TY - JOUR
T1 - Dysautonomia and functional impairment in rare developmental and epileptic encephalopathies
T2 - the other nervous system
AU - Berg, Anne T.
AU - Coffman, Keith
AU - Gaebler-Spira, Deborah
N1 - Funding Information:
We are very grateful to the members of the Dravet Syndrome Foundation, Lennox–Gastaut Syndrome Foundation, KCNQ2 Cure Alliance, Jack Pribaz Foundation, KCNB1 parent group, CHD2 parent group, PACS1 Smiles, the ESES/CSWS/LKS parent group, and many others for their collaboration in designing, implementing, and participating in this study. This study would not have been possible without the expertise and collaboration of Gerry Nesbitt of CLIRINX, Dublin, Ireland. This work was supported by the Stanley Manne Children’s Research Institute and Ann & Robert H Lurie Children’s Hospital of Chicago under the Precision Medicine Strategic Research Initiative and by a grant from the Pediatric Epilepsy Research Foundation, Dallas, TX, USA. The authors have stated that they had no interests that might be perceived as posing conflict or bias.
Funding Information:
We are very grateful to the members of the Dravet Syndrome Foundation, Lennox?Gastaut Syndrome Foundation, KCNQ2 Cure Alliance, Jack Pribaz Foundation, KCNB1 parent group, CHD2 parent group, PACS1 Smiles, the ESES/CSWS/LKS parent group, and many others for their collaboration in designing, implementing, and participating in this study. This study would not have been possible without the expertise and collaboration of Gerry Nesbitt of CLIRINX, Dublin, Ireland. This work was supported by the Stanley Manne Children?s Research Institute and Ann & Robert H Lurie Children?s Hospital of Chicago under the Precision Medicine Strategic Research Initiative and by a grant from the Pediatric Epilepsy Research Foundation, Dallas, TX, USA. The authors have stated that they had no interests that might be perceived as posing conflict or bias.
Publisher Copyright:
© 2021 Mac Keith Press.
PY - 2021/12
Y1 - 2021/12
N2 - Aim: To determine whether functional impairments and autonomic symptoms are correlated in young people with developmental and epileptic encephalopathies (DEEs). Method: Cross-sectional, online surveys (2018–2020) of parents recruited from family groups obtained information on several aspects of children’s conditions including functional abilities (mobility, hand use, eating, and communication), 18 autonomic symptoms in six groups (cardiac, respiratory, sweating, temperature, gastrointestinal, and other), and parental stress. Bivariate and multivariable logistic regression analyses examined associations of dysautonomias with functional impairment, adjusted for type of DEE and age. Results: Of 313 participants with full information on function and dysautonomias, 156 (50%) were females. The median age was 8 years (interquartile range 4–12y); 255 (81%) participants had symptoms in at least one autonomic symptom group; 283 (90%) had impairment in at least one functional domain. The number of functional impairment domains and of autonomic symptom groups varied significantly across DEE groups (both p<0.001). The number of functional impairment domains and of autonomic symptom groups were correlated (Spearman’s r=0.35, p<0.001) on bivariate and multivariable analysis adjusted for DEE group and age. Parental stress was also independently correlated with dysautonomias (p<0.001). Interpretation: Parent-reported dysautonomias are common in children with DEEs. They correlate with extent of functional impairment and may contribute to caregiver stress. What this paper adds Dysautonomic symptoms are common in young people with developmental and epileptic encephalopathies (DEEs). Burden of dysautonomias is strongly correlated with burden of functional impairments. Aspects of dysautonomic function may provide biomarkers of DEE disease severity.
AB - Aim: To determine whether functional impairments and autonomic symptoms are correlated in young people with developmental and epileptic encephalopathies (DEEs). Method: Cross-sectional, online surveys (2018–2020) of parents recruited from family groups obtained information on several aspects of children’s conditions including functional abilities (mobility, hand use, eating, and communication), 18 autonomic symptoms in six groups (cardiac, respiratory, sweating, temperature, gastrointestinal, and other), and parental stress. Bivariate and multivariable logistic regression analyses examined associations of dysautonomias with functional impairment, adjusted for type of DEE and age. Results: Of 313 participants with full information on function and dysautonomias, 156 (50%) were females. The median age was 8 years (interquartile range 4–12y); 255 (81%) participants had symptoms in at least one autonomic symptom group; 283 (90%) had impairment in at least one functional domain. The number of functional impairment domains and of autonomic symptom groups varied significantly across DEE groups (both p<0.001). The number of functional impairment domains and of autonomic symptom groups were correlated (Spearman’s r=0.35, p<0.001) on bivariate and multivariable analysis adjusted for DEE group and age. Parental stress was also independently correlated with dysautonomias (p<0.001). Interpretation: Parent-reported dysautonomias are common in children with DEEs. They correlate with extent of functional impairment and may contribute to caregiver stress. What this paper adds Dysautonomic symptoms are common in young people with developmental and epileptic encephalopathies (DEEs). Burden of dysautonomias is strongly correlated with burden of functional impairments. Aspects of dysautonomic function may provide biomarkers of DEE disease severity.
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U2 - 10.1111/dmcn.14990
DO - 10.1111/dmcn.14990
M3 - Article
C2 - 34247387
AN - SCOPUS:85109400392
SN - 0012-1622
VL - 63
SP - 1433
EP - 1440
JO - Developmental Medicine and Child Neurology
JF - Developmental Medicine and Child Neurology
IS - 12
ER -