The relation of the multifocal electroretinographic response to macular layer volume.
The relation of the multifocal electroretinographic response to macular layer volume.
复制标题
多焦视网膜电图反应与黄斑层体积的关系。
DOI:
10.1007/s10633-022-09873-z
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发表时间:
2022
期刊:
影响因子:
--
通讯作者:
Akula,JamesD
中科院分区:
文献类型:
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作者:
Fonseca,MarianaI;Nouck-A-Nwal,Alexandra;Ambrosio,Lucia;Altschwager,Pablo;Hansen,RonaldM;Fulton,AnneB;Akula,JamesD
PurposeTo determine the association of the multifocal electroretinographic (mfERG) response amplitude with the volumes of theinner,postreceptor, andphotoreceptorretinal layers in the region stimulated by each mfERG element.MethodsSixteen healthy, young adult control subjects were studied. Each of the 103 hexagonal elements of the standard, scaled mfERG were aligned, where possible, with patches of retina imaged using optical coherence tomography. Stimuli falling on the fovea and on the optic nerve head were excluded. Linear mixed-effects modeling was then used to derive estimated coefficients (voltage/volume) for the mfERG response throughout the full 80 ms standard epoch. The resulting predicted response amplitudes originating in each layer were then compared to pharmacologically “dissected” mfERGs obtained from other studies in monkey eyes.ResultsAcross the duration of the response, the amplitude of the modeled contribution from (1) theinnerretina was small-to-modest, (2) thepostreceptorretina was larger and contained two prominent peaks, and (3) thephotoreceptorresponse was the largest and most closely paralleled the overall (i.e., intact) response, including late-appearing oscillations. The significance of each layer’s contribution was greatest when the absolute amplitude of that layer’s response was largest. The contribution of the inner retina was maximally significant in the intervalbetweenthe prominent troughs and peaks of the intact response. The contributions of the postreceptor and photoreceptor responses were maximally significantatthe prominent troughs and peaks of the intact response.ConclusionsThe results of the model were in good overall agreement with previous interpretations of the cellular contributions to the mfERG. There was also fair agreement with pharmacologically dissected monkey mfERG responses. Thus, the estimations of the contributions of the retinal layers to the mfERG so produced appeared plausible.