Endocrine and metabolic abnormalities involved in obesity associated with typical antipsychotic drug administration

In this study, the authors assessed the endocrine system and glucose tolera nce in obese and non-obese women chronically treated with typical antipsych otic drugs (AP). In particular, we tested the hypotheses that these subject s display hypogonadism and increased insulin resistance compared to healthy weight-matched controls, as these abnormalities create a tendency towards excessive body weight gain. Twenty-six AP-treated women were matched with 2 6 healthy women by age, body mass index and day of the menstrual cycle. The following serum variables were evaluated in each subject: glucose toleranc e after an oral glucose overload, insulin, leptin, beta -endorphin, reprodu ctive hormones, adrenal steroids and lipids. Compared to controls, AP-treat ed women displayed significantly higher levels of basal glucose, insulin af ter 60 min of the glucose overload, prolactin, thyroid stimulating hormone and beta -endorphin, with lower levels of C-Peptide, progesterone, 17-OH pr ogesterone, androstenedione and high-density lipoprotein cholesterol. The l evels of estradiol, estrone and leptin did not differ between the groups. T hus, women treated with typical AP appeared to display more insulin resista nce than healthy controls, predisposing them to excessive weight gain. Insu lin sensitivity might be further impaired when the subject switches to atyp ical AP administration. Metformin and related agents may reduce body weight in these subjects. The high levels of the opiate beta -endorphin suggest t hat opiate antagonists such as naloxone and naltrexone might be useful as w ell. Even though the luteal phase of the menstrual cycle appears to be seve rely disturbed, the normal serum levels of estradiol and estrone do not sup port the proposal derived from animal experimental studies about the use of estrogens or tamoxifen to counteract AP-induced obesity.