PCOS in Bipolar Women on Valproate

Women taking valproate for bipolar disorder are at significantly increased risk of developing features of polycystic ovary syndrome, according to a published study of 230 female patients in the Systematic Treatment Enhancement Program for Bipolar Disorder (STEP-BD) trial.

Investigators reported finding new-onset oligomenorrhea with hyperandrogenism in 9 (10.5%) of 86 women treated with valproate (Biol. Psychiatry 2006;59:1078–86).

Only 2 (1.4%) of 144 women on lithium or an anticonvulsant other than valproate developed these symptoms of polycystic ovary syndrome (PCOS).

In all cases, oligomenorrhea began within a year of the patient's starting valproate use. The investigators calculated the relative risk as 7.5 for women with bipolar disorder using valproate as a mood stabilizer.

Dr. Hadine Joffe, the lead author, is director of endocrine studies in the perinatal and reproductive psychiatry clinical research program at Massachusetts General Hospital in Boston.

She and her colleagues recommended warning women of PCOS risk before starting them on valproate.

Further, women on valproate should be evaluated for PCOS if they develop menstrual irregularities with hyperandrogenic symptoms. Along with PCOS treatment, the investigators suggested that “it may also be appropriate to consider alternative mood stabilizers if PCOS features develop on valproate.”

In an address at a psychiatric symposium sponsored by the University of Arizona, Dr. Gary Sachs, senior author and principal investigator of STEP-BD, emphasized the need for vigilance during the first year a patient is on valproate.

“Before you start women on valproate, you absolutely have to warn them this is a risk,” Dr. Sachs, founder and director of the bipolar clinic and research program at Massachusetts General Hospital, told psychiatrists at the Santa Fe, N.M., symposium, which was also sponsored by the University of Texas Southwestern Medical Center at Dallas and the University of New Mexico.

Sponsored by the National Institute of Mental Health, STEP-BD enrolled 4,361 patients in the largest clinical study to date on the treatment of bipolar disorder. Dr. Sachs said that Abbott Laboratories, which sells valproate under the brand name Depakote, was among the drug companies that supported the trial.

“They were very confident the risk wasn't there,” he said. “It turned out that was wrong. There really was a risk. The risks are there and published.”

To study the relationship in a nonepileptic population, the investigators sought out women aged 18–45 years in STEP-BD who were taking at least one mood stabilizer for at least 3 months.

Participants who had discontinued another mood stabilizer within the previous 3 months were not included in the substudy.

Of the 300 identified eligible women, 14 patients previously diagnosed with PCOS and three others with disorders involving oligomenorrhea were among those excluded from the sample. All told, 230 women were available for the analysis.

Of the valproate users, 12 developed oligomenorrhea, and 9 of them also had hirsutism, according to the report.

Among all patients with oligomenorrhea, valproate users had fewer menstrual cycles (median of 5 vs. 8.5 per year) than did nonusers.

Some had elevated total or free testosterone, moderate to severe acne, or male-pattern alopecia.

The valproate users who developed oligomenorrhea with hyperandrogenism had a higher median body mass index (kg/m

“Our study raises the possibility that increased body weight, insulin resistance, PCO morphology, younger age of first valproate use, and polypharmacy may predispose to the development of PCOS features on valproate,” the investigators concluded.

Women taking valproate for bipolar disorder are at significantly increased risk of developing features of polycystic ovary syndrome, according to a published study of 230 female patients in the Systematic Treatment Enhancement Program for Bipolar Disorder (STEP-BD) trial.

Investigators reported finding new-onset oligomenorrhea with hyperandrogenism in 9 (10.5%) of 86 women treated with valproate (Biol. Psychiatry 2006;59:1078–86).

Only 2 (1.4%) of 144 women on lithium or an anticonvulsant other than valproate developed these symptoms of polycystic ovary syndrome (PCOS).

In all cases, oligomenorrhea began within a year of the patient's starting valproate use. The investigators calculated the relative risk as 7.5 for women with bipolar disorder using valproate as a mood stabilizer.

Dr. Hadine Joffe, the lead author, is director of endocrine studies in the perinatal and reproductive psychiatry clinical research program at Massachusetts General Hospital in Boston.

She and her colleagues recommended warning women of PCOS risk before starting them on valproate.

Further, women on valproate should be evaluated for PCOS if they develop menstrual irregularities with hyperandrogenic symptoms. Along with PCOS treatment, the investigators suggested that “it may also be appropriate to consider alternative mood stabilizers if PCOS features develop on valproate.”

In an address at a psychiatric symposium sponsored by the University of Arizona, Dr. Gary Sachs, senior author and principal investigator of STEP-BD, emphasized the need for vigilance during the first year a patient is on valproate.

“Before you start women on valproate, you absolutely have to warn them this is a risk,” Dr. Sachs, founder and director of the bipolar clinic and research program at Massachusetts General Hospital, told psychiatrists at the Santa Fe, N.M., symposium, which was also sponsored by the University of Texas Southwestern Medical Center at Dallas and the University of New Mexico.

Sponsored by the National Institute of Mental Health, STEP-BD enrolled 4,361 patients in the largest clinical study to date on the treatment of bipolar disorder. Dr. Sachs said that Abbott Laboratories, which sells valproate under the brand name Depakote, was among the drug companies that supported the trial.

“They were very confident the risk wasn't there,” he said. “It turned out that was wrong. There really was a risk. The risks are there and published.”

To study the relationship in a nonepileptic population, the investigators sought out women aged 18–45 years in STEP-BD who were taking at least one mood stabilizer for at least 3 months.

Participants who had discontinued another mood stabilizer within the previous 3 months were not included in the substudy.

Of the 300 identified eligible women, 14 patients previously diagnosed with PCOS and three others with disorders involving oligomenorrhea were among those excluded from the sample. All told, 230 women were available for the analysis.

Of the valproate users, 12 developed oligomenorrhea, and 9 of them also had hirsutism, according to the report.

Among all patients with oligomenorrhea, valproate users had fewer menstrual cycles (median of 5 vs. 8.5 per year) than did nonusers.

Some had elevated total or free testosterone, moderate to severe acne, or male-pattern alopecia.

The valproate users who developed oligomenorrhea with hyperandrogenism had a higher median body mass index (kg/m

“Our study raises the possibility that increased body weight, insulin resistance, PCO morphology, younger age of first valproate use, and polypharmacy may predispose to the development of PCOS features on valproate,” the investigators concluded.

Women taking valproate for bipolar disorder are at significantly increased risk of developing features of polycystic ovary syndrome, according to a published study of 230 female patients in the Systematic Treatment Enhancement Program for Bipolar Disorder (STEP-BD) trial.

Investigators reported finding new-onset oligomenorrhea with hyperandrogenism in 9 (10.5%) of 86 women treated with valproate (Biol. Psychiatry 2006;59:1078–86).

Only 2 (1.4%) of 144 women on lithium or an anticonvulsant other than valproate developed these symptoms of polycystic ovary syndrome (PCOS).

In all cases, oligomenorrhea began within a year of the patient's starting valproate use. The investigators calculated the relative risk as 7.5 for women with bipolar disorder using valproate as a mood stabilizer.

Dr. Hadine Joffe, the lead author, is director of endocrine studies in the perinatal and reproductive psychiatry clinical research program at Massachusetts General Hospital in Boston.

She and her colleagues recommended warning women of PCOS risk before starting them on valproate.

Further, women on valproate should be evaluated for PCOS if they develop menstrual irregularities with hyperandrogenic symptoms. Along with PCOS treatment, the investigators suggested that “it may also be appropriate to consider alternative mood stabilizers if PCOS features develop on valproate.”

In an address at a psychiatric symposium sponsored by the University of Arizona, Dr. Gary Sachs, senior author and principal investigator of STEP-BD, emphasized the need for vigilance during the first year a patient is on valproate.

“Before you start women on valproate, you absolutely have to warn them this is a risk,” Dr. Sachs, founder and director of the bipolar clinic and research program at Massachusetts General Hospital, told psychiatrists at the Santa Fe, N.M., symposium, which was also sponsored by the University of Texas Southwestern Medical Center at Dallas and the University of New Mexico.

Sponsored by the National Institute of Mental Health, STEP-BD enrolled 4,361 patients in the largest clinical study to date on the treatment of bipolar disorder. Dr. Sachs said that Abbott Laboratories, which sells valproate under the brand name Depakote, was among the drug companies that supported the trial.

“They were very confident the risk wasn't there,” he said. “It turned out that was wrong. There really was a risk. The risks are there and published.”

To study the relationship in a nonepileptic population, the investigators sought out women aged 18–45 years in STEP-BD who were taking at least one mood stabilizer for at least 3 months.

Participants who had discontinued another mood stabilizer within the previous 3 months were not included in the substudy.

Of the 300 identified eligible women, 14 patients previously diagnosed with PCOS and three others with disorders involving oligomenorrhea were among those excluded from the sample. All told, 230 women were available for the analysis.

Of the valproate users, 12 developed oligomenorrhea, and 9 of them also had hirsutism, according to the report.

Among all patients with oligomenorrhea, valproate users had fewer menstrual cycles (median of 5 vs. 8.5 per year) than did nonusers.

Some had elevated total or free testosterone, moderate to severe acne, or male-pattern alopecia.

The valproate users who developed oligomenorrhea with hyperandrogenism had a higher median body mass index (kg/m

“Our study raises the possibility that increased body weight, insulin resistance, PCO morphology, younger age of first valproate use, and polypharmacy may predispose to the development of PCOS features on valproate,” the investigators concluded.