MRI-based quantification of ophthalmic changes in healthy volunteers during acute 15° head-down tilt as an analogue to microgravity

Spaceflight is known to cause ophthalmic changes in a condition known as spaceflight-associated neuro-ocular syndrome (SANS). It is hypothesized that SANS is caused by cephalad fluid shifts and potentially mild elevation of intracranial pressure (ICP) in microgravity. Head-down tilt (HDT) studies ar...

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Veröffentlicht in:Journal of the Royal Society interface 2021-04, Vol.18 (177), p.20200920-20200920, Article 20200920
Hauptverfasser: Sater, Stuart H, Sass, Austin M, Seiner, Akari, Natividad, Gabryel Conley, Shrestha, Dev, Fu, Audrey Q, Oshinski, John N, Ethier, C Ross, Martin, Bryn A
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Sprache:eng
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Zusammenfassung:Spaceflight is known to cause ophthalmic changes in a condition known as spaceflight-associated neuro-ocular syndrome (SANS). It is hypothesized that SANS is caused by cephalad fluid shifts and potentially mild elevation of intracranial pressure (ICP) in microgravity. Head-down tilt (HDT) studies are a ground-based spaceflight analogue to create cephalad fluid shifts. Here, we developed non-invasive magnetic resonance imaging (MRI)-based techniques to quantify ophthalmic structural changes under acute 15° HDT. We specifically quantified: (i) change in optic nerve sheath (ONS) and optic nerve (ON) cross-sectional area, (ii) change in ON deviation, an indicator of ON tortuosity, (iii) change in vitreous chamber depth, and (iv) an estimated ONS Young's modulus. Under acute HDT, ONS cross-sectional area increased by 4.04 mm (95% CI 2.88-5.21 mm , < 0. 000), while ON cross-sectional area remained nearly unchanged (95% CI -0.12 to 0.43 mm , = 0.271). ON deviation increased under HDT by 0.20 mm (95% CI 0.08-0.33 mm, = 0.002). Vitreous chamber depth decreased under HDT by -0.11 mm (95% CI -0.21 to -0.03 mm, = 0.009). ONS Young's modulus was estimated to be 85.0 kPa. We observed a significant effect of sex and BMI on ONS parameters, of interest since they are known risk factors for idiopathic intracranial hypertension. The tools developed herein will be useful for future analyses of ON changes in various conditions.
ISSN:1742-5662
1742-5689
1742-5662
DOI:10.1098/rsif.2020.0920