Neurofilament light chain: A potential biomarker for cerebrovascular disease in children with sickle cell anaemia

Author:

Green Nancy S.1ORCID,Rosano Caterina2,Bangirana Paul34,Opoka Robert5,Munube Deogratias5,Kasirye Philip5,Kawooya Michael67,Lubowa Samson K.6,Mupere Ezekiel5,Conroy Andrea8,Minja Frank J.9,Boehme Amelia K.10,Kang Min Suk10,Honig Lawrence S.10,Idro Richard5

Affiliation:

1. Department of Pediatrics Columbia University Irving Medical Center New York New York USA

2. Department of Epidemiology University of Pittsburgh Medical Center Pittsburgh Pennsylvania USA

3. Department of Psychiatry Makerere University College of Health Sciences Kampala Uganda

4. Global Health Uganda Kampala Uganda

5. Department of Paediatrics and Child Health Makerere University College of Health Sciences Kampala Uganda

6. Department of Radiology Makerere University College of Health Sciences Kampala Uganda

7. Ernest Cook Ultrasound Research and Education Institute (ECUREI) Mengo Hospital Kampala Uganda

8. Department of Pediatrics Indiana University School of Medicine Indianapolis Indiana USA

9. Department of Radiology and Imaging Sciences Emory University School of Medicine Atlanta Georgia USA

10. Department of Neurology Columbia University Irving Medical Center New York New York USA

Abstract

SummaryCerebrovascular injury frequently occurs in children with sickle cell anaemia (SCA). Limited access to magnetic resonance imaging and angiography (MRI‐MRA) in sub‐Saharan Africa impedes detection of clinically unapparent cerebrovascular injury. Blood‐based brain biomarkers of cerebral infarcts have been identified in non‐SCA adults. Using plasma samples from a well‐characterized cross‐sectional sample of Ugandan children with SCA, we explored relationships between biomarker levels and MRI‐detected cerebral infarcts and transcranial Doppler (TCD) arterial velocity. Testing was performed using a 4‐plex panel of brain injury biomarkers, including neurofilament light chain (NfL), a central nervous system neuron‐specific protein. Mean biomarker levels from the SCA group (n = 81) were similar to those from non‐SCA sibling controls (n = 54). Within the SCA group, NfL levels were significantly higher in those with MRI‐detected infarcts compared to no infarcts, and higher with elevated TCD velocity versus normal velocity. Elevated NfL remained strongly associated with MRI‐detected infarcts after adjusting for sex and age. All non‐SCA controls and SCA participants lacking MRI‐detected infarcts had low NfL levels. These data suggest potential utility of plasma‐based NfL levels to identify children with SCA cerebrovascular injury. Replication and prospective studies are needed to confirm these novel findings and the clinical utility of NfL versus MRI imaging.

Funder

Eunice Kennedy Shriver National Institute of Child Health and Human Development

Fogarty International Center

Publisher

Wiley

Subject

Hematology

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