Low Serum Pyridoxine Levels Worsen Seizure Control in Adult Epilepsy Patients.

breakthrough seizures poorly controlled epilepsy pyridoxine vitamin b6 vitamin deficiency

Journal

Cureus
ISSN: 2168-8184
Titre abrégé: Cureus
Pays: United States
ID NLM: 101596737

Informations de publication

Date de publication:
Jun 2022
Historique:
accepted: 05 06 2022
entrez: 11 7 2022
pubmed: 12 7 2022
medline: 12 7 2022
Statut: epublish

Résumé

Vitamin B6 (pyridoxine) is an important cofactor in the process by which glutamic acid decarboxylase (GAD) converts the excitatory, pro-epileptogenic neurotransmitter, glutamate, into the inhibitory, anti-epileptogenic neurotransmitter, gamma-aminobutyric acid (GABA). This concept has been established in infants with pyridoxine-dependent epilepsy as well as adult patients with other epilepsy subtypes who presented with medication-resistant status epilepticus, with both patient groups experiencing cessation of seizure activity following pyridoxine administration. Given our knowledge of the role of vitamin B6 in the conversion of glutamate to GABA, its effect on seizure control in infants with specific epilepsy subtypes, reports of adult-onset seizures associated with vitamin B6 deficiency, and vitamin B6's role in terminating status epilepticus in adult patients with other types of epilepsy, we suspect that low vitamin B6 levels in adult epilepsy patients may correlate with poor seizure control across all epilepsy subtypes. This study seeks to determine whether there is a relationship between pyridoxine levels and the level of seizure control in adults with epilepsy, regardless of their seizure type. After obtaining institutional review board approval, we prospectively enrolled 32 patients (age range: 25-57 years) with epilepsy who presented to our clinic. Patients who did not meet the study criteria or who were diagnosed with psychogenic non-epileptic seizures (PNES) were excluded from the study (n = 2). Patients were classified as well-controlled (WC) or poorly controlled (PC) based on the absence or presence of a seizure within the last three months, respectively. After classification as WC or PC, pyridoxine serum levels and anti-seizure medication (ASM) levels were drawn in that clinic visit, following patient consent. All patients were contacted regarding pyridoxine and serum ASM levels, and patients that were found to be deficient in pyridoxine were treated with appropriate supplementation. At the end of the recruitment period, we performed analyses to determine if there was a statistically significant relationship between PC status and serum pyridoxine levels. Of 32 patients, two patients were diagnosed with psychogenic non-epileptic events and were subsequently excluded. Of 30 patients, 10 had PC epilepsy. Median (interquartile range) serum B6 levels were 35.8 (26.8-54.2) in patients with WC epilepsy and 17.5 (10.1-41.3) in patients with PC epilepsy (P = 0.11). In the PC group, 6/10 (60%) of the patients demonstrated low serum pyridoxine compared to 3/20 (15%) in the WC group (P = 0.03). There was a statistically significant relationship between serum pyridoxine levels and seizure control. If appropriate, pyridoxine supplementation should be considered, especially in critically ill adult patients with refractory or PC seizures despite good adherence to ASMs.

Sections du résumé

BACKGROUND BACKGROUND
Vitamin B6 (pyridoxine) is an important cofactor in the process by which glutamic acid decarboxylase (GAD) converts the excitatory, pro-epileptogenic neurotransmitter, glutamate, into the inhibitory, anti-epileptogenic neurotransmitter, gamma-aminobutyric acid (GABA). This concept has been established in infants with pyridoxine-dependent epilepsy as well as adult patients with other epilepsy subtypes who presented with medication-resistant status epilepticus, with both patient groups experiencing cessation of seizure activity following pyridoxine administration. Given our knowledge of the role of vitamin B6 in the conversion of glutamate to GABA, its effect on seizure control in infants with specific epilepsy subtypes, reports of adult-onset seizures associated with vitamin B6 deficiency, and vitamin B6's role in terminating status epilepticus in adult patients with other types of epilepsy, we suspect that low vitamin B6 levels in adult epilepsy patients may correlate with poor seizure control across all epilepsy subtypes. This study seeks to determine whether there is a relationship between pyridoxine levels and the level of seizure control in adults with epilepsy, regardless of their seizure type.
METHODS METHODS
After obtaining institutional review board approval, we prospectively enrolled 32 patients (age range: 25-57 years) with epilepsy who presented to our clinic. Patients who did not meet the study criteria or who were diagnosed with psychogenic non-epileptic seizures (PNES) were excluded from the study (n = 2). Patients were classified as well-controlled (WC) or poorly controlled (PC) based on the absence or presence of a seizure within the last three months, respectively. After classification as WC or PC, pyridoxine serum levels and anti-seizure medication (ASM) levels were drawn in that clinic visit, following patient consent. All patients were contacted regarding pyridoxine and serum ASM levels, and patients that were found to be deficient in pyridoxine were treated with appropriate supplementation. At the end of the recruitment period, we performed analyses to determine if there was a statistically significant relationship between PC status and serum pyridoxine levels.
RESULTS RESULTS
Of 32 patients, two patients were diagnosed with psychogenic non-epileptic events and were subsequently excluded. Of 30 patients, 10 had PC epilepsy. Median (interquartile range) serum B6 levels were 35.8 (26.8-54.2) in patients with WC epilepsy and 17.5 (10.1-41.3) in patients with PC epilepsy (P = 0.11). In the PC group, 6/10 (60%) of the patients demonstrated low serum pyridoxine compared to 3/20 (15%) in the WC group (P = 0.03).
CONCLUSION CONCLUSIONS
There was a statistically significant relationship between serum pyridoxine levels and seizure control. If appropriate, pyridoxine supplementation should be considered, especially in critically ill adult patients with refractory or PC seizures despite good adherence to ASMs.

Identifiants

pubmed: 35812624
doi: 10.7759/cureus.25669
pmc: PMC9256010
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e25669

Informations de copyright

Copyright © 2022, Rane et al.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

Références

Epilepsy Res Treat. 2013;2013:510529
pubmed: 23984056
Epilepsia. 2001;42 Suppl 3:8-12
pubmed: 11520315
Pharmacotherapy. 2006 Oct;26(10):1529-32
pubmed: 16999664
Ann N Y Acad Sci. 1990;585:250-60
pubmed: 2162644
Epilepsy Behav. 2015 Nov;52(Pt A):154-8
pubmed: 26418265
Pediatrics. 1954 Feb;13(2):140-5
pubmed: 13133562
Intractable Rare Dis Res. 2014 May;3(2):52-6
pubmed: 25343127
J Nutr. 2000 Apr;130(4S Suppl):1043S-5S
pubmed: 10736378
J Epilepsy Res. 2015 Jun 30;5(1):23-4
pubmed: 26157671
J Perinatol. 2009 Mar;29(3):252-3
pubmed: 19240731
JPEN J Parenter Enteral Nutr. 2011 Mar;35(2):272-5
pubmed: 21378258

Auteurs

Schweta Rane (S)

Neurology, University of Texas Medical Branch, Galveston, USA.

Sama Elrahi (S)

Neurology, University of Texas Medical Branch, Galveston, USA.

Joseph Villarreal (J)

Neurology, University of Texas Medical Branch, Galveston, USA.

Haneef Zulfi (H)

Neurology, Baylor College of Medicine, Houston, USA.

Xiang Fang (X)

Neurology, University of Texas Medical Branch, Galveston, USA.

Daniel Graf (D)

Neurology, Geisinger Commonwealth School of Medicine, Scranton, USA.

Rafael Rodriguez (R)

Neurology, St. Joseph's Hospital, Tampa, USA.

Amanda Garza (A)

Neurology, University of Texas Medical Branch, Galveston, USA.

Neeharika Thottempudi (N)

Neurology, University of Texas Medical Branch, Galveston, USA.

Prashant Rai (P)

Neurology, University of Texas Medical Branch, Galveston, USA.

Todd Masel (T)

Neurology, University of Texas Medical Branch, Galveston, USA.

Classifications MeSH