Valproic Acid Is Effective in Migraine Prophylaxis at Low Serum Levels: A Prospective Open-Label Study

Objective.—We evaluated the efficacy of prophylactic valproic acid treatment (6 months) on the frequency of migraine attacks and the number of migraine headache days with respect to serum levels. Background.—Valproic acid, a GABAergic drug, has been shown to be effective for migraine prophylaxis. Re...

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Veröffentlicht in:Headache 2001-09, Vol.41 (8), p.774-778
Hauptverfasser: Kinze, Stephan, Clauss, Michael, Reuter, Uwe, Wolf, Tilo, Dreier, Jens Peter, Einhäupl, Karl Max, Arnold, Guy
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container_end_page 778
container_issue 8
container_start_page 774
container_title Headache
container_volume 41
creator Kinze, Stephan
Clauss, Michael
Reuter, Uwe
Wolf, Tilo
Dreier, Jens Peter
Einhäupl, Karl Max
Arnold, Guy
description Objective.—We evaluated the efficacy of prophylactic valproic acid treatment (6 months) on the frequency of migraine attacks and the number of migraine headache days with respect to serum levels. Background.—Valproic acid, a GABAergic drug, has been shown to be effective for migraine prophylaxis. Results from several dose‐ and serum level‐adjusted studies have recommended valproic acid doses within a range of 500 to 1500 mg per day for migraine prophylaxis. Design and Methods.—In this prospective open‐label study, 52 patients received valproic acid doses of 300 to 1200 mg per day; 45 patients were treated per protocol. Valproic acid serum levels increased linearly in relation to the valproic acid dose and were between 21 and 107 μg/mL at the end of the treatment period. Patients were divided into two groups: those with valproic acid serum levels less than 50 μg/mL (group 1) and those with serum levels greater than 50 μg/mL (group 2). Results.—The frequency of migraine attacks was significantly reduced in group 1 from 3.5 ± 0.9 to 2.0 ± 0.9 attacks per month. Migraine headache days also decreased (6.4 ± 3.5 to 4.6 ± 2.9 days per month). In the high serum level group, a reduction of migraine attacks from 3.5 ± 0.9 to 2.8 ± 1.0 attacks per month and only a slight decrease in headache days (6.4 ± 3.5 to 6.1 ± 2.4 days per month) was observed. The outcome of group 1 (low serum level) was significantly better than that of group 2 with respect to both parameters (P
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Background.—Valproic acid, a GABAergic drug, has been shown to be effective for migraine prophylaxis. Results from several dose‐ and serum level‐adjusted studies have recommended valproic acid doses within a range of 500 to 1500 mg per day for migraine prophylaxis. Design and Methods.—In this prospective open‐label study, 52 patients received valproic acid doses of 300 to 1200 mg per day; 45 patients were treated per protocol. Valproic acid serum levels increased linearly in relation to the valproic acid dose and were between 21 and 107 μg/mL at the end of the treatment period. Patients were divided into two groups: those with valproic acid serum levels less than 50 μg/mL (group 1) and those with serum levels greater than 50 μg/mL (group 2). Results.—The frequency of migraine attacks was significantly reduced in group 1 from 3.5 ± 0.9 to 2.0 ± 0.9 attacks per month. Migraine headache days also decreased (6.4 ± 3.5 to 4.6 ± 2.9 days per month). In the high serum level group, a reduction of migraine attacks from 3.5 ± 0.9 to 2.8 ± 1.0 attacks per month and only a slight decrease in headache days (6.4 ± 3.5 to 6.1 ± 2.4 days per month) was observed. The outcome of group 1 (low serum level) was significantly better than that of group 2 with respect to both parameters (P&lt;.05). Side effects were generally mild and temporary. Conclusions.—Due to the lack of additional benefit from higher valproic acid doses (more than 600 mg per day), we recommend daily valproic acid doses of 500 to 600 mg with a target serum level less than 50 μg/mL for the prophylactic treatment of migraine.</description><identifier>ISSN: 0017-8748</identifier><identifier>EISSN: 1526-4610</identifier><identifier>DOI: 10.1046/j.1526-4610.2001.01142.x</identifier><identifier>PMID: 11576201</identifier><identifier>CODEN: HEADAE</identifier><language>eng</language><publisher>Boston, MA, USA: Blackwell Science Inc</publisher><subject>Anticonvulsants - administration &amp; dosage ; Anticonvulsants - blood ; Anticonvulsants - therapeutic use ; Biological and medical sciences ; Cardiovascular system ; Dose-Response Relationship, Drug ; Female ; headache ; Humans ; Male ; Medical sciences ; Middle Aged ; Migraine Disorders - prevention &amp; control ; migraine prophylaxis ; Pharmacology. Drug treatments ; Prospective Studies ; treatment ; valproate ; Valproic Acid - administration &amp; dosage ; Valproic Acid - blood ; Valproic Acid - therapeutic use ; Vasodilator agents. Cerebral vasodilators</subject><ispartof>Headache, 2001-09, Vol.41 (8), p.774-778</ispartof><rights>2001 INIST-CNRS</rights><rights>Copyright Blackwell Publishing Ltd. 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Background.—Valproic acid, a GABAergic drug, has been shown to be effective for migraine prophylaxis. Results from several dose‐ and serum level‐adjusted studies have recommended valproic acid doses within a range of 500 to 1500 mg per day for migraine prophylaxis. Design and Methods.—In this prospective open‐label study, 52 patients received valproic acid doses of 300 to 1200 mg per day; 45 patients were treated per protocol. Valproic acid serum levels increased linearly in relation to the valproic acid dose and were between 21 and 107 μg/mL at the end of the treatment period. Patients were divided into two groups: those with valproic acid serum levels less than 50 μg/mL (group 1) and those with serum levels greater than 50 μg/mL (group 2). Results.—The frequency of migraine attacks was significantly reduced in group 1 from 3.5 ± 0.9 to 2.0 ± 0.9 attacks per month. Migraine headache days also decreased (6.4 ± 3.5 to 4.6 ± 2.9 days per month). In the high serum level group, a reduction of migraine attacks from 3.5 ± 0.9 to 2.8 ± 1.0 attacks per month and only a slight decrease in headache days (6.4 ± 3.5 to 6.1 ± 2.4 days per month) was observed. The outcome of group 1 (low serum level) was significantly better than that of group 2 with respect to both parameters (P&lt;.05). Side effects were generally mild and temporary. Conclusions.—Due to the lack of additional benefit from higher valproic acid doses (more than 600 mg per day), we recommend daily valproic acid doses of 500 to 600 mg with a target serum level less than 50 μg/mL for the prophylactic treatment of migraine.</description><subject>Anticonvulsants - administration &amp; dosage</subject><subject>Anticonvulsants - blood</subject><subject>Anticonvulsants - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Cardiovascular system</subject><subject>Dose-Response Relationship, Drug</subject><subject>Female</subject><subject>headache</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Migraine Disorders - prevention &amp; control</subject><subject>migraine prophylaxis</subject><subject>Pharmacology. Drug treatments</subject><subject>Prospective Studies</subject><subject>treatment</subject><subject>valproate</subject><subject>Valproic Acid - administration &amp; dosage</subject><subject>Valproic Acid - blood</subject><subject>Valproic Acid - therapeutic use</subject><subject>Vasodilator agents. 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Background.—Valproic acid, a GABAergic drug, has been shown to be effective for migraine prophylaxis. Results from several dose‐ and serum level‐adjusted studies have recommended valproic acid doses within a range of 500 to 1500 mg per day for migraine prophylaxis. Design and Methods.—In this prospective open‐label study, 52 patients received valproic acid doses of 300 to 1200 mg per day; 45 patients were treated per protocol. Valproic acid serum levels increased linearly in relation to the valproic acid dose and were between 21 and 107 μg/mL at the end of the treatment period. Patients were divided into two groups: those with valproic acid serum levels less than 50 μg/mL (group 1) and those with serum levels greater than 50 μg/mL (group 2). Results.—The frequency of migraine attacks was significantly reduced in group 1 from 3.5 ± 0.9 to 2.0 ± 0.9 attacks per month. Migraine headache days also decreased (6.4 ± 3.5 to 4.6 ± 2.9 days per month). In the high serum level group, a reduction of migraine attacks from 3.5 ± 0.9 to 2.8 ± 1.0 attacks per month and only a slight decrease in headache days (6.4 ± 3.5 to 6.1 ± 2.4 days per month) was observed. The outcome of group 1 (low serum level) was significantly better than that of group 2 with respect to both parameters (P&lt;.05). Side effects were generally mild and temporary. Conclusions.—Due to the lack of additional benefit from higher valproic acid doses (more than 600 mg per day), we recommend daily valproic acid doses of 500 to 600 mg with a target serum level less than 50 μg/mL for the prophylactic treatment of migraine.</abstract><cop>Boston, MA, USA</cop><pub>Blackwell Science Inc</pub><pmid>11576201</pmid><doi>10.1046/j.1526-4610.2001.01142.x</doi><tpages>5</tpages></addata></record>
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subjects Anticonvulsants - administration & dosage
Anticonvulsants - blood
Anticonvulsants - therapeutic use
Biological and medical sciences
Cardiovascular system
Dose-Response Relationship, Drug
Female
headache
Humans
Male
Medical sciences
Middle Aged
Migraine Disorders - prevention & control
migraine prophylaxis
Pharmacology. Drug treatments
Prospective Studies
treatment
valproate
Valproic Acid - administration & dosage
Valproic Acid - blood
Valproic Acid - therapeutic use
Vasodilator agents. Cerebral vasodilators
title Valproic Acid Is Effective in Migraine Prophylaxis at Low Serum Levels: A Prospective Open-Label Study
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