Background: Many previous studies were concerned with
the relationship between gestational diabetes and the
development of vaginal candidiasis in pregnant women. In
this study, our aim is directed to uncover glucose tolerance
status in non-diabetic pregnant women inflicted with
candida albicans.
Methods: Thirty-four pregnant women with vaginal
condidiasis (as demonstrated by microscopy) were enrolled
in this study. The patients were nearly similar in their
anthropometric and demographic criteria with those of the
healthy pregnant women (control group, forty –two
women). Fasting plasma sugar and glucose tolerance test
were alone for all patients and control group.
Results: fasting plasma sugar was significantly higher in
the candidiasis-positive pregnant women in comparison to
those of candidiasis-negative subjects (5.09 mmol/L vs.
4.71, p <0.02). Plasma glucose level after 30 minutes of
performing oral glucose tolerance test was also significant
(8.47mmol/Lvs. 7.84, P <0.04). The same trend of
significance was noticed after 60 minutes and 120 minutes
of performing the corresponding test.
The results were (8.13 mmol/L vs. 7.10, P <0.02) and
(6.90mmol/L vs. 6.15, P<0.05) respectively.
Conclusion: the results reveal an impaired oral glucose
tolerance test in pregnant women with candida albicans
POSSIBILITY OF APPLICATION THE BALANCED SCORECARD IN THE IRAQI INDUSTRIAL COMPANIES: A PROPOSED MODEL
LO Hamza, Indian Journal of Natural Sciences, 2018 - Cited by 3
The study aimed to investigate the role of Dectin-1 and Card-9 in pathogenicity of inflammatory bowel disease (IBD). This investigations involved 150 blood samples for IBD patients which divided in to two groups (50 for crohns disease CD (G2) and 50 for ulcerative colitis UC (G3)). All a apparently (male and female) attended to) Al-Kindy hospital) in Baghdad city, department of Gastroenterology. and all of thin were diagnosis by consulters medical staff and pathologists with age range 15-65years average 40 years. in addition to 50 blood samples were collected from apparently healthy individuals as control group (G1). 10 ml were withdrawn from all participants, 5ml for the immunological study which carried by ELISA technique and 5 ml used fo
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