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. 2017 Nov 24;5(1):4-10.
doi: 10.1002/acn3.499. eCollection 2018 Jan.

Diagnostic Potential of Neural Exosome Cargo as Biomarkers for Acute Brain Injury

Laura Goetzl  1 , Nana Merabova  2 , Nune Darbinian  2 , Diana Martirosyan  2 , Erica Poletto  3 , Keri Fugarolas  4 , Ogechukwu Menkiti  4
Affiliations

Diagnostic Potential of Neural Exosome Cargo as Biomarkers for Acute Brain Injury

Laura Goetzl et al. Ann Clin Transl Neurol. .

Abstract

Objective: Neuronal exosomes purified from peripheral blood samples have been proposed as diagnostic tool in the setting of acute brain injury but never tested clinically. We hypothesized that exosome protein biomarkers would change over time following acute hypoxic brain injury and would predict response to therapy.

Methods: Synaptopodin (SYNPO), an actin-associated protein present in postsynaptic spines, was evaluated as a potential biomarker as well as: synaptophysin, neuron-specific enolase, and mitochondrial cytochrome c oxidase. A secondary analysis was performed on neonatal samples collected at 8, 10, and 14 h after the initiation of therapeutic-controlled hypothermia for acute hypoxic-ischemic encephalopathy (n = 14). Neuronal exosomes were purified from serum and protein levels were quantified using standard ELISA methods. The primary study outcomes were length of stay (LOS), discharge on seizure medication (DCMED), and composite neuroimaging score (NIS).

Results: The slope of change in neuronal exosome SYNPO between 8 and 14 h appeared to be the most promising biomarker for all three clinical study outcomes. SYNPO was highly correlated with LOS (-0.91, P < 0.001). SYNPO increased in 6/8 without DCMED and was worse or neutral in 5/5 with DCMED (P = 0.02). All four neonates with an abnormal NIS had neutral or decreasing SYNPO (P = 0.055). Other candidate biomarkers were not associated with outcomes.

Interpretation: This report provides the first clinical evidence that neural exosomes turn over rapidly enough in the peripheral circulation to be used as a "troponin-like" test following acute brain injury. Optimal sampling and biomarkers likely vary with type of brain injury.

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Figures

Figure 1
Figure 1
Nanoparticle‐tracking analysis of NNEs. Nanoparticle‐tracking analysis revealed a mean particle diameter of 134 nm ± 46.6 nm and a mode is 109.8 nm
Figure 2
Figure 2
Discharge on seizure medications. The slope of neural exosome and biomarkers levels between 8 and 14 h of controlled hypothermia or initial clinical biomarkers in patients requiring discharge on anticonvulsants compared to patients able to be discharged without medication. (A) Synaptopodin (SYNPO, P = 0.02), (B) neuronal‐specific enolase (NSE, P = 0.27)
Figure 3
Figure 3
Synaptopodin and Diffusion‐weighted Imaging Summary Score. The slope of neural exosome synaptopodin (SYNPO) levels between 8 and 14 h of controlled hypothermia and arithmetic sum of score from diffusion‐weighted images in basal ganglia and watershed (DS) (P = 0.055). Data not shown T1/T2 Summary Score, P = 0.15
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Grants and funding

This work was funded by Bill and Melinda Gates Foundation grant OPP1119489.

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