Journal of Otolaryngology and Ophthalmology of Shandong University ›› 2020, Vol. 34 ›› Issue (4): 69-74.doi: 10.6040/j.issn.1673-3770.1.2020.046

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Measurement of the parameters of the macular retinal and peripapillary vasculature in neuromyelitis optica spectrum disorder patientsXU Jing, QU Yuanzhen, LIANG Xiaofang, YANG Liu, TANG Yang Department of Ophthalmology,Beijing Tiantan Hospital, Capital Medical University, Beijing 100070, ChinaAbstract: Objective〓

To evaluate the changes in the parameters of the macular and peripapillary vasculature in patients with neuromyelitis optica spectrum disorder(NMOSD). MethodsThis case-control study involved 40(76 eyes)aquaporin-4 antibody-positive NMOSD patients and 40(80 eyes)age- and gender-matched healthy controls(HCs). Of 76 eyes with NMOSD, 34 had a history of optic neuritis(ON); 40 had no history of ON. Macular superficial vessel density(MSVD), macular deep vessel density(MDVD), and radial peripapillary capillary(RPC)density were measured by OCT-A. The retinal nerve fiber layer(RNFL)and ganglion cell complex(GCC)thicknesses were measured by OCT. Comparisons of the retinal structural and microvascular parameters of the cohorts were performed using generalized estimating equation(GEE)models. The relationship between retinal vessel density and retinal thickness was also analyzed. ResultsRPC density and MSVD were significantly lower in eyes with NMOSD+ON than in those with NMOSD-ON and HC(P<0.05). The GCC and RNFL thicknesses were also significantly thinner in eyes with NMOSD+ON than in those with NMOSD-ON and HC(P<0.001 for both). MDVD was lower in eyes with NMOSD-ON than in those with HC(P<0.05); however, other vessel densities were not significantly different(P>0.05). In eyes with NMOSD, MSVD, whole image vessel density(WIVD)of RPC, and peripapillary vessel density(PPVD)were correlated with GCC and RNFL thicknesses(P<0.001). However, MDVD and inside disc vessel density(IDVD)were not correlated with GCC and RNFL thicknesses(P>0.05). ConclusionRetinal microvascular changes were present in eyes with NMOSD+ON. However, these changes, except those in MDVD, were not significant in eyes with NMOSD-ON. Thinner GCC and RNFL were associated with lower MSVD and RPC density.   

  1. Key words:Neuromyelitis optica spectrum disorder;
    Optic neuritis;
    Tomography, optical coherence;
    Angiography;
    Vessel density视神经脊髓炎谱系疾病(Neuromyelitis optica spectrum disorder, NMOSD)是一种视神经与脊髓相继或同时受累的自身免疫性脱髓鞘性疾病[1-2], 占亚洲人群脱髓鞘疾病的20%~48%[3], 水通道蛋白4抗体(aquaporin4-antibody, AQP4-Ab)是其特异性指标[4], 可在60%~80%的NMOSD患者中检测到, 使我们对该疾病的免疫发病机制的理解得以迅速发展[5]。NMOSD患者中约50%以视神经炎(optic neuritis, ON)为首发表现, 其中大约50%表现为孤立的视神经炎, 持续且严重的视力损伤是NMO视神经炎的特征表现[1, 6]。然而, ON在NMOSD第一次发作的时间因患者而异, 在第一次发作之前眼底很少有明显的形态学改变。在临床NMOSD症状出现之前, 亚临床疾病活动通常不明显。在本研究中, 我们使用相干光层析成像术(optical coherence tomography, OCT)和相干光层析血管成像术(optical coherence tomography angiography, OCT-A)对AQP4-Ab阳性的NMOSD患者眼和正常人群眼的黄斑、视乳头血管情况进行对照研究, 以探索NMOSD的视网膜结构和微血管损伤以及两者之间关系。
  • Received:2020-05-22 Online:2020-07-20 Published:2020-08-28

Abstract: Objective To evaluate the changes in the parameters of the macular and peripapillary vasculature in patients with neuromyelitis optica spectrum disorder(NMOSD). Methods This case-control study involved 40(76 eyes)aquaporin-4 antibody-positive NMOSD patients and 40(80 eyes)age- and gender-matched healthy controls(HCs). Of 76 eyes with NMOSD, 34 had a history of optic neuritis(ON); 40 had no history of ON. Macular superficial vessel density(MSVD), macular deep vessel density(MDVD), and radial peripapillary capillary(RPC)density were measured by OCT-A. The retinal nerve fiber layer(RNFL)and ganglion cell complex(GCC)thicknesses were measured by OCT. Comparisons of the retinal structural and microvascular parameters of the cohorts were performed using generalized estimating equation(GEE)models. The relationship between retinal vessel density and retinal thickness was also analyzed. Results RPC density and MSVD were significantly lower in eyes with NMOSD+ON than in those with NMOSD-ON and HC(P<0.05). The GCC and RNFL thicknesses were also significantly thinner in eyes with NMOSD+ON than in those with NMOSD-ON and HC(P<0.001 for both). MDVD was lower in eyes with NMOSD-ON than in those with HC(P<0.05); however, other vessel densities were not significantly different(P>0.05). In eyes with NMOSD, MSVD, whole image vessel density(WIVD)of RPC, and peripapillary vessel density(PPVD)were correlated with GCC and RNFL thicknesses(P<0.001). However, MDVD and inside disc vessel density(IDVD)were not correlated with GCC and RNFL thicknesses(P>0.05). Conclusion Retinal microvascular changes were present in eyes with NMOSD+ON. However, these changes, except those in MDVD, were not significant in eyes with NMOSD-ON. Thinner GCC and RNFL were associated with lower MSVD and RPC density.

Key words: Neuromyelitis optica spectrum disorder, Optic neuritis, Tomography, optical coherence, Angiography, Vessel density

CLC Number: 

  • R774.6+1
[1] Jarius S, Wildemann B, Paul F. Neuromyelitis optica: clinical features, immunopathogenesis and treatment[J]. Clin Exp Immunol, 2014, 176(2): 149-164. doi:10.1111/cei.12271.
[2] 中国免疫学会神经免疫学分会, 中华医学会神经病学分会神经免疫学组, 中国医师协会神经内科分会神经免疫专业委员会. 中国视神经脊髓炎谱系疾病诊断与治疗指南[J].中国神经免疫学和神经病学杂志, 2016,23(3): 155-166. doi:10.3969/j.issn.1006-2963.2016.03.001.
[3] Levin MH, Bennett JL, Verkman AS. Optic neuritis in neuromyelitis optica[J]. Prog Retin Eye Res, 2013, 36: 159-171. doi:10.1016/j.preteyeres.2013.03.001.
[4] Wingerchuk DM, Lennon VA, Lucchinetti CF, et al. The spectrum of neuromyelitis optica[J]. Lancet Neurol, 2007, 6(9): 805-815. doi:10.1016/s1474-4422(07)70216-8.
[5] Metz I, Beiβbarth T, Ellenberger D, et al. Serum peptide reactivities may distinguish neuromyelitis optica subgroups and multiple sclerosis[J]. Neurol Neuroimmunol Neuroinflamm, 2016, 3(2): e204. doi:10.1212/NXI.0000000000000204.
[6] Petzold A, Plant GT. Diagnosis and classification of autoimmune optic neuropathy[J]. Autoimmun Rev, 2014, 13(4/5): 539-545. doi:10.1016/j.autrev.2014.01.009.
[7] Wingerchuk DM, Banwell B, Bennett JL, et al. International consensus diagnostic criteria for neuromyelitis optica spectrum disorders[J]. Neurology, 2015, 85(2): 177-189. doi:10.1212/WNL.0000000000001729.
[8] The clinical profile of optic neuritis. Experience of the optic neuritis treatment trial. Optic neuritis study group[J]. Arch Ophthalmol, 1991, 109(12): 1673-1678. doi:10.1001/archopht.1991.01080120057025.
[9] Augstburger E, Zéboulon P, Keilani C, et al. Retinal and choroidal microvasculature in nonarteritic anterior ischemic optic neuropathy: an optical coherence tomography angiography study[J]. Invest Ophthalmol Vis Sci, 2018, 59(2): 870-877. doi:10.1167/iovs.17-22996.
[10] Zonta M, Angulo MC, Gobbo S, et al. Neuron-to-astrocyte signaling is central to the dynamic control of brain microcirculation[J]. Nat Neurosci, 2003, 6(1): 43-50. doi:10.1038/nn980.
[11] Felix CM, Levin MH, Verkman AS. Complement-independent retinal pathology produced by intravitreal injection of neuromyelitis optica immunoglobulin G[J]. J Neuroinflammation, 2016, 13(1): 275. doi:10.1186/s12974-016-0746-9.
[12] Green AJ, Cree BA. Distinctive retinal nerve fibre layer and vascular changes in neuromyelitis optica following optic neuritis[J]. J Neurol Neurosurg Psychiatry, 2009, 80(9): 1002-1005. doi:10.1136/jnnp.2008.166207.
[13] 成璐, 董田田, 凌振芬. 视乳头血流改变在视神经脊髓炎疾病进展评估中的作用[J].中国临床神经科学, 2018, 26(2): 32-38+63. CHENG Lu, DONG Tiantian, LING Zhengfeng. Evaluation of Neuromyelitis Optica Patients through Optic Nerve Head Blood Flow Density[J]. Chinese Journal of Clinical Neurosciences, 2018,26(2): 32-38+63.
[14] Kwapong WR, Peng CL, He ZY, et al. Altered macular microvasculature in neuromyelitis optica spectrum disorders[J]. Am J Ophthalmol, 2018, 192: 47-55. doi:10.1016/j.ajo.2018.04.026.
[15] Kwapong WR, Yan JY, Xie LF, et al. Retinal microvasculature alterations in neuromyelitis optica spectrum disorders before optic neuritis[J]. Mult Scler Relat Disord, 2020, 44: 102277. doi:10.1016/j.msard.2020.102277.
[16] Roemer SF, Parisi JE, Lennon VA, et al. Pattern-specific loss of aquaporin-4 immunoreactivity distinguishes neuromyelitis optica from multiple sclerosis[J]. Brain, 2007, 130(Pt 5): 1194-1205. doi:10.1093/brain/awl371.
[17] Jiang H, Gameiro GR, Liu Y, et al. Visual function and disability are associated with increased retinal volumetric vessel density in patients with multiple sclerosis[J]. Am J Ophthalmol, 2020, 213: 34-45. doi:10.1016/j.ajo.2019.12.021.
[18] Chen YH, Shi C, Zhou LL, et al. Corrigendum: the detection of Retina microvascular density in subclinical aquaporin-4 antibody seropositive neuromyelitis optica spectrum disorders[J]. Front Neurol, 2020, 11: 217. doi:10.3389/fneur.2020.00217.
[19] Huang YH, Zhou L, ZhangBao JZ, et al. Peripapillary and parafoveal vascular network assessment by optical coherence tomography angiography in aquaporin-4 antibody-positive neuromyelitis optica spectrum disorders[J]. Br J Ophthalmol, 2019, 103(6): 789-796. doi:10.1136/bjophthalmol-2018-312231.
[20] You YY, Zhu L, Zhang T, et al. Evidence of Müller glial dysfunction in patients with aquaporin-4 immunoglobulin G-positive neuromyelitis optica spectrum disorder[J]. Ophthalmology, 2019, 126(6): 801-810. doi:10.1016/j.ophtha.2019.01.016.
[21] Yu J, Gu RP, Zong Y, et al. Relationship between retinal perfusion and retinal thickness in healthy subjects: an optical coherence tomography angiography study[J]. Invest Ophthalmol Vis Sci, 2016, 57(9): OCT204-OCT210. doi:10.1167/iovs.15-18630.
[22] Oertel FC, Kuchling J, Zimmermann H, et al. Microstructural visual system changes in AQP4-antibody-seropositive NMOSD[J]. Neurol Neuroimmunol Neuroinflamm, 2017, 4(3): e334. doi:10.1212/NXI.0000000000000334.
[23] Jeong IH, Kim HJ, Kim NH, et al. Subclinical primary retinal pathology in neuromyelitis optica spectrum disorder[J]. J Neurol, 2016, 263(7): 1343-1348. doi:10.1007/s00415-016-8138-8.
[24] Bennett JL, de Seze J, Lana-Peixoto M, et al. Neuromyelitis optica and multiple sclerosis: Seeing differences through optical coherence tomography[J]. Mult Scler, 2015, 21(6): 678-688. doi:10.1177/1352458514567216.
[25] Zhao XJ, Qiu W, Zhang YX, et al. A prospective case-control study comparing optical coherence tomography characteristics in neuromyelitis optica spectrum disorder- optic neuritis and idiopathic optic neuritis[J]. BMC Ophthalmol, 2018, 18(1): 247. doi:10.1186/s12886-018-0902-3.
[26] Mateo J, Esteban O, Martínez M, et al. The contribution of optical coherence tomography in neuromyelitis optica spectrum disorders[J]. Front Neurol, 2017, 8: 493. doi:10.3389/fneur.2017.00493.
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