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Is polymorphism of the STK11 gene a predictor of response to metformin in polycystic ovarian syndrome?
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Objectives: To evaluate possible associations between the genetic
polymorphism of the STK 11 gene and response to metformin in women with
polycystic ovary syndrome. Methods: This is a prospective longitudinal
cohort study of 57 women with polycystic ovary syndrome. Baseline
documentation of anthropometric measurements, menstrual history,
hirsutism, hair loss, acne, and biochemical parameters, in addition to
gene testing for STK11 polymorphism, were performed. Follow-up was
arranged at 6 cycles following oral metformin therapy, 850 mg, twice
daily. Results: Post-metformin therapy, there were statistically
significant improvements in menstrual frequency, blood loss, acne,
ultrasound findings, and a decrease in BMI, acne and hirsutism, but not
in alopecia. Fasting insulin decreased significantly, but fasting blood
sugar did not. Regarding Intron1 polymorphism, there was a significant
response in the CC subgroup in menstrual regularity and blood loss. The
CG subgroup showed a significant response in menstrual regularity and
ultrasound findings. The GG subgroup showed a significant response in
menstrual regularity, menstrual loss, acne and alopecia. Regarding
Intron 6 polymorphism, there was a significant response in the CC
subgroup in relation to menstrual regularity, blood loss, acne and
ultrasound findings. The CT subgroup showed a significant response in
menstrual regularity and ultrasound findings. The TT subgroup showed a
significant response only in relation to alopecia. Conclusion:
Polymorphism in STK11 is not predictive of response to metformin therapy
at a dose of 850 mg, twice daily.
Title: Is polymorphism of the STK11 gene a predictor of response to metformin in polycystic ovarian syndrome?
Description:
Objectives: To evaluate possible associations between the genetic
polymorphism of the STK 11 gene and response to metformin in women with
polycystic ovary syndrome.
Methods: This is a prospective longitudinal
cohort study of 57 women with polycystic ovary syndrome.
Baseline
documentation of anthropometric measurements, menstrual history,
hirsutism, hair loss, acne, and biochemical parameters, in addition to
gene testing for STK11 polymorphism, were performed.
Follow-up was
arranged at 6 cycles following oral metformin therapy, 850 mg, twice
daily.
Results: Post-metformin therapy, there were statistically
significant improvements in menstrual frequency, blood loss, acne,
ultrasound findings, and a decrease in BMI, acne and hirsutism, but not
in alopecia.
Fasting insulin decreased significantly, but fasting blood
sugar did not.
Regarding Intron1 polymorphism, there was a significant
response in the CC subgroup in menstrual regularity and blood loss.
The
CG subgroup showed a significant response in menstrual regularity and
ultrasound findings.
The GG subgroup showed a significant response in
menstrual regularity, menstrual loss, acne and alopecia.
Regarding
Intron 6 polymorphism, there was a significant response in the CC
subgroup in relation to menstrual regularity, blood loss, acne and
ultrasound findings.
The CT subgroup showed a significant response in
menstrual regularity and ultrasound findings.
The TT subgroup showed a
significant response only in relation to alopecia.
Conclusion:
Polymorphism in STK11 is not predictive of response to metformin therapy
at a dose of 850 mg, twice daily.
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