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Home > Journal of Shalamar Medical and Dental College > Volume 3 Issue 1 of Journal of Shalamar Medical and Dental College

Glucose Insulin Ratio in Hyper Insulinemic Women with Polycystic Ovarian Syndrome |
Journal of Shalamar Medical and Dental College
Journal of Shalamar Medical and Dental College

Article Info
Authors

Volume

3

Issue

1

Year

2022

ARI Id

1682060070609_2980

Pages

101-105

DOI

10.53685/jshmdc.v3i1.98

PDF URL

https://journal.smdc.edu.pk/index.php/journal/article/download/98/57

Chapter URL

https://journal.smdc.edu.pk/index.php/journal/article/view/98

Subjects

Hyperinsulinemia glucose insulin ratio PCOS women

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INTRODUCTION

Polycystic ovarian syndrome (PCOS) is a prevalent metabolic disorder, triggered by interaction of genetic and environmental factors. PCOS may be caused by decreased insulin sensitivity in insulin sensitive tissues especially skeletal muscles that in turn increases the risk of developing metabolic syndrome.1

Polycystic ovarian syndrome is linked with metabolic disorders and failure of hypothalamic pituitary ovarian axis results in insulin resistance (IR) and consequently hyperinsulinemia. Hyperinsulinemia leads to increased androgen levels resulting in infertility, endometrial dysfunction, and obesity.2,3

Coexistence of obesity and PCOS may hamper weight loss in these individuals and further worsen their reproductive problems.4,5,6 Approximately 70% of the women with PCOS have high IR associated with impaired glucose metabolism in fat tissue.7 In PCOS decreased expression of GLUT4 may impair insulin mediated uptake of glucose and consequent hyperinsulenemia.8,9

 

Fasting glucose: insulin ratio (G/I ratio) is a reliable laboratory investigation compared with conventional investigations, to predict insulin sensitivity in women with PCOS. Women with a reduced G/I ratio (< 7.0) had higher BMI and higher fasting circulating insulin.10

Women with PCOS are highly resistant to insulin, and the ensuing hyperinsulinemia worsens the gynecological issues.11 The criteria for finding the insulin sensitivity is the technique of clamp of hyper insulinemic- euglycemic part. Though, this method is expensive and difficult and not carried out in routine. Other methods, like HOMA IR, and

G/I ratio are simple and easy to be carried out.12

Identifying the women with PCOS having IR may be helpful in starting the right treatment. Present study was designed to assess the role of G/I ratio as a potential biomarker for the hyper insulinemia in women with polycystic ovarian syndrome.

MATERIALS AND METHODS

A cross sectional comparative study was conducted at Lahore General Hospital after taking approval from institutional review board. Sample size was calculated by Raosoft Survey software tools. PCOS was diagnosed using the Rotterdam criteria.13 Non probability convenient sampling technique was used.

A total of 80 women 24-35 years of age were recruited from Obstetrics and Gynecology department of Lahore General Hospital after taking consent. 50 women had PCOS and 30 were age matched healthy controls. The healthy women had regular menstruation, no signs of hypogonadism, and normal fasting blood glucose levels.

Women with other endocrinopathies, age >50 years, diabetes mellitus, cardiovascular problems, liver dysfunction, hypertension and taking anti-obesity or anti-diabetic drugs were excluded from the study.

Data was collected on a questionnaire designed for this study. Body weight, height and waist circumference were measured.

IR was defined as G/I ratio < 7.0 and BMI

≥25.0 kg/m2 was considered as overweight. Waist circumference was also measured. 5ml of venous blood was drawn after an overnight fast of 8-12 hours for estimation of blood glucose and insulin. Sample was immediately centrifuged and aliquoted. Blood glucose was estimated immediately by glucose oxidase method and serum insulin was determined by

ELISA. IR was calculated by HOMA-IR method and index of insulin sensitivity was

 

Table 2: Biochemical parameters of women with and without PCOS

derived from G/I ratio.14 β-cell function was

Variables PCOS

Shape6 n=50

Control

n=30

assessed by HOMA- β.15

 

Statistical Analysis

Data was analyzed by SPSS version 24.

 

Fasting blood Glucose (mg/dl)

Fasting serum Insulin (IU/ml)

mean ±SD mean ±SD p-value

Shape7 119.1 ±14.9 94.1 ± 8.5 0.41

 

33.8 ± 15.8 3.4 ± 2.6 0.001

Variables were presented as mean±SD. Comparison of variables between study groups was done by student' t ' test. p<0.05 was considered statistically significant.

 

RESULTS

BMI of the women with PCOS was higher than healthy controls but this difference was not significant statistically (p=0.40). Waist circumference of the women with PCOS was also higher than healthy controls but this difference was not significant statistically (p=0.41) as shown in (Table 1).

 

Table 1: Baseline characteristics of the women with and without PCOS

Variables

PCOS n=50

Controls n=30

 

 

mean±SD

mean±SD

p-value

Age (years)

29.89±3.54

28.6±1.1

0.55

BMI

(Kg/m2)

 

29.8 ± 4.4

 

24.6 ± 1.8

 

0.40

Waist (inches)

 

29.8±1.9

 

24.4±2.9

 

0.41

"t" test was applied, p value<0.05 was considered

statistically significant

 

Fasting blood glucose, fasting insulin, HOMA-β and HOMA-IR were significantly higher in PCOS group compared to healthy controls (p<0.001). Glucose insulin ratio was lower in PCOS group compared to healthy controls (Standard value of Glucose Insulin ratio is >4.5) (Table 2).

G/I 3.52 28.48 -

HOMA-IR 4.46 ± 2.7* 0.44 ± 0.6 0.001

HOMA-β 155.80 49.40 -

Shape8

"t" test was applied, p value<0.05 was considered statistically significant

 

 

DISCUSSION

Mean age of women with PCOS was 28 to 29 years. Previous studies report that the prevalence of PCOS is 17.23% in women aged between 21-30 years.16 High prevalence of PCOS in women aged 21-30 years is due to increased activity of reproductive hormones that exert stimulatory effects on ovary and gradually decrease with age.17 It is also believed that impaired hypothalamic-pituitary- ovarian axis, high levels of serum insulin, IR, and impaired function of adrenal gland may cause PCOS.18, 19

We observed that BMI and waist circumference of women with PCOS were non-significantly higher as compared to controls. A study was carried out in 66 Indian women with PCOS 20-31 years of age. Study suggested that waist-to-hip ratio and BMI may predict IR in women with PCOS. Study also stated that waist-hip ratio is better predictor of insulin resistance and PCOS than BMI.20 Another study was carried out in 61 PCOS women of Ireland. Study stated that some cardio-metabolic irregularities in PCOS are associated with central obesity.21Another study stated the waist circumference reflects the visceral fat, which can forecast the beginning of IR.22

Fasting glucose, fasting insulin, HOMA-IR and HOM A -β were high in women

with

PCOS as compared to healthy controls. G/I ratio is less in women with PCOS as compared to healthy controls.

Literature reveals that in women with PCOS, there is a noteworthy decrease in uptake of glucose. BMI affects the functioning of β-cells causes IR in women with PCOS. 23,24

Fasting hyper-insulinemia indicates IR. Basal and glucose-induced hyperinsulinemia are observed in obese women with PCOS and it is secondary to intense insulin resistance. Higher fasting blood glucose in obese women with PCOS is secondary to raised hepatic glucose production and increased insulin resistance. Some studies report that hyperinsulinemia seems to induce excessive production of androgens and augments the effect of the luteinizing hormone (LH) in women with PCOS.25

G:I ratio can be a good indicator of insulin sensitivity in obese women with PCOS and has both specificity and high sensitivity for finding IR in PCOS women. The resultant hyperinsulinemia may have a role in reproductive irregularities of women with PCOS. It is proposed that ratio of glucose to insulin could be additional parameter to assess insulin resistance.

CONCLUSION

In addition to HOMA-IR, glucose insulin ratio may be considered to assess hyperinsulinemia and IR in women with polycystic ovarian syndrome.

Conflicts of interest

All authors declared no conflict of interest.

Contributors

RJ: Initial idea and writing of manuscript

MH: Contributed to the literature search and discussion

ST: Contributed to the literature search and discussion

SS: Data Collection and proofreading

TK: Entered the data and performed statistical

Analysis

SR: Revised the manuscript for intellectual content

All authors approved the final version and signed the agreement to be accountable for all aspects of work.

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