Comparative Effects of Metformin and Insulin on Stereological Studies and Immunohistochemistry of Placenta
NCT ID: NCT04907708
Last Updated: 2021-06-01
Study Results
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Basic Information
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COMPLETED
NA
156 participants
INTERVENTIONAL
2018-01-01
2019-08-07
Brief Summary
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Detailed Description
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GDM produces anatomical and physiological alterations in placenta. This can be related to altered levels of fetal insulin and multiple growth factors such as placental vascular endothelial growth factor (VEGF), Insulin like growth factors (IGF and IGF binding proteins) which regulate the fetal and placental development. Morphologically, diabetic placentae are larger in size and volume. Microscopically, diabetic placenta shows degenerative alternations such as villous fibrinoid necrosis, chorangiosis, villous immaturity, calcification and syncytial knots formation which show intense hypoxia of the placental tissues.
Nutritional therapy (diet control) is foremost important for achieving target glucose values during pregnancy but in uncontrolled cases pharmacological intervention is required. Parental Insulin is the traditional therapy in such circumstances, but is an expensive medication and is associated with high incidence of neonatal and maternal hypoglycemia, still births, neonatal morbidity and mortality. It is documented to produce many placental alterations such as immature villi, hemorrhages, edema, cystic changes and fibrinoid necrosis. It has been postulated that the reason behind all these hypoxic changes are the variation in the blood glucose level that occur in the maternal blood as sugar level suddenly dropped soon after Insulin injection and are at highest just before the next dose of Insulin.
The use of oral anti-diabetic medications such as Metformin in the management of gestational diabetes has increased over the past several years. Recent studies has established that Metformin can be a better option for GDM as it well controls glycemia (produces euglycemic) with good pregnancy outcomes. Metformin is an oral anti-diabetic drug from biguanide group; work by improving insulin sensitivity, reducing hepatic gluconeogenesis and also by increasing peripheral glucose uptake and utilization. It is now been upgraded to category B drug as is not associated with teratogenic effects. But what are the effects of Metformin on stereological morphometric study and immunochemistry of placental tissues were left to be evaluated. Stereology provides practical measurements and significant approach for obtaining quantitative estimates of small structures on histological slides. In placental tissue it is performed to obtain unbiased quantitative estimates of placental components that inform about development and also estimate of structural parameters that have direct influence on placental functional capacity. Immunohistochemistry or immunofluorescence of tissue sections also provide valuable insight to placental structure and protein expression with three-dimensional spatial information, including morphology that cannot be obtained on microscopy.
With this background knowledge, study was designed with the following objectives:
1. To evaluate the placental gross and microscopic changes in normal, diet control, Metformin and Insulin treated in newly enrolled GDM females
2. To evaluate stereological morphometric details of placenta in normal, diet control, Metformin and Insulin all enrolled females
3. To evaluate immunohistochemistry of placental tissues in normal, diet control, Metformin and Insulin in all enrolled females
4. To compare the placental morphology, stereology and immunohistochemistry with in the groups.
5. To evaluate the fetal and maternal outcome in normal, diet control, Metformin and Insulin treated gestational diabetics.
6. To correlate the placental morphology with the fetal and maternal outcome in Metformin and Insulin treated gestational diabetics
Conditions
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Study Design
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RANDOMIZED
PARALLEL
OTHER
NONE
Study Groups
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Normal healthy controls
females in second trimester with normal glucose levels
No interventions assigned to this group
Diet controlled
females in second trimester with blood sugar levels below 129mg/dl
No interventions assigned to this group
Metformin
females in second trimester with blood sugar levels above 130mg/dl treated with Metformin
Metformin
Euglycemic agent
Insulin
females in second trimester with blood sugar levels above 130mg/dl being treated with Insulin
Insulin
Hypoglycemic agent
Interventions
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Metformin
Euglycemic agent
Insulin
Hypoglycemic agent
Eligibility Criteria
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Inclusion Criteria
1. Patients who were diagnosed as GDM during second trimester screening for FBS and RBS, confirmed further by OGCT and OGTT.
2. GDM patients who signed the written informed consent.
3. GDM patients who were in ages between 18 years and 40 years and had no other comorbid such hypertension, CVD etc
4. Full term GDM patients with singleton pregnancy (37 weeks and above)
5. GDM patients whose placenta were preserved within 30-40 minutes of delivery.
Exclusion Criteria
1. GDM Patients with ages less than 18 or more than 40 years
2. GDM females with some co-morbid and complications (e.g. hypertension, CVD, diabetes type 1 or diabetes type 2 before gestation, abnormal Urea Creatinine Electrolyte (UCE) and Liver function test (LFTs).
3. GDM Patients who delivered pre-termed (\< 37 weeks of gestation) or post termed (\>42 weeks of gestation)
4. GDM patients with twin pregnancy.
5. GDM Patients if not preserved in the formalin properly within 30-40 minutes of delivery.
6. GDM females who were given combined (Metformin and insulin) therapy.
18 Years
40 Years
FEMALE
Yes
Sponsors
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University of Karachi
OTHER
Responsible Party
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Dr Rabia Arshad
Principal Investigator
Principal Investigators
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KAUSER AAMIR, Ph.D
Role: STUDY_DIRECTOR
BMSI, JPMC,KARACHI
Locations
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Jinnah Post Graduate Medical Centre
Karachi, Sindh, Pakistan
Countries
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References
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Liang HL, Ma SJ, Xiao YN, Tan HZ. Comparative efficacy and safety of oral antidiabetic drugs and insulin in treating gestational diabetes mellitus: An updated PRISMA-compliant network meta-analysis. Medicine (Baltimore). 2017 Sep;96(38):e7939. doi: 10.1097/MD.0000000000007939.
Related Links
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Belkacemi, L., Kjos, S., Nelson, D. M., \& Desai, M. (2013). Reduced apoptosis in term placentas from gestational diabetic pregnancies. Journal of Developmental Origins of Health and Disease, 4 (3), 256-265.
Casson, I. F., Clarke, C, A., Howard, C.V., McKendrick, O., Pennycook, S., Pharoah, P.O.D. (1997). Outcomes of pregnancy in insulin dependent diabetic women: results of a five-year population cohort study, British Medical Journal, 315, 275.
Other Identifiers
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UKarachi
Identifier Type: -
Identifier Source: org_study_id
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