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Obstetrics & Gynecology International Journal

Research Article Volume 6 Issue 1

Study of Role of Metformin in Management of Polycystic Ovarian Syndrome

Suresh Chandra Mandal, Sandip Lahiri, Pinaki Sarkar

Department of Obstetrics & Gynaecology, West Bengal Health University, India

Correspondence: Suresh Mondal, Malda Medical College and Hospital, West Bengal Health University, Malda West Bengal, India, Tel 9734910276

Received: March 05, 2016 | Published: January 10, 2017

Citation: Mandal SC, Lahiri S, Radhika B, Sarkar P (2017) Study of Role of Metformin in Management of Polycystic Ovarian Syndrome. Obstet GynecolInt J 6(1): 00190. DOI: 10.15406/ogij.2017.06.00190

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Abstract

Background: Insulin resistance is a common feature of Polycystic Ovarian Syndrome and is present in approximately 40-50% of this disorder. Response to insulin sensitisers appear to be maximal in women with disturbed insulin sensitivity. This argues in favour of its usefulness in patients with marked hyperandrogenism and insulin resistance. In this study, only metformin is used as an insulin sensitising drug.

Methods: The study analysed the usefulness of short term metformin therapy to reduce features of hyperandrogenism and hyperinsulinemia in PCOS patients. Out of 96 patients of PCOS, 48 cases were treated with metformin (1500 mg / day) for 3 months to 1 year and 48 controls were advised dietary modification and exercise. The changes in weight, BMI, menstrual cycles, ovulatory response and hormonal changes were compared in case and control.

Results: Study reveals marked improvements in all parameters amongst the cases who received metformin therapy.

Conclusion: Metformin may be a highly effective treatment protocol for the improvement of clinical, biochemical and hormonal profile in PCOS.

Keywords: Polycystic ovary, Metformin, Hyperinsulinemia, Hyperandrogenism

Introduction

Polycystic Ovarian Syndrome is a heterogeneous disorder affecting 5-10% of women of reproductive age. Insulin resistance plays an important role in dysregulation of folliculogenesis, anovulation and hyperandrogenemia in this disorder. Given the central role of insulin in the aetiology of PCOS, insulin sensitising agents have the potential to ameliorate insulin resistance and alleviate the spectrum of endocrine, meatabolic and reproductive abnormalities in women with PCOS.

Metformin, an insulin sensitising drug was given to PCOS patients for 3 months to one year with an aim to achieve the following

  1. To decrease body weight and body mass index
  2. To decrease the features of hyperandrogenism like decreased hair loss, diminished facial and body hair growth
  3. Resumption of regular menstrual cycles
  4. To achieve ovulation and pregnancy in infertile patients; to reduce fasting insulin and testosterone levels
  5. To reduce LH, FSH and LH: FSH to normal level.

Material and methods

The prospective study was carried out in Malda Medical College and hospital from 1st July 2014 to 31st May 201. 96 patients with menstrual irregularities, ultrasound finding of polycystic ovaries and anovulation on folliculometry along with raised or altered LH, LH: FSH, insulin, testosterone levels were selected for the study. 48 cases received metformin (1500 mg/ day) for 3 months to 1 year depending on the response. The changes in weight, BMI, menstrual cycles, ovulatory response, and hormonal changes were critically analysed. These results were compared with rest 48 control patients of the same weight and BMI range who were advised dietary modification and exercise and the efficacy of metformin was assessed.

Result

Tables 1-4


Menstrual disorder

Total number

Cycle restored

Cycle not restored

Hypomenorrhoea

Case

4

4

100%

_

_

Control

4

2

50%

2

50%

Oligomenorrhoea
( 35 d- 3 months)

Case

30

22

73.3%

8

26.7%

Control

30

10

33.3%

20

66.7%

Oligomenorrhoea
(3mths- 6mths)

Case

14

10

71.4%

4

28.6%

Control

10

2

20%

8

80%

Amenorrhoea

Case

0

0

0

0

0

Control

4

0

0

4

100%

Total

 

 

36

75%

12

25%

 

 

14

29.2%

34

70.8%

Table 1 Change in menstrual disorder after treatment between cases and control


Effect

Case

Control

No Hirsutism

Hirsutism

No Hirsutism

Hirsutism

Before Treatment

38

79.2%

10

20.8%

38

79.2%

10

20.8%

After
Treatment

38

79.2%

10

20.8%

38

79.2%

10

20.8%

Table 2 Effect on Hirsutism on treatment in case & control


Mean

Case ( 48 )

Control ( 48 )

parameters

Before treatment

After treatment

Before treatment

After treatment

Wt ( kg )

53.29

51.86

53.17

52.63

BMI ( kg/ m2)

23.01

22.36

23.05

23.66

LH ( mIu/ ml )

19.63

7.34

14.01

13.59

LH:FSH

2.32:1

1.07:1

2.09:1

2.19:1

Fasting insulin (mIU/ml )

12.48

7.33

10.35

10.51

Testosterone

0.68

0.54

0.63

0.64

Table 3 Evaluation of changes in mean values in different parameters amongst case & control before and after treatment


Duration of ovulation

Total

Ovulation

Anovulation

3 Months to 6 Months

24

16

66.7%

8

33.3%

3-6 Months with Clomiphene

4

4

100%

_

_

6 Months to 12 Months

18

14

77.8%

4

22.2%

6 -12 Months with Clomiphene

2

2

100%

_

_

Table 4 Response of Metformin on ovulation

Discussion

75% cases in our study showed cycle restoration in contrast to 29.2% in control. Marked improvements in all parameters like weight, BMI, LH, LH: FSH, fasting insulin, and testosterone were found in cases who received metformin therapy. Metformin could not show any improvement in hirsutism score. 36 (75%) out of 48 cases became ovulatory with metformin treatment. 6 of them needed additional clomiphene. 16 (44.4%) cases ovulated with 3-6 months of metformin and 14 (38.9%) needed them for 6-12 months.

Conclusion

Metformin either by weight reduction or by modest reduction of insulin and androgen level helps in restoration of menstrual cycles, ovulation and normalise LH: FSH, insulin and testosterone level as evident in our study. Metformin has also been found to potentiate the action of ovulation inducing drugs. Metformin may be considered as a useful drug reserved for infertile PCOS patients who are not responding to clomiphene citrate.

Acknowledgments

None.

Conflicts of interest

None.

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