Optic disc edema during strict 6° head-down tilt bed rest is related to one-carbon metabolism pathway genetics and optic cup volume

Sara R. Zwart, Brandon R. Macias, Steven S. Laurie, Connor Ferguson, Claudia Stern, Alex Suh, M. Mark Melin, Millennia Young, Eric Bershad, Scott M. Smith
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Abstract

Some astronauts on International Space Station missions experience neuroophthalmological pathologies as part of spaceflight associated neuro-ocular syndrome (SANS). Strict head-down tilt bed rest (HDTBR) is a spaceflight analog that replicates SANS findings and those who had 3–4 risk alleles (G and C alleles from the methionine synthase reductase [MTRR] A66G and serine hydroxymethyltransferase [SHMT1] C1420T, respectively) as compared to 1-2 risk alleles, had a greater increase in total retinal thickness (TRT). The objective of this study was to identify factors that contribute to the individual variability of the development of SANS in a 60 d HDTBR at the German Aerospace Center’s:envihab facility, Cologne Germany. 22 of 24 subjects who participated in the HDTBR study provided blood samples for genetic analysis. Total retinal thickness and optic cup volume were measured before and after bed rest. Subjects with 3–4 versus 0-2 risk alleles had greater ΔTRT during and after bed rest, and the model improved with the addition of baseline optic cup volume. This bed rest study confirms that variants of MTRR and SHMT1 are associated with ocular pathologies. Subjects with more risk alleles had the greatest HDTBR-induced ΔTRT, reaffirming that genetics predispose some individuals to developing SANS. Preflight optic cup volume and genetics better predict ΔTRT than either one alone. Whether nutritional supplements can override the genetic influences on biochemistry, physiology, and pathophysiology remains to be tested. These findings have significant implications for both aerospace and terrestrial medicine.
严格6°倒立卧床时视盘水肿与单碳代谢途径遗传和视杯容积有关
一些参加国际空间站任务的宇航员会出现神经眼病理,这是航天相关神经眼综合征(SANS)的一部分。严格的头下倾斜卧床(HDTBR)是重复SANS研究结果的航天模拟实验,与1-2个风险等位基因相比,携带3-4个风险等位基因(分别来自蛋氨酸合酶还原酶[MTRR] A66G和丝氨酸羟甲基转移酶[SHMT1] C1420T的G和C等位基因)的患者视网膜总厚度(TRT)增加更大。本研究的目的是在德国科隆的德国航空航天中心:envihab设施进行的60天HDTBR研究中,确定导致SANS发展个体差异的因素。参与HDTBR研究的24名受试者中有22名提供了血液样本用于遗传分析。测定卧床休息前后视网膜总厚度和视杯体积。有3-4个风险等位基因的受试者与0-2个风险等位基因的受试者在卧床休息期间和之后有更大的ΔTRT,并且模型随着基线视杯体积的增加而改进。这项卧床休息研究证实MTRR和SHMT1的变异与眼部病变有关。具有更多风险等位基因的受试者具有最大的hdtbr诱导ΔTRT,重申遗传使某些个体易患SANS。飞行前视杯体积和基因比单独一个更能预测ΔTRT。营养补充剂是否能克服遗传对生物化学、生理学和病理生理学的影响还有待检验。这些发现对航空航天和地面医学都具有重要意义。
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