TY - JOUR
T1 - Childhood motor difficulties and cognitive impairment in midlife: A 40-year cohort study
AU - Järvinen, Ilkka
AU - Schiavone, Nella
AU - Launes, Jyrki Tapani
AU - Lipsanen, Jari
AU - Virta, Maarit
AU - Vanninen, Ritva
AU - Lehto, Eliisa
AU - Tuulio-Henriksson, Annamari
AU - Hokkanen, Laura
N1 - Advance online publication.
PY - 2024/7/8
Y1 - 2024/7/8
N2 - Objective: We aimed to examine the association of childhood motor difficulties (MD) with cognitive impairment in midlife. Method: We studied 357 participants from a cohort born in 1971–1975. At age 9, they had completed the Test of Motor Impairment, which classified them into three groups: childhood MD (cMD), borderline cMD (bcMD), or no cMD. Participants with attention-deficit/hyperactivity disorder were excluded. At age 40, participants comprised 18 (5.0%) with cMD, 43 (12.0%) with bcMD, and 296 (82.9%) with no cMD. They underwent neuropsychological assessment covering six domains: executive functions, processing speed, attention and working memory, learning and memory, verbal symbolic abilities, and visuoperceptual and visuospatial abilities. A participant was considered to have an impairment if their performance was in the 15th percentile of a normative group. Results: Participants with cMD were more likely than those with no cMD to have an impairment in executive functions (OR = 6.73, p < .01), processing speed (OR = 3.85, p < .05), attention and working memory (OR = 4.79, p < .01), and a cross-domain impairment (OR = 3.62, p < .01). These differences remained significant after adjusting for parents’ occupation, sex, and low birth weight and after multiple imputation. No consistent difference emerged between participants with bcMD and no cMD. Conclusions: Childhood MD are associated with midlife cognitive impairment, which underscores their long-term implications. In the neuropsychological assessment of an adult patient, information on childhood motor development is of value. The assessment may help adapt the patient’s physical or occupational therapy to the patient’s cognitive profile.
AB - Objective: We aimed to examine the association of childhood motor difficulties (MD) with cognitive impairment in midlife. Method: We studied 357 participants from a cohort born in 1971–1975. At age 9, they had completed the Test of Motor Impairment, which classified them into three groups: childhood MD (cMD), borderline cMD (bcMD), or no cMD. Participants with attention-deficit/hyperactivity disorder were excluded. At age 40, participants comprised 18 (5.0%) with cMD, 43 (12.0%) with bcMD, and 296 (82.9%) with no cMD. They underwent neuropsychological assessment covering six domains: executive functions, processing speed, attention and working memory, learning and memory, verbal symbolic abilities, and visuoperceptual and visuospatial abilities. A participant was considered to have an impairment if their performance was in the 15th percentile of a normative group. Results: Participants with cMD were more likely than those with no cMD to have an impairment in executive functions (OR = 6.73, p < .01), processing speed (OR = 3.85, p < .05), attention and working memory (OR = 4.79, p < .01), and a cross-domain impairment (OR = 3.62, p < .01). These differences remained significant after adjusting for parents’ occupation, sex, and low birth weight and after multiple imputation. No consistent difference emerged between participants with bcMD and no cMD. Conclusions: Childhood MD are associated with midlife cognitive impairment, which underscores their long-term implications. In the neuropsychological assessment of an adult patient, information on childhood motor development is of value. The assessment may help adapt the patient’s physical or occupational therapy to the patient’s cognitive profile.
KW - 515 Psychology
KW - childhood motor difficulties
KW - developmental coordination disorder
KW - cognitive impairment
KW - cohort study
U2 - 10.1037/neu0000961
DO - 10.1037/neu0000961
M3 - Article
SN - 0894-4105
VL - 38
SP - 501
EP - 515
JO - Neuropsychology
JF - Neuropsychology
IS - 6
ER -