Topiramate chemical structure
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Topiramate

Topiramate (brand name: Topamax®) is an anticonvulsant drug produced by Ortho-McNeil, a division of Johnson & Johnson. It is used to treat epilepsy in both children and adults. In children it is also indicated for treatment of Lennox-Gastaut syndrome (a disorder that causes seizures and developmental delays). It is also FDA approved for, and now most frequently prescribed for, the prevention of migraines. It has been used by psychiatrists to treat bipolar disorder, although it is not FDA approved for this purpose and such use is somewhat controversial. more...

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This drug has been investigated for use in treatment of obesity, especially to aid in the reduction of binge eating, and also as a possible treatment for alcoholism. However, these uses are not actively promoted by the manufacturer, and like its use for bipolar disorder, are "off-label" uses. The drug is also used in clinical trials to treat Post Traumatic Stress Disorder. A pilot study suggests that Topiramate is possibly effective against infantile spasm.

Pharmacodynamics

Chemically, Topiramate is a sulfamate-substituted monosaccharide, related to fructose, a rather unusual chemical structure for an anticonvulsant. Topiramate is quickly absorbed after oral use. Most of the drug (70%) is excreted in the urine as unchanged drug. The remainder is extensively metabolized by hydroxylation, hydrolysis, and glucuronidation. Six metabolites have been identified in humans, none of which constitutes more than 5% of an administered dose. Topiramate enhances GABA-activated chloride channels. In addition, Topiramate inhibits excitatory neurotransmission, through actions on kainate and AMPA receptors. There is evidence that Topiramate has a specific effect on GluR5 kainate receptors. It is also an inhibitor of carbonic anhydrase, particular subtypes II and IV, but this action is weak and unlikely to be related to its anticonvulsant actions, but may account for the bad taste and the development of renal stones seen during treatment. Its possible effect as a mood stabilizer seems to occur before anticonvulsant qualities at lower dosages. Topiramate inhibits maximal electroshock and pentylenetetrazol-induced seizures as well as partial and secundarily generalized tonic-clonic seizures in the kindling model, findings predective of a broad spectrum of antiseizure activities clinically.

Side effects

The most common side effects include a change in taste (carbonated beverages, especially diet sodas and beer, taste particularly bad) and feelings of pins and needles in the head and extremities. Less common side effects include cognitive deficiency (particularly word-finding difficulty); grogginess; lethargy; renal stones, impairment of fine motor skills; vision abnormality and transient or permanent vision loss (see below for FDA warning); weight loss; breast pain; abdominal pain; menstrual disorder; taste changes; pharyngitis; sinusitis; diplopia; rash; leukopenia; fatigue; dizziness; insomnia; anxiety; depression; paresthesia; diarrhea; nausea; dyspepsia; constipation; dry-mouth; dysmenorrhea.

Rarely, the inhibition of carbonic anhydrase may be strong enough to cause metabolic acidosis of clinical importance.

The side-effects most frequently leading to discontinuation of therapy with topiramate were :

Read more at Wikipedia.org


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Topiramate treatment in alcohol-dependent patients
From American Family Physician, 8/1/05 by Karl E. Miller

Topiramate (Topamax) has been shown to be effective in reducing alcohol cravings, decreasing heavy drinking, and improving abstinence rates in patients who are alcohol dependent. Despite being an established pharmacotherapy agent for alcohol abstinence, questions about this medication persist. Does topiramate improve drinking outcomes because it improves quality of life, or does it reduce the harmful consequences of alcohol abuse? This question is difficult to answer because alcohol dependence syndrome has a negative impact on social, occupational, and recreational activities. In addition, past studies on topiramate were coupled with psychotherapy. Johnson and colleagues evaluated topiramate alone and its effect on psychosocial functioning in alcohol-dependent patients.

The study was a double-blind, randomized, controlled clinical trial comparing topiramate with placebo in alcohol-dependent patients. Participants were eligible for the study if they were adults, met the Diagnostic and Statistical Manual of Mental Disorders, 4th ed., criteria for alcohol dependence, and had a high score on an alcohol-use disorder test. In addition, participants had to have consumed a specified number of drinks during the previous 90 days (i.e., at least 21 for women, 35 for men). The intervention group received topiramate starting at a dosage of 25 mg per day and increasing to as much as 300 mg per day. The study duration was 12 weeks. Participants received a brief compliance-enhancement procedure at baseline and at weekly intervals. The main outcomes measured included clinical ratings of psychosocial functioning, alcohol-dependence severity, quality of life, and harmful drinking consequences.

A total of 150 patients completed the study. Compared with placebo, topiramate significantly improved overall well-being and life satisfaction. In addition, topiramate significantly improved reported abstinence rates and reduced harmful drinking consequences. The percentage of heavy-drinking days shifted significantly from higher to lower drinking quartiles in the topiramate group. This was associated with improvements in all psychosocial measurements.

The authors conclude that topiramate as an adjuvant to a medication-compliance program was superior to placebo in improving drinking outcomes. In addition, topiramate had a positive impact on the overall well-being and quality of life in patients with alcohol dependence. This intervention also reduced dependence severity and its harmful consequences in these patients.

Johnson BA, et al. Oral topiramate reduces the consequences of drinking and improves quality of life of alcohol-dependent individuals. Arch Gen Psychiatry September 2004;61:905-12.

COPYRIGHT 2005 American Academy of Family Physicians
COPYRIGHT 2005 Gale Group

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