Insulin Resistance Clinical Trial
Official title:
The Role of Insulin Resistance in Recurrent Miscarriage
The objective of this study is to study the association between insulin resistance and recurrent spontaneous miscarriage (RSM).
This a case-control study which was performed during the period from (December 2013) till
(June 2014). Researcher had 80 participants presented to the outpatient clinic in Ain Shams
University Maternity hospital; they were classified into two groups: (Group A) case group:
40 pregnant females at 6- 13wks presenting with a history of recurrent pregnancy loss (two
or more failed clinical pregnancies as documented by ultrasonography or histopathology
examination according to the American Society of Reproductive Medicine). (Group B) control
group: 40 pregnant females at 6- 13wks with no history of abortion. They were selected
according to inclusion and exclusion criteria:
- Inclusion criteria:
1. Women in the child bearing period between 23-40 years.
2. All patients were pregnant.
3. The gestational age of both groups 6-13 weeks(1st trimester)
- Exclusion criteria:
1. Patients with history of gestational diabetes.
2. The patients on medication that could affect glucose metabolism at the time of the
study (as metformin, Pioglitazone,rosiglitazone).
3. Patients with other causes of recurrent abortion as (thyroid dysfunction, uterine
anomalies, chromosomal abnormalities, antiphospholipid antibody syndrome).
4. Patients with PCOS in the control group (they have insulin resistance).
5. Obese patients (BMI >30).
The study was conducted after approval of the hospital ethical committee and a written
consent was taken from all cases and controls participating in the study after full
explanation. For all participants detailed history taking, full examination including body
mass index was taken. The subjects were asked to go on a normal diet for 3 days prior to
oral glucose tolerance test (OGTT). A fast for 8-10 h was required prior to sampling. A
venous blood sample was drawn on the following morning from each subject to determine the
concentrations of fasting glucose (FG) and fasting insulin (FI), afterwards subjects were
required to drink a mixture of 75 g of pure glucose in 250 ml of water, venous blood samples
were drawn again after 1, 2, and 3 h to determine the concentrations of glucose and insulin
blood samples for determination of fasting glucose and fasting insulin after 8-10hours
fasting and oral glucose tolerance test. Glucose concentration was determined using the
hexokinase endpoint method; while insulin concentration was determined using the
immunoluminescence method. The Immulite2000 Immunoassay Analyzer was used along with the
necessary reagents. The homeostasis model assessment of insulin resistance index (HOMA-IR)
for each subject was calculated as follows: [FI (U/ ml) ×FG (mmol/l)]/22.5.The larger the
HOMA-IR, the more severe the degree of IR. HOMA-B, which represents the endocrine function
of insulin, is calculated as 20× FI/ (FG-3.5). I 60 /I 0 represent the rate of 1-hour
insulin to 1-hour glucose, and I60 / G60 represent the rate of 1-hour insulin increase to
1-hour glucose increase. Both values reflect the endocrine functions of B cells of the
pancreatic gland. The area under the curve of glucose (AUCG) is equal to half of the FG plus
1-hour glucose, 2-hour glucose, and half of the 3-hour glucose. The area under the curve of
insulin (AUCI) is also computed in this manner for insulin. The ratio AUCI/AUCG represents
the rate of AUCI to AUCG, and the higher the rate, the more severe the degree of IR.
;
Observational Model: Case Control, Time Perspective: Cross-Sectional
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