BackgroundApart from endoscopic interventions, readily attainable cost-effective biomarkers for ulcerative colitis (UC) assessment are required. For this purpose, we evaluated differential leucocytic ratio, mainly neutrophil–lymphocyte ratio (NLR) and lymphocyte-monocyte ratio (LMR) as simple available indicators of disease activity in patients with ulcerative colitis.MethodsStudy conducted on 80 UC patients who were classified into two groups of 40 each according to Mayo score and colonoscopic findings. Group 1 (active UC) and group 2 (inactive UC). Another 40 group-matched healthy participants were enrolled. White blood cell count, NLR, LMR, C-reactive protein, and Erythrocyte sedimentation rate were measured and recorded.ResultsSignificant elevation of NLR was observed in active UC group compared to inactive UC and controls (2.63 ± 0.43, 1.64 ± 0.25, 1.44 ± 0.19 respectively; p < 0.0001). The optimal NLR cut-off value for active UC was > 1.91, with a sensitivity and a specificity of 90% and 90% respectively. The mean LMRs of active UC was significantly lower compared with inactive UC patients and controls (2.25 ± 0.51, 3.58 ± 0.76, 3.64 ± 0.49 respectively; p < 0.0001). The cut-off value of LMR for determining the disease activity was ≤ 2.88 with a sensitivity of 90% and a specificity of 90%. NLR, LMR, and CRP were found to be significant independent markers for discriminating disease activity (p = 0.000). Besides, NLR was significantly higher in patients with pancolitis and positively correlated with endoscopically severe disease.ConclusionNLRs and LMRs are simple non-invasive affordable independent markers of disease activity in UC.
Studies proposed a link between gut microbiota and airway tract. Study the diversity and density of gut microbiota in healthy and asthmatic patients. Semi-quantitative stool cultures were performed from fecal samples collected from 80 adult asthmatic patients and 40 healthy individuals. Data on gender, age, dietetic history, clinical examination and investigations as skin prick test and pulmonary function testing were also collected. were found to be higher among patient group than control group. density was statistically higher in patient than control group. No significant difference was detected between male and female patients or controls. were statistically more prevalent in stool culture of male cases than that of male controls. No difference was found between female cases and controls. There was no relationship between type of microbial growth and disease related parameters including age, duration of illness, number of allergens and pulmonary function test in cases. Atopic asthma is significantly associated with gut microbiota and. It is important to determine the organism involved, to focus on microbiome-driven disease and therapies.
The majority of patients from Egypt had uncontrolled hypertension even after receiving treatment. This might increase awareness among physicians and enable them to prescribe appropriate treatment to patients with uncontrolled BP. Key limitations: The questionnaire used in the study for the evaluation of patient/physician satisfaction level was not standardized and was based on the choice and practice of the physicians.
Background and Aims:
Women who develop GDM (gestational diabetes mellitus) have a
relative insulin secretion deficiency, the severity of which may be predictive for later development of
diabetes. This study aimed to investigate the role of fasting plasma glucagon in the prediction of later
development of diabetes in pregnant women with GDM.
Materials and Methods:
The study was conducted on 150 pregnant women with GDM after giving
informed oral and written consents and being approved by the research ethical committee according to
the declaration of Helsinki. The study was conducted in two phases, first phase during pregnancy and
the second one was 6 months post-partum, as we measured fasting plasma glucagon before and after
delivery together with fasting and 2 hour post-prandial plasma sugar.
Results:
Our findings suggested that glucagon levels significantly increased after delivery in the majority
14/25 (56%) of GDM women who developed type 2 DM within 6 months after delivery compared
to 6/20 (30%) patients with impaired fasting plasma glucose (IFG) and only 22/105 (20%) non
DM women, as the median glucagon levels were 80,76, 55, respectively. Also, there was a high statistical
difference between fasting plasma glucagon post-delivery among diabetic and non-diabetic
women (p ≤ 0.001). These results indicated the useful role of assessing fasting plasma glucagon before
and after delivery in patients with GDM to predict the possibility of type 2 DM.
Conclusion:
There is a relatively high glucagon level in GDM patients, which is a significant pathogenic
factor in the incidence of subsequent diabetes in women with a history of GDM. This could be
important in the design of follow-up programs for women with previous GDM.
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