- 영문명
- 발행기관
- 대한소아신경학회
- 저자명
- Kyo Un Cho Donghwa Yang
- 간행물 정보
- 『Annals of Child Neurology(구 대한소아신경학회지)』vol.33 no.3, 114~120쪽, 전체 7쪽
- 주제분류
- 의약학 > 소아과학
- 파일형태
- 발행일자
- 2025.07.31
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국문 초록
Purpose: Headaches are common in pediatric patients and often require preventive treatment. Recent studies in adults suggest that low folate levels may contribute to headaches. However, research on folic acid supplementation for pediatric headaches remains limited. This study evaluated the effects of folic acid supplementation on pediatric migraine disorders and tension-type headaches.
Methods: We retrospectively reviewed medical records of pediatric patients with headaches who received folic acid supplementation between January 2021 and December 2024. Folate levels, headache frequency, and pain severity were analyzed. The primary outcome was the reduction in headache frequency and severity 2 months after supplementation. Responders were defined as patients whose headache frequency or pain severity decreased by more than 50% following treatment.
Results: Among 82 patients, 60 (73.2%) were classified as responders and 22 (26.8%) as non-responders. No significant difference in baseline folate levels was observed between the two groups (P=0.42). Over 2 months of folic acid supplementation, headache intensity significantly decreased from 6.0 (interquartile range [IQR], 5.0 to 7.0) to 1.5 (IQR, 0 to 2.9) in responders (P<0.001). Headache frequency also significantly decreased in responders from a median of 6.0 days/week (IQR, 3.5 to 7.0) to 0.5 days/week (IQR, 0 to 2.0) (P<0.001). Tension-type headaches were significantly more common in the non-responder group (59.1%, P=0.04).
Conclusion: This study provides evidence that folic acid supplementation is an effective and safe treatment for pediatric patients with low plasma folate levels.
영문 초록
목차
Introduction
Materials and Methods
Results
Discussion
References
해당간행물 수록 논문
- Annals of Child Neurology(구 대한소아신경학회지) vol.33 no.3 Contents
- Ending the Diagnostic Odyssey: Making Whole-Exome/Genome Sequencing the First-Line Test for Global Developmental Delay
- A Rare Case of Epileptic Encephalopathy Caused by X-Linked ALG13 Gene Mutation in a 6-Year-Old Girl
- A Case of Acute Flaccid Myelitis in a 7-Year-Old Boy
- Effect of Acetazolamide in a Child with CACNA1A Channelopathy, Refractory Seizures, and ADHD
- Effects of Folic Acid Supplementation on Headache in Children
- Development of Psychiatric Disorders after Mild Head Trauma according to Birth History
- Real-World Efficacy and Tolerability of Switching from Oxcarbazepine to Eslicarbazepine Therapy in Children Aged 6 Years or Older with Focal Epilepsy
- Cerebral Infarction Associated with Acute Subdural Hematoma in Infants: A Rare Entity from Northeastern India
참고문헌
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- Annals of Child Neurology(구 대한소아신경학회지) vol.33 no.3 Contents
- Ending the Diagnostic Odyssey: Making Whole-Exome/Genome Sequencing the First-Line Test for Global Developmental Delay
- A Rare Case of Epileptic Encephalopathy Caused by X-Linked ALG13 Gene Mutation in a 6-Year-Old Girl
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