Neurological condition assessed with the Hempel examination and cognition and behaviour at 4years

To investigate associations between neurological condition, assessed with the Hempel examination, in terms of minor neurological dysfunction (MND) and neurological optimality, and cognition and behaviour at 4years. Cross-sectional analyses within a prospective, assessor-blinded follow-up study. Four...

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Published inEarly human development Vol. 112; pp. 9 - 13
Main Authors Schendelaar, Pamela, Seggers, Jorien, Heineman, Maas Jan, Hadders-Algra, Mijna
Format Journal Article
LanguageEnglish
Published Ireland Elsevier B.V 01.09.2017
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Abstract To investigate associations between neurological condition, assessed with the Hempel examination, in terms of minor neurological dysfunction (MND) and neurological optimality, and cognition and behaviour at 4years. Cross-sectional analyses within a prospective, assessor-blinded follow-up study. Four-year-old singletons born to subfertile parents (n=235; 120 boys). Outcome parameters were complex minor neurological dysfunction (complex MND) and the neurological optimality score (NOS). Cognitive outcome was evaluated with the Kaufman Assessment Battery for Children, resulting in a total intelligence quotient (IQ). Behavioural outcome was evaluated with the Child Behavior Checklist, resulting in a total problem T-score. Fifty-seven (24.3%) children had complex MND. None of the children showed fine motor dysfunction, suggesting a ceiling effect of the Hempel assessment. Complex MND was not correlated with IQ or total problem T-score. Nevertheless, a higher NOS was correlated with a higher IQ and a lower total problem T-score (adjusted mean estimate [95% confidence interval]: cognition: 0.445 [0.026; 0.865], p=0.038; behaviour: −0.458 [−0.830; −0.087], p=0.016). At age 4, complex MND assessed with the Hempel assessment was not associated with cognition and behaviour, presumably due to a ceiling effect in the Hempel domain of fine motor function. A more optimal neurological condition was associated with higher IQ and better behaviour. •At 4years, the Hempel assessment has a ceiling effect in fine motor function.•Complex MND determined with the Hempel assessment is not associated with cognition and behaviour in 4-year-olds.•Presumably, the tool of choice to assess MND in 4-year-olds is the MND-assessment rather than the Hempel assessment.•At age 4, the neurological optimality score was associated with cognition and behaviour.
AbstractList To investigate associations between neurological condition, assessed with the Hempel examination, in terms of minor neurological dysfunction (MND) and neurological optimality, and cognition and behaviour at 4years. Cross-sectional analyses within a prospective, assessor-blinded follow-up study. Four-year-old singletons born to subfertile parents (n=235; 120 boys). Outcome parameters were complex minor neurological dysfunction (complex MND) and the neurological optimality score (NOS). Cognitive outcome was evaluated with the Kaufman Assessment Battery for Children, resulting in a total intelligence quotient (IQ). Behavioural outcome was evaluated with the Child Behavior Checklist, resulting in a total problem T-score. Fifty-seven (24.3%) children had complex MND. None of the children showed fine motor dysfunction, suggesting a ceiling effect of the Hempel assessment. Complex MND was not correlated with IQ or total problem T-score. Nevertheless, a higher NOS was correlated with a higher IQ and a lower total problem T-score (adjusted mean estimate [95% confidence interval]: cognition: 0.445 [0.026; 0.865], p=0.038; behaviour: -0.458 [-0.830; -0.087], p=0.016). At age 4, complex MND assessed with the Hempel assessment was not associated with cognition and behaviour, presumably due to a ceiling effect in the Hempel domain of fine motor function. A more optimal neurological condition was associated with higher IQ and better behaviour.
AIMTo investigate associations between neurological condition, assessed with the Hempel examination, in terms of minor neurological dysfunction (MND) and neurological optimality, and cognition and behaviour at 4years.STUDY DESIGNCross-sectional analyses within a prospective, assessor-blinded follow-up study.SUBJECTSFour-year-old singletons born to subfertile parents (n=235; 120 boys).OUTCOME MEASURESOutcome parameters were complex minor neurological dysfunction (complex MND) and the neurological optimality score (NOS). Cognitive outcome was evaluated with the Kaufman Assessment Battery for Children, resulting in a total intelligence quotient (IQ). Behavioural outcome was evaluated with the Child Behavior Checklist, resulting in a total problem T-score.RESULTSFifty-seven (24.3%) children had complex MND. None of the children showed fine motor dysfunction, suggesting a ceiling effect of the Hempel assessment. Complex MND was not correlated with IQ or total problem T-score. Nevertheless, a higher NOS was correlated with a higher IQ and a lower total problem T-score (adjusted mean estimate [95% confidence interval]: cognition: 0.445 [0.026; 0.865], p=0.038; behaviour: -0.458 [-0.830; -0.087], p=0.016).INTERPRETATIONAt age 4, complex MND assessed with the Hempel assessment was not associated with cognition and behaviour, presumably due to a ceiling effect in the Hempel domain of fine motor function. A more optimal neurological condition was associated with higher IQ and better behaviour.
To investigate associations between neurological condition, assessed with the Hempel examination, in terms of minor neurological dysfunction (MND) and neurological optimality, and cognition and behaviour at 4years. Cross-sectional analyses within a prospective, assessor-blinded follow-up study. Four-year-old singletons born to subfertile parents (n=235; 120 boys). Outcome parameters were complex minor neurological dysfunction (complex MND) and the neurological optimality score (NOS). Cognitive outcome was evaluated with the Kaufman Assessment Battery for Children, resulting in a total intelligence quotient (IQ). Behavioural outcome was evaluated with the Child Behavior Checklist, resulting in a total problem T-score. Fifty-seven (24.3%) children had complex MND. None of the children showed fine motor dysfunction, suggesting a ceiling effect of the Hempel assessment. Complex MND was not correlated with IQ or total problem T-score. Nevertheless, a higher NOS was correlated with a higher IQ and a lower total problem T-score (adjusted mean estimate [95% confidence interval]: cognition: 0.445 [0.026; 0.865], p=0.038; behaviour: −0.458 [−0.830; −0.087], p=0.016). At age 4, complex MND assessed with the Hempel assessment was not associated with cognition and behaviour, presumably due to a ceiling effect in the Hempel domain of fine motor function. A more optimal neurological condition was associated with higher IQ and better behaviour. •At 4years, the Hempel assessment has a ceiling effect in fine motor function.•Complex MND determined with the Hempel assessment is not associated with cognition and behaviour in 4-year-olds.•Presumably, the tool of choice to assess MND in 4-year-olds is the MND-assessment rather than the Hempel assessment.•At age 4, the neurological optimality score was associated with cognition and behaviour.
Author Schendelaar, Pamela
Seggers, Jorien
Heineman, Maas Jan
Hadders-Algra, Mijna
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Keywords Neurological optimality score
Cognition
Behaviour
Preschool-age
Complex MND
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Snippet To investigate associations between neurological condition, assessed with the Hempel examination, in terms of minor neurological dysfunction (MND) and...
AIMTo investigate associations between neurological condition, assessed with the Hempel examination, in terms of minor neurological dysfunction (MND) and...
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pubmed
elsevier
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StartPage 9
SubjectTerms Behaviour
Child Behavior
Child, Preschool
Cognition
Complex MND
Female
Humans
Infant, Low Birth Weight - growth & development
Infant, Premature - growth & development
Male
Motor Skills
Neurological optimality score
Preschool-age
Title Neurological condition assessed with the Hempel examination and cognition and behaviour at 4years
URI https://dx.doi.org/10.1016/j.earlhumdev.2017.06.004
https://www.ncbi.nlm.nih.gov/pubmed/28645047
https://search.proquest.com/docview/1913396343
Volume 112
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