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Hypertransmission as a biomarker for predicting postoperative microstructure and function of idiopathic macular hole
Huifang Yue1, Yuexin Shi2, Zeqi Fan1
1Shanxi Eye Hospital, Shanxi, China.
Purpose:
To observe choroidal hypertransmission in idiopathic macular hole (IMH) before and after surgery using spectral-domain optical coherence tomography (SD-OCT), and to assess its correlation with retinal microstructure and visual outcomes to determine whether hypertransmission can serve as a biomarker for predicting IMH prognosis.
Methods:
This retrospective, observational study included patients diagnosed with IMH at Shanxi Eye Hospital between January 2019 and December 2020, who successfully achieved hole closure after vitrectomy, and had complete follow-up data. SD-OCT was used to assess baseline and postoperative retinal structures, and best-corrected visual acuity (BCVA) was recorded. The follow-up time was 3-52 months.
Results:
Fifty-four eyes (53 patients) were enrolled. On preoperative SD-OCT, 41 eyes (75.9 %) showed hypertransmission, with no differences in duration, MH stage, base diameter, pre- and postoperative BCVA, or restoration of the external limiting membrane (ELM) and ellipsoid zone (EZ) between patients with and without preoperative hypertransmission (p > 0.05). With or without hypertransmission on postoperative SD-OCT were 17 and 37 eyes showed significant differences in duration (p = 0.001), base diameter (p = 0.001), and baseline BCVA (p = 0.029), as well as in the intraoperative inner limiting membrane procedure (p = 0.012) and tamponade (p = 0.021). Multivariate regression analysis showed that only base diameter was associated with postoperative hypertransmission (p = 0.024, odds ratio [OR] = 1.004, 95 %CI 1.001-1.008). The ELM (17/20) and EZ (17/51) lines in 17 eyes with postoperative hypertransmission were not restored at the final follow-up.
Conclusions:
Larger base diameter, poorer retinal microstructure, and visual acuity were associated with postoperative hypertransmission, indicating its potential as a biomarker for poor prognosis in patients with IMH.
