Ipsilesional volume loss of basal ganglia and thalamus is associated with poor hand function after ischemic perinatal stroke.


Journal

BMC neurology
ISSN: 1471-2377
Titre abrégé: BMC Neurol
Pays: England
ID NLM: 100968555

Informations de publication

Date de publication:
12 Jan 2022
Historique:
received: 19 05 2021
accepted: 28 12 2021
entrez: 13 1 2022
pubmed: 14 1 2022
medline: 15 1 2022
Statut: epublish

Résumé

Perinatal stroke (PS) is the leading cause of hemiparetic cerebral palsy (CP). Involvement of the corticospinal tract on neonatal magnetic resonance imaging (MRI) is predictive of motor outcome in patients with hemiparetic CP. However, early MRI is not available in patients with delayed presentation of PS and prediction of hemiparesis severity remains a challenge. To evaluate the volumes of the basal ganglia, amygdala, thalamus, and hippocampus following perinatal ischemic stroke in relation to hand motor function in children with a history of PS and to compare the volumes of subcortical structures in children with PS and in healthy controls. Term born PS children with arterial ischemic stroke (AIS) (n = 16) and with periventricular venous infarction (PVI) (n = 18) were recruited from the Estonian Pediatric Stroke Database. MRI was accuired during childhood (4-18 years) and the volumes of the basal ganglia, thalamus, amygdala and hippocampus were calculated. The results of stroke patients were compared to the results of 42 age- and sex-matched healthy controls. Affected hand function was evaluated by Assisting Hand Assessment (AHA) and classified by the Manual Ability Classification System (MACS). Compared to the control group, children with AIS had smaller volumes of the ipsi- and contralesional thalami, ipsilesional globus pallidus, nucleus accumbens and hippocampus (p < 0.005). Affected hand function in children with AIS was correlated with smaller ipsilesional thalamus, putamen, globus pallidus, hippocampus, amygdala and contralesional amygdala (r > 0.5; p < 0.05) and larger volume of the contralesional putamen and hippocampus (r < - 0.5; p < 0.05). In children with PVI, size of the ipsilesional caudate nucleus, globus pallidus, thalamus (p ≤ 0.001) and hippocampus (p < 0.03) was smaller compared to controls. Smaller volume of the ipsi- and contralesional thalami and ipsilesional caudate nucleus was correlated with affected hand function (r > 0.55; p < 0.05) in children with PVI. Smaller volume of ipsilesional thalamus was associated with poor affected hand function regardless of the perinatal stroke subtype. The pattern of correlation between hand function and volume differences in the other subcortical structures varied between children with PVI and AIS. Evaluation of subcortical structures is important in predicting motor outcome following perinatal stroke.

Sections du résumé

BACKGROUND BACKGROUND
Perinatal stroke (PS) is the leading cause of hemiparetic cerebral palsy (CP). Involvement of the corticospinal tract on neonatal magnetic resonance imaging (MRI) is predictive of motor outcome in patients with hemiparetic CP. However, early MRI is not available in patients with delayed presentation of PS and prediction of hemiparesis severity remains a challenge.
AIMS OBJECTIVE
To evaluate the volumes of the basal ganglia, amygdala, thalamus, and hippocampus following perinatal ischemic stroke in relation to hand motor function in children with a history of PS and to compare the volumes of subcortical structures in children with PS and in healthy controls.
METHODS METHODS
Term born PS children with arterial ischemic stroke (AIS) (n = 16) and with periventricular venous infarction (PVI) (n = 18) were recruited from the Estonian Pediatric Stroke Database. MRI was accuired during childhood (4-18 years) and the volumes of the basal ganglia, thalamus, amygdala and hippocampus were calculated. The results of stroke patients were compared to the results of 42 age- and sex-matched healthy controls. Affected hand function was evaluated by Assisting Hand Assessment (AHA) and classified by the Manual Ability Classification System (MACS).
RESULTS RESULTS
Compared to the control group, children with AIS had smaller volumes of the ipsi- and contralesional thalami, ipsilesional globus pallidus, nucleus accumbens and hippocampus (p < 0.005). Affected hand function in children with AIS was correlated with smaller ipsilesional thalamus, putamen, globus pallidus, hippocampus, amygdala and contralesional amygdala (r > 0.5; p < 0.05) and larger volume of the contralesional putamen and hippocampus (r < - 0.5; p < 0.05). In children with PVI, size of the ipsilesional caudate nucleus, globus pallidus, thalamus (p ≤ 0.001) and hippocampus (p < 0.03) was smaller compared to controls. Smaller volume of the ipsi- and contralesional thalami and ipsilesional caudate nucleus was correlated with affected hand function (r > 0.55; p < 0.05) in children with PVI.
CONCLUSIONS CONCLUSIONS
Smaller volume of ipsilesional thalamus was associated with poor affected hand function regardless of the perinatal stroke subtype. The pattern of correlation between hand function and volume differences in the other subcortical structures varied between children with PVI and AIS. Evaluation of subcortical structures is important in predicting motor outcome following perinatal stroke.

Identifiants

pubmed: 35022000
doi: 10.1186/s12883-022-02550-3
pii: 10.1186/s12883-022-02550-3
pmc: PMC8753896
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

23

Informations de copyright

© 2022. The Author(s).

Références

Res Dev Disabil. 2020 Feb;97:103569
pubmed: 31901671
Neurosci Biobehav Rev. 2007;31(8):1136-49
pubmed: 18053875
Dev Med Child Neurol. 2010 Feb;52(2):145-52
pubmed: 19807768
Semin Perinatol. 2015 Mar;39(2):141-6
pubmed: 25813668
Stroke. 2013 Nov;44(11):3265-71
pubmed: 24105698
Neurorehabil Neural Repair. 2013 Jan;27(1):72-8
pubmed: 22677505
J Child Neurol. 2016 Apr;31(5):621-8
pubmed: 26446909
Int J Stroke. 2016 Dec;11(9):1028-1035
pubmed: 27550558
Neuroimage. 2011 Jun 1;56(3):907-22
pubmed: 21352927
Brain. 2007 Sep;130(Pt 9):2375-86
pubmed: 17698497
Pediatrics. 2010 Oct;126(4):912-8
pubmed: 20855393
Neuroimage Clin. 2019;21:101660
pubmed: 30639178
Epilepsia Open. 2018 Mar 02;3(2):193-202
pubmed: 29881798
Stroke. 2019 Mar;50(3):e51-e96
pubmed: 30686119
Neurosci Biobehav Rev. 2007;31(8):1150-6
pubmed: 17624432
Pediatrics. 2005 Feb;115(2):321-6
pubmed: 15687439
Eur J Paediatr Neurol. 2018 Nov;22(6):1006-1015
pubmed: 30249407
Eur J Paediatr Neurol. 2010 Mar;14(2):169-77
pubmed: 19272822
Eur J Paediatr Neurol. 2020 Mar;25:97-105
pubmed: 31740218
Stroke. 2007 Aug;38(8):2234-40
pubmed: 17585082
Dev Med Child Neurol. 2006 Jul;48(7):549-54
pubmed: 16780622
Arch Neurol. 2010 Jul;67(7):842-8
pubmed: 20625091
Dev Med Child Neurol. 2000 Dec;42(12):816-24
pubmed: 11132255
Brain Dev. 2016 Mar;38(3):267-73
pubmed: 26428444
Stroke. 2018 Apr;49(4):931-937
pubmed: 29523650
Dev Med Child Neurol. 2010 Apr;52(4):352-7
pubmed: 19583744
Neuropediatrics. 2005 Feb;36(1):12-20
pubmed: 15776318
Neuroimage. 2001 Jul;14(1 Pt 1):21-36
pubmed: 11525331
Neuroimage. 2002 Sep;17(1):479-89
pubmed: 12482100
Hum Brain Mapp. 2015 Dec;36(12):4793-807
pubmed: 26512551
Acta Paediatr. 2009 Nov;98(11):1720-6
pubmed: 19673723
Neuroimage Clin. 2019;21:101670
pubmed: 30642756
Pediatrics. 2007 Sep;120(3):609-16
pubmed: 17766535
Stroke. 2016 Jun;47(6):1647-50
pubmed: 27165960
Stroke. 2012 Jun;43(6):1602-8
pubmed: 22474056
Pediatrics. 1999 Jan;103(1):39-46
pubmed: 9917437
Pediatr Neurol. 2019 Nov;100:49-54
pubmed: 31147227
Dev Med Child Neurol. 2020 Apr;62(4):513-520
pubmed: 31489622
Eur J Neurol. 2017 Aug;24(8):1006-1015
pubmed: 28646492
Ann Neurol. 2008 Apr;63(4):436-43
pubmed: 18306227
Pediatr Neurol. 2009 Mar;40(3):205-14
pubmed: 19218034
Lancet Child Adolesc Health. 2018 Sep;2(9):666-676
pubmed: 30119760
J Clin Epidemiol. 2014 Aug;67(8):850-7
pubmed: 24831050
J Neurol Sci. 1995 Dec;134(1-2):130-5
pubmed: 8747855

Auteurs

Nigul Ilves (N)

Radiology Clinic, Tartu University Hospital, Tartu, Estonia. Nigul.ilves@kliinikum.ee.
Department of Radiology, University of Tartu, L. Puusepa 8, 51014, Tartu, Estonia. Nigul.ilves@kliinikum.ee.

Silva Lõo (S)

Department of Pediatric Neurology, University of Helsinki; Helsinki University Hospital, Helsinki, Finland.
Department of Pediatrics, University of Tartu, Tartu, Estonia.

Norman Ilves (N)

Radiology Clinic, Tartu University Hospital, Tartu, Estonia.
Department of Radiology, University of Tartu, L. Puusepa 8, 51014, Tartu, Estonia.

Rael Laugesaar (R)

Department of Pediatrics, University of Tartu, Tartu, Estonia.
Children's Clinic, Tartu University Hospital, Tartu, Estonia.

Dagmar Loorits (D)

Radiology Clinic, Tartu University Hospital, Tartu, Estonia.

Pille Kool (P)

Department of Radiology, University of Tartu, L. Puusepa 8, 51014, Tartu, Estonia.

Tiina Talvik (T)

Children's Clinic, Tartu University Hospital, Tartu, Estonia.

Pilvi Ilves (P)

Radiology Clinic, Tartu University Hospital, Tartu, Estonia.
Department of Radiology, University of Tartu, L. Puusepa 8, 51014, Tartu, Estonia.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH