Incidence and classification of new-onset epilepsy and epilepsy syndromes in children in Olmsted County, Minnesota from 1980 to 2004

A population-based study

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Abstract

Purpose: To determine the incidence and classification of new-onset epilepsy, as well as the distribution of epilepsy syndromes in a population-based group of children, using the newly proposed Report of the ILAE Commission on Classification and Terminology 2005-2009. Methods: We identified all children residing in Olmsted County, MN, 1 month through 17. years with newly diagnosed epilepsy from 1980 to 2004. For each patient, epilepsy was classified into mode of onset, etiology, and syndrome or constellation (if present). Incidence rates were calculated overall and also separately for categories of mode of onset and etiology. Results: The adjusted incidence rate of new-onset epilepsy in children was 44.5 cases per 100,000 persons per year. Incidence rates were highest in the first year of life and diminished with age. Mode of onset was focal in 68%, generalized/bilateral in 23%, spasms in 3% and unknown in 5%. Approximately half of children had an unknown etiology for their epilepsy, and of the remainder, 78 (22%) were genetic and 101 (28%) were structural/metabolic. A specific epilepsy syndrome could be defined at initial diagnosis in 99/359 (28%) children, but only 9/359 (3%) had a defined constellation. Conclusion: Nearly half of childhood epilepsy is of " unknown" etiology. While a small proportion of this group met criteria for a known epilepsy syndrome, 41% of all childhood epilepsy is of " unknown" cause with no clear syndrome identified. Further work is needed to define more specific etiologies for this group.

Original languageEnglish (US)
Pages (from-to)110-118
Number of pages9
JournalEpilepsy Research
Volume95
Issue number1-2
DOIs
StatePublished - Jun 2011

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Epilepsy
Incidence
Population
Spasm
Population Groups
Terminology

Keywords

  • Epilepsy syndrome
  • Incidence
  • Pediatric epilepsy

ASJC Scopus subject areas

  • Clinical Neurology
  • Neurology

Cite this

@article{7559e346d6604a01a361f1ae9279e5e9,
title = "Incidence and classification of new-onset epilepsy and epilepsy syndromes in children in Olmsted County, Minnesota from 1980 to 2004: A population-based study",
abstract = "Purpose: To determine the incidence and classification of new-onset epilepsy, as well as the distribution of epilepsy syndromes in a population-based group of children, using the newly proposed Report of the ILAE Commission on Classification and Terminology 2005-2009. Methods: We identified all children residing in Olmsted County, MN, 1 month through 17. years with newly diagnosed epilepsy from 1980 to 2004. For each patient, epilepsy was classified into mode of onset, etiology, and syndrome or constellation (if present). Incidence rates were calculated overall and also separately for categories of mode of onset and etiology. Results: The adjusted incidence rate of new-onset epilepsy in children was 44.5 cases per 100,000 persons per year. Incidence rates were highest in the first year of life and diminished with age. Mode of onset was focal in 68{\%}, generalized/bilateral in 23{\%}, spasms in 3{\%} and unknown in 5{\%}. Approximately half of children had an unknown etiology for their epilepsy, and of the remainder, 78 (22{\%}) were genetic and 101 (28{\%}) were structural/metabolic. A specific epilepsy syndrome could be defined at initial diagnosis in 99/359 (28{\%}) children, but only 9/359 (3{\%}) had a defined constellation. Conclusion: Nearly half of childhood epilepsy is of {"} unknown{"} etiology. While a small proportion of this group met criteria for a known epilepsy syndrome, 41{\%} of all childhood epilepsy is of {"} unknown{"} cause with no clear syndrome identified. Further work is needed to define more specific etiologies for this group.",
keywords = "Epilepsy syndrome, Incidence, Pediatric epilepsy",
author = "Wirrell, {Elaine C} and Grossardt, {Brandon R.} and Lily Wong-Kisiel and Nickels, {Katherine C}",
year = "2011",
month = "6",
doi = "10.1016/j.eplepsyres.2011.03.009",
language = "English (US)",
volume = "95",
pages = "110--118",
journal = "Epilepsy Research",
issn = "0920-1211",
publisher = "Elsevier",
number = "1-2",

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T1 - Incidence and classification of new-onset epilepsy and epilepsy syndromes in children in Olmsted County, Minnesota from 1980 to 2004

T2 - A population-based study

AU - Wirrell, Elaine C

AU - Grossardt, Brandon R.

AU - Wong-Kisiel, Lily

AU - Nickels, Katherine C

PY - 2011/6

Y1 - 2011/6

N2 - Purpose: To determine the incidence and classification of new-onset epilepsy, as well as the distribution of epilepsy syndromes in a population-based group of children, using the newly proposed Report of the ILAE Commission on Classification and Terminology 2005-2009. Methods: We identified all children residing in Olmsted County, MN, 1 month through 17. years with newly diagnosed epilepsy from 1980 to 2004. For each patient, epilepsy was classified into mode of onset, etiology, and syndrome or constellation (if present). Incidence rates were calculated overall and also separately for categories of mode of onset and etiology. Results: The adjusted incidence rate of new-onset epilepsy in children was 44.5 cases per 100,000 persons per year. Incidence rates were highest in the first year of life and diminished with age. Mode of onset was focal in 68%, generalized/bilateral in 23%, spasms in 3% and unknown in 5%. Approximately half of children had an unknown etiology for their epilepsy, and of the remainder, 78 (22%) were genetic and 101 (28%) were structural/metabolic. A specific epilepsy syndrome could be defined at initial diagnosis in 99/359 (28%) children, but only 9/359 (3%) had a defined constellation. Conclusion: Nearly half of childhood epilepsy is of " unknown" etiology. While a small proportion of this group met criteria for a known epilepsy syndrome, 41% of all childhood epilepsy is of " unknown" cause with no clear syndrome identified. Further work is needed to define more specific etiologies for this group.

AB - Purpose: To determine the incidence and classification of new-onset epilepsy, as well as the distribution of epilepsy syndromes in a population-based group of children, using the newly proposed Report of the ILAE Commission on Classification and Terminology 2005-2009. Methods: We identified all children residing in Olmsted County, MN, 1 month through 17. years with newly diagnosed epilepsy from 1980 to 2004. For each patient, epilepsy was classified into mode of onset, etiology, and syndrome or constellation (if present). Incidence rates were calculated overall and also separately for categories of mode of onset and etiology. Results: The adjusted incidence rate of new-onset epilepsy in children was 44.5 cases per 100,000 persons per year. Incidence rates were highest in the first year of life and diminished with age. Mode of onset was focal in 68%, generalized/bilateral in 23%, spasms in 3% and unknown in 5%. Approximately half of children had an unknown etiology for their epilepsy, and of the remainder, 78 (22%) were genetic and 101 (28%) were structural/metabolic. A specific epilepsy syndrome could be defined at initial diagnosis in 99/359 (28%) children, but only 9/359 (3%) had a defined constellation. Conclusion: Nearly half of childhood epilepsy is of " unknown" etiology. While a small proportion of this group met criteria for a known epilepsy syndrome, 41% of all childhood epilepsy is of " unknown" cause with no clear syndrome identified. Further work is needed to define more specific etiologies for this group.

KW - Epilepsy syndrome

KW - Incidence

KW - Pediatric epilepsy

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