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1.
Epilepsia ; 53(12): 2172-7, 2012 Dec.
Article in English | MEDLINE | ID: mdl-22958083

ABSTRACT

PURPOSE: The present study aimed to assess bone mineral density (BMD) in a population of children and adolescents with cerebral palsy and mental retardation with or without epilepsy. METHODS: One hundred thirteen patients (63 male and 50 female) were recruited for evaluation. Patients were divided in three groups: 40 patients (group 1) were affected by cerebral palsy and mental retardation; 47 (group 2) by cerebral palsy, mental retardation, and epilepsy; and 26 (group 3) by epilepsy. The control group consisted of 63 healthy children and adolescents. Patients underwent a dual-energy x-ray absorptiometry (DEXA) scan of the lumbar spine (L1-L4), and z-score was calculated for each patient; t-score was considered for patients 18 years of age and older. KEY FINDINGS: Abnormal BMD by DEXA was found in 17 patients (42.5%) in group 1, in 33 (70.2%) in group 2, and in 3 (11.5%) in group 3. In groups 1 and 2, tetraparesis and severe/profound mental retardation were related to a significantly abnormal BMD (p = 0.003). The multivariate analysis of independent factors on BMD (z-score) revealed a significant correlation between BMD (z-score) and age (p = 0.04), body mass index (BMI; p = 0.002), severe/profound mental retardation (p = 0.03), and epilepsy (p = 0.05). SIGNIFICANCE: A significantly lower BMD z-score value was found in patients with cerebral palsy, mental retardation, and epilepsy compared with those without epilepsy. The epileptic disorder appears to be an aggravating factor on bone health when comorbid with cerebral palsy and mental retardation.


Subject(s)
Bone Density , Cerebral Palsy/physiopathology , Epilepsy/complications , Epilepsy/epidemiology , Intellectual Disability/complications , Intellectual Disability/epidemiology , Absorptiometry, Photon , Adolescent , Cerebral Palsy/diagnostic imaging , Cerebral Palsy/epidemiology , Child , Child, Preschool , Community Health Planning , Epilepsy/diagnostic imaging , Female , Humans , Male , Multivariate Analysis , Severity of Illness Index
2.
Epilepsia ; 50(9): 2140-6, 2009 Sep.
Article in English | MEDLINE | ID: mdl-19486359

ABSTRACT

PURPOSE: The aim of this study was to assess bone mineral density (BMD) in a large population of children, adolescents, and young adults with epilepsy alone or in association with cerebral palsy and/or mental retardation. METHODS: Ninety-six patients were enrolled in the study. The group comprised 50 males and 46 females, aged between 3 and 25 years (mean age 11 years). The control group consisted of 63 healthy children and adolescents (23 males, 40 females), aged between 3 and 25 years (mean age 12.1 years). Patients underwent a dual-energy x-ray absorptiometry (DEXA) scan of the lumbar spine (L1-L4) and the z scores were calculated for each patient; the t score was considered for patients 18 years of age or older. RESULTS: Abnormal BMD was found in 56 patients (58.3%), with values documenting osteopenia in 42 (75%) and osteoporosis in 14 (25%). A significant difference emerged between epileptic patients and the control group in BMD, z score, and body mass index (BMI) (p = <0.001). Lack of autonomous gait, severe mental retardation, long duration of antiepileptic treatment, topiramate adjunctive therapy, and less physical activity significantly correlated with abnormal BMD. DISCUSSION: This study detected abnormal BMD in more than half of a large pediatric population with epilepsy with or without cerebral palsy and/or mental retardation. The clinical significance of these findings has yet to be clarified.


Subject(s)
Bone Density , Epilepsy/diagnostic imaging , Osteoporosis/diagnostic imaging , Absorptiometry, Photon/statistics & numerical data , Adolescent , Adult , Age Factors , Anticonvulsants/adverse effects , Anticonvulsants/therapeutic use , Body Mass Index , Cerebral Palsy/epidemiology , Child , Child, Preschool , Comorbidity , Epilepsy/drug therapy , Epilepsy/epidemiology , Female , Humans , Intellectual Disability/epidemiology , Lumbar Vertebrae/diagnostic imaging , Male , Motor Activity , Osteoporosis/drug therapy , Osteoporosis/epidemiology , Risk Factors , Young Adult
3.
Pediatr Neurol ; 37(6): 411-6, 2007 Dec.
Article in English | MEDLINE | ID: mdl-18021922

ABSTRACT

Our aim was to evaluate bone mineral densitometry in patients with Angelman syndrome with or without antiepileptic therapy. Eighteen patients (9 females, 9 males), aged 4.0-24.3 years (mean age, 10.1 years), and two control groups consisting of 18 epileptic and 24 healthy patients, underwent dual-energy X-ray absorptiometry at the lumbar spine (L(1)-L(4)), and z score was evaluated for each patient; the t score was considered for patients aged > or = 18 years. Abnormal bone mineral density was present in 8/18 (44.5%) of patients with Angelman syndrome, in 7/18 (38.9%) of the epileptic group, and in none of the healthy controls. Furthermore, a significant difference regarding mean age of patients (6 versus 15 years, P = 0.008, by Fisher exact test), and mean length of drug treatment (3.5 versus 11.1 years, P = 0.005 by Fisher exact test), appeared in the group with Angelman syndrome. Most of these patients (94.4%) were receiving antiepileptic drugs, mainly valproic acid, for many years. In conclusion, our study revealed osteopenia in almost half the children and young patients with Angelman syndrome. Dual-energy X-ray absorptiometry should be performed in all patients with Angelman syndrome, particularly if they are treated with antiepileptic drugs.


Subject(s)
Angelman Syndrome/physiopathology , Bone Density/physiology , Absorptiometry, Photon/methods , Adolescent , Adult , Child , Child, Preschool , Epilepsy/physiopathology , Female , Humans , Male
4.
Epileptic Disord ; 9(2): 145-8, 2007 Jun.
Article in English | MEDLINE | ID: mdl-17525023

ABSTRACT

A child had the characteristic clinical and EEG pattern of migrating partial seizures in infancy with left temporal lobe atrophy, hippocampal sclerosis and cortical-subcortical blurring. Seizures were drug-resistant, with recurring episodes of status epilepticus. The child developed microcephaly with arrest of psychomotor development. Focal brain lesions, in the context of migrating partial seizures, have not been previously reported.[Published with video sequences].


Subject(s)
Brain Diseases/diagnosis , Epilepsies, Partial/diagnosis , Hippocampus/pathology , Microcephaly/epidemiology , Temporal Lobe/pathology , Atrophy/pathology , Brain Diseases/epidemiology , Child, Preschool , Comorbidity , Electroencephalography/statistics & numerical data , Epilepsies, Partial/epidemiology , Epilepsy, Temporal Lobe/epidemiology , Epilepsy, Temporal Lobe/pathology , Female , Functional Laterality , Humans , Magnetic Resonance Imaging , Psychomotor Disorders/epidemiology , Psychomotor Disorders/pathology , Sclerosis/pathology , Status Epilepticus/diagnosis , Status Epilepticus/epidemiology
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