survey of all women who were overwhelmingly in favour of being called 'patient' as their first choice (34%), followed by 'other' (20%) and then 'mother' (19%). Virtually all women requesting 'other' wished to be called by their name. Women wishing to be called 'patient' for first choice did not significantly differ from the remainder of the study group in age, gestation, number of previous pregnancies, or number of children. When women from the Family Birth Centre (FBC) were analysed as a separate group, they had a clear preference to be called 'other' (unanimously, by their name) than the general antenatal population (odds ratio (OR) 5.1; 95% confidence interval (CI) 3.1, 8.3; p < 0.0001). The staff survey, with a response rate of 84%, also demonstrated that 'patient' was the most popular first choice for patient title. Medical staff were significantly more likely to choose 'patient' (OR 4.2, 95% CI 2.3, 7.7; p < 0.0001), though the term 'patient' was the preferred choice of all staff.


Subject(s)
Choice Behavior , Pregnancy/physiology , Terminology as Topic , Adult , Australia , Confidence Intervals , Female , Health Care Surveys , Humans , Infant, Newborn , Ireland , Labor, Obstetric , Odds Ratio , Patient Rights , Patient Satisfaction , Physician-Patient Relations , Postnatal Care/methods , Prenatal Care/methods , Probability , Professional-Patient Relations , Surveys and Questionnaires
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