Analysis of D-Chiro inositol in lowering androgen levels in PCOS patients


 Background and objectives: Polycystic ovarian syndrome (PCOS) involves dysfunction in the endocrinal, metabolic and reproductive profile among females. D-chiro inositol is a novel treatment agent for improving the endocrinal profile seen in it. The current study aims to evaluate the effect of D-Chiro Inositol in lowering down the androgens levels in patients with PCOS. Methodology of the study: This randomized trial was carried out at the outpatient of Department of medical sciences during June 2020 to March 2021. 50 females with polycystic ovarian disease were divided randomly into two groups, each of 25 females. One group was give D-Chiro Inositol (600mg/day) and the other was given placebo. Androgens levels i.e. LH, FSH and testosterone were assessed at baseline and then after 8 weeks. Treatment effects were compared after 8 weeks by independent sample T test and a P value of ≤0.05 was considered significant. Results: The mean age of the patients in the treatment (D-Chiro Inositol) group was 28±8 year’s vs 30±9 years in placebo group. The mean BMI of females in D-Chiro Inositol group was 25.7±3.6 kg/m2 compared to 25.8±4.2 kg/m2 in the placebo group. The mean levels of LH, FSH and testosterone were 14.74 mIU/ml, 10.19 mIU/ml and 78.48 ng/dL in D-Chiro Inositol group vs 17.22 mIU/ml, 13.03 mIU/ml and 86.08 g/dl in placebo group. Significant difference was present between both treatment groups (P value ≤0.05). Conclusion: D-Chiro Inositol is a promising drug for the lowering down the androgens levels in polycystic ovarian syndrome.

Pakistan is lacking regarding the e cacy of this evolving drug. So the aim of current research is to evaluate the effect of D-Chiro Inositol in lowering down androgens levels in female patients with PCOS.
This will help in raising awareness among treating physicians regarding this new therapy that can help in reducing morbidity associated with this condition.

Methodology:
This randomized trial was carried out at the outpatient of Department of medical Sciences during June 2020 to March 2021. Total 50 females, between 18-45 years of age, who ful lled the de nition of polycystic ovarian syndrome i.e. having 2 out of these 3 features such as hyperandrogenism (evident clinically by hirsutism), anovulation and presence of polycystic ovaries on ultrasound, were registered in the research after obtaining informed consent and seeking hospital ethical committee approval. Patients who were already taking medications previously for polycystic ovarian syndrome were excluded as well as patients with hypothyroidism and with raised prolactin levels.
After noting down the demographic details of the patients, baseline levels of LH, FSH and testosterone were measured and recorded. The participants that were eligible were designated randomly to 1 of the 2 groups of treatment in equal proportion (25 females in each group) for 8 weeks: one group was given D-Chiro Inositol alone (600 mg/day) and the other was given placebo alone. The randomization of participants was done through a table generated by a computer so that in each group the numbers of participants could be approximately equalized. Assignment of patients into groups was done after completion of all screening assessments. To make concealment of the assigned treatment certain, a research pharmacist carried out randomization without the investigator, who did it at another center and provided the medications in containers that were coded and had similarly looking capsules of D-Chiro Inositol or placebo handed over by the manufacturer. Placebo was a B-complex vitamin, which was considered to have no effect on androgen levels. After completion of 8 weeks, serum levels of LH, FSH and testosterone were again assessed and compared with the levels at baseline and were subjected to analysis statistically.
Data was analyzed using SPSS version 17.0. Quantitative data such as age, body mass index, LH, FSH and testosterone was assessed as mean and standard deviation. Qualitative data such as obesity, presence of diabetes was assessed as frequency and percentages. Data was strati ed for age, obesity and presence of diabetes. Post strati cation Chi square test was applied to deal with the effect modi ers and a P value of ≤0.05 was considered signi cant. Independent sample T-test was applied to compare the effects of both treatment. A p value of ≤0.05 was considered signi cant.

Results:
A total of 50 female patients with Polycystic Ovarian Disease were assessed. The mean age of the patients in the treatment (D-Chiro Inositol) group was 28 years with a standard deviation of 8 and mean age in the placebo group was 30 years with standard deviation of 9. The mean body mass index of females in D-Chiro Inositol group was 25.7±3.6 kg/m 2 compared to 25.8±4.2 kg/m 2 in the placebo group. The mean LH, FSH and testosterone levels were 18.6 mIU/ml, 13.59 mIU/ml and 90.7ng/dl at baseline in the treatment group respectively. The mean LH, FSH and testosterone levels were 17.72mIU/ml, 13.6mIU/ml, and 89.04 ng/dl at baseline in the placebo group respectively. Among 25 female patients who were treated With D-Chiro Inositol, 11 (44%) had obesity and 5 (20%) had diabetes, whereas among 25 female patients who received placebo, 10 (40%) had obesity and 4 (16%) had diabetes. The mean levels of LH, FSH and testosterone were 14.74 mIU/ml, 10.19 mIU/ml and 78.48 ng/dL in D-Chiro Inositol group vs 17.22 mIU/ml, 13.03 mIU/ml and 86.08 g/dl in placebo group after 8 weeks.
Independent sample T-test was applied to look for the difference between the two groups. The results revealed that the group which received D-Chiro Inositol showed signi cant reduction in the levels of androgens i.e. LH, FSH and Testosterone as indicated by a P-value of ≤0.05 and the independent sample T test revealed that treatment with D-Chiro Inositol was signi cantly better compared to placebo in lowering down the levels of androgens (P value ≤0.05).
Strati cation of data was done for age, obesity and presence of diabetes. Chi square test was applied after strati cation to see the impact of these modi ers and it was found that none of these factors had any signi cant impact on the treatment outcome. In 2015, Antonio Simone Lagana conducted a study and evaluated the effect of DCI on functions of ovaries and metabolism in females having polycystic ovarian syndrome 2 . The patients were given DCI in a dose of 1 gram per day along with folic acid 400 mcg per day orally for a period of 6 months. The authors assessed the effect of treatment on body mass index, blood pressure (both systolic and diastolic), serum LH, FSH, free and total testosterone, androstenedione and prolactin levels and also assessed the impact of treatment on menstrual regularity. The results revealed that D-Chiro Inositol resulted in signi cantly lower systolic blood pressure, LH levels, FSH, free and total testosterone levels, decrease androstenedione and prolactin amount 2 . They also found that regularization of menstrual cycle after treatment was signi cant statistically too. The current research result also yielded similar effect of treatment with D-Chiro Inositol on LH, FSH and testosterone. However, the current study did not evaluate the effect on other endocrinal parameters or did not see the effect on blood pressure or regularity of menstrual cycle. So further studies in this context should be carried out.

Conclusion:
In conclusion, treatment of polycystic ovarian syndrome with D-Chiro Inositol is effective. It is a promising therapy in patients with PCOS and results in an improved hormonal pro le. Despite the current study data, there is still a further need of evaluating larger samples and carrying out studies with more statistical power so that the outcomes after treating with d-chiro inositol can be clari ed.

Declarations
Competing interests: The authors declare no competing interests.