Morphological analysis of the rectus abdominis muscle in pregnant women with hyperglycemia and urinary incontinence

Rudge M V C1, Vesentini G1, Piculo F2, Harada B S1, Leite A P S1, Fernandes J N1, Pinto C G3, Damasceno D C1, Matheus S M M3, Barneze S1, Barbosa A M P4, Marini G5

Research Type

Pure and Applied Science / Translational

Abstract Category

Anatomy / Biomechanics

Abstract 559
Open Discussion ePosters
Scientific Open Discussion Session 28
Friday 31st August 2018
13:15 - 13:20 (ePoster Station 7)
Exhibition Hall
Anatomy Biomechanics Female Incontinence
1. UNESP/ Faculdade de Medicina de Botucatu, SP, Brasil, 2. Faculdades Integradas de Bauru, Bauru, SP, Brasil, 3. UNESP/ Instituto de Biociência de Botucatu, SP, Brasil, 4. UNESP/ Faculdade de Filosofia e Ciências, Marília, SP, Brasil, 5. . UNESP/ Faculdade de Medicina de Botucatu, SP, Brasil
Presenter
Links

Poster

Abstract

Hypothesis / aims of study
The American Diabetes Society estimates that 1 in 5 pregnant women (18%) are at risk of having gestational diabetes mellitus [1] and the prevalence of urinary incontinence (UI) during pregnancy may reach 75%. Skeletal striated muscle is the main organ of glucose metabolism, so it is of great importance to study the muscular changes due to gestational hyperglycemia.The aim of this study was to analyze the morphology of fiber types and extracellular matrix in the rectus abdominis muscle of pregnant women with hyperglycemia and urinary incontinence
Study design, materials and methods
Were included pregnant women who underwent prenatal care and underwent cesarean delivery in the aforementioned Department, without previous diagnosis of diabetes and hyperglycemia, without previous UI, with current gestational UI and agreed to sign the informed consent form. The incontinent women were divided into two groups: hyperglycemic pregnant women and normoglycemic pregnant women. During the surgical procedure of the cesarean section, a sample of the rectus abdominis muscle was removed with 1cm in diameter and the tissues were intended histological analysis with hematoxylin-eosin and picrossíruis red and immunohistochemistry for fast and slow fibers.
Results
Of the 324 women who accepted to participate in the study, 250 or evolved to normal deliveries or out-of-service deliveries, 74 biopsies were performed but after 37 losses in the processing of the material, the final analysis of the rectus abdominis muscle was performed in 21 women in the hyperglycemic group and 16 in the normoglycemic group. The groups were homogeneous in all sociodemographic and clinical variables, except for the glycemic average and values of the oral glucose tolerance test. In the morphometric variables, the hyperglycemic group had a smaller area and diameter of the slow fibers when compared to the normoglycemic group (p = 0.0241 and p = 0.0019 respectively), besides the loss of predominance of fast fibers. There was no difference in relation to the area , diameter and number of fast fibers, number of slow fibers and amount of collagen. (Table 1)
Interpretation of results
It is known that diabetes induces functional, metabolic and structural changes in skeletal muscle and the morphological changes found in this work are in agreement with the results found in animal models in the urethral and rectus abdominis muscle of diabetic pregnant rats, which demonstrate the loss of predominantly fast fiber [2,3]
Concluding message
Hyperglycemia leads to changes in the fibers of the rectus abdominis muscle in pregnant women with urinary incontinence. This study is the beginning of a line research that confirms in humans the same alterations found in animal models and requires future investigations.
Figure 1
References
  1. Biopsy
  2. Hyperglycemia
  3. Rectus abdominis
Disclosures
Funding #2013/26214-7and 2016/09710-9 , São Paulo Research Foundation (FAPESP)/Brazil. Clinical Trial No Subjects Human Ethics Committee Research Ethics Committee of Botucatu Medical School - UNESP (CAAE 41570815.0.0000.5411 no. 986.465). Helsinki Yes Informed Consent Yes
20/11/2024 11:07:56