Comparisons Among Optical Coherence Tomography and Fundus Autofluorescence Modalities as Measurements of Atrophy in ABCA4-Associated Disease.

Comparisons Among Optical Coherence Tomography and Fundus Autofluorescence Modalities as Measurements of Atrophy in ABCA4-Associated Disease.
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DOI:
10.1167/tvst.11.1.36
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发表时间:
2022-01-03
影响因子:
3
通讯作者:
Sparrow JR
Sparrow JR
中科院分区:
医学3区
文献类型:
--
作者:
Parmann R;Tsang SH;Zernant J;Allikmets R;Greenstein VC;Sparrow JR

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在ABCA 4相关视网膜病变中,通过光谱域光学相干断层扫描(SD-OCT)以及短波长(SW-AF)和近红外(NIR-AF)自体荧光评估中心萎缩。患者表现出中央萎缩性病变,其特征为两个AF图像中的低自体荧光(hypoAF)被高自体荧光(hyperAF)环包围(第1组,4例患者);或SW-AF中的hyperAF环,但在NIR-AF图像中没有(第2组,11例患者);或两个AF图像中的hyperAF环(第3组,11例患者)。在中央凹SD-OCT扫描中测量脉络膜过度透射和椭圆区(EZ)丢失宽度,在AF图像中,沿同一轴沿着测量hypo+hyperAF宽度。采用Bland-Altman和重复测量方差分析及Tukey事后分析。对于所有组,超传输宽度显着小于EZ损失宽度。在组1和组2中,超透射宽度与SW-hypoAF宽度无显著差异,但超透射宽度窄于SW-hypo +hyperAF(组1,2)和NIR-hypo +hyperAF(组1)的宽度。在第3组中,超透射宽度也显著小于SW-hypoAF和NIR-hypoAF的宽度。EZ损失宽度与总病变大小的测量值无显著差异,后者是SW-低+高AF和NIR-低+高AF的宽度(第1组); NIR-低AF和SW-低+高AF的宽度(第2组);以及NIR-低AF和SW-低AF的宽度(第3组)。超透射和SW-hypoAF(除非反映总病变宽度)低估了EZ丢失、SW-hypoAF +hyperAF和NIR-hypo +hyperAF检测到的病变大小。研究结果对临床研究中结局指标的选择具有重要意义。
In ABCA4-associated retinopathy, central atrophy was assessed by spectral domain optical coherence tomography (SD-OCT) and by short-wavelength (SW-AF) and near-infrared (NIR-AF) autofluorescence. Patients exhibited a central atrophic lesion characterized by hypoautofluorescence (hypoAF) surrounded either by hyperautofluorescent (hyperAF) rings in both AF images (group 1, 4 patients); or a hyperAF ring in SW-AF but not in NIR-AF images (group 2, 11 patients); or hyperAF rings in neither AF images (group 3, 11 patients). Choroidal hypertransmission and widths of ellipsoid zone (EZ) loss were measured in foveal SD-OCT scans, and in AF images hypoAF and total hypo+hyperAF widths were measured along the same axis. Bland-Altman and repeated measures analysis of variance with Tukey post hoc were applied. For all groups, hypertransmission widths were significantly smaller than EZ loss widths. In Groups 1 and 2, hypertransmission width was not significantly different than SW-hypoAF width, but hypertransmission was narrower than the width of SW-hypo+hyperAF (groups 1, 2) and NIR-hypo+hyperAF (group 1). In group 3, the hypertransmission width was also significantly less than the width of SW-hypoAF and NIR-hypoAF. The EZ loss widths were not significantly different than measurements of total lesion size, the latter being the widths of SW-hypo+hyperAF and NIR-hypo+hyperAF (group 1); widths of NIR-hypoAF and SW-hypo+hyperAF (group 2); and widths of NIR-hypoAF and SW-hypoAF (group 3). Hypertransmission and SW-hypoAF (except when reflecting total lesion width) underestimate lesion size detected by EZ loss, SW-hypoAF+hyperAF, and NIR-hypo+hyperAF. The findings are significant to the selection of outcome measures in clinical studies.
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