112
Views
9
CrossRef citations to date
0
Altmetric
Original Research

Altered Intrinsic Functional Connectivity of the Primary Visual Cortex in Patients with Neovascular Glaucoma: A Resting-State Functional Magnetic Resonance Imaging Study

, , ORCID Icon, ORCID Icon, ORCID Icon, ORCID Icon, , , & show all
Pages 25-33 | Published online: 07 Jan 2020

References

  • J W K, Jee D, La TY. Neovascular glaucoma after vitrectomy in patients with proliferative diabetic retinopathy. Medicine. 2017;96(10):e6263. doi:10.1097/MD.000000000000626328272234
  • Kwon J, Sung KR. Effect of preoperative intravitreal bevacizumab on the surgical outcome of neovascular glaucoma at different stages. J Ophthalmol. 2017;2017(3):1–7. doi:10.1155/2017/7672485
  • Al-Bahlal A, Khandekar R, Rubaie KA, et al. Changing epidemiology of neovascular glaucoma from 2002 to 2012 at king khaled eye specialist hospital, Saudi Arabia. Indian J Ophthalmol. 2017;65(10):969–973. doi:10.4103/ijo.IJO_33_1729044062
  • Rodrigues GB, Abe RY, Zangalli C, et al. Neovascular glaucoma: a review. Int J Retina Vitreous. 2016;2(1):26–35. doi:10.1186/s40942-016-0051-x27895936
  • Jia X, Duan X. Application of anti-VEGF agents in treatment of neovascular glaucoma and anti-scarring in filtering surgery. Chin j Ophthalmol. 2015;51(4):314–318.
  • Jaulim A, Ahmed B, Khanam T, et al. Branch retinal vein occlusion epidemiology, pathogenesis, risk factors, clinical features, diagnosis, and complications. an update of the literature. Retina. 2013;33(5):901–910. doi:10.1097/IAE.0b013e3182870c1523609064
  • Shenghong L, Ping L, Honghan G, et al. Intrinsic functional connectivity alterations of the primary visual cortex in primary angle-closure glaucoma patients before and after surgery: a resting-state fMRI study. PLoS One. 2017;12(1):e0170598. doi:10.1371/journal.pone.017059828122025
  • Kun D, Yong L, Xiaohe Y, et al. Altered functional connectivity of the primary visual cortex in subjects with amblyopia. Neural Plast. 2013;2013:1–8.
  • Zhu PW, Huang X, Ye L, et al. Altered intrinsic functional connectivity of the primary visual cortex in youth patients with comitant exotropia: a resting state fMRI study. Int J Ophthalmol. 2018;11(4):668–673. doi:10.18240/ijo.2018.04.2229675389
  • Yan X, Wang Y, Xu L, et al. Altered functional connectivity of the primary visual cortex in adult comitant strabismus: a resting-state functional MRI study. Curr Eye Res. 2019;44(3):316–323. doi:10.1080/02713683.2018.154064230375900
  • Chao-Gan Y, Yu-Feng Z, et al. DPARSF: a MATLAB toolbox for “Pipeline” data analysis of resting-state fMRI. Front Syst Neurosci. 2010;4:13–19. doi:10.3389/fnsys.2010.0001320577591
  • Ding K, Liu Y, Yan X, et al. Altered functional connectivity of the primary visual cortex in subjects with amblyopia. Neural Plast. 2013;2013:612086. doi:10.1155/2013/61208623844297
  • Burton H, Snyder AZ, Raichle ME. Resting state functional connectivity in early blind humans. Front Syst Neurosci. 2014;8(1):51–66. doi:10.3389/fnsys.2014.0005124778608
  • Wen Z, Zhou F-Q, Huang X, et al. Altered functional connectivity of primary visual cortex in late blindness. Neuropsychiatr Dis Treat. 2018;14:3317–3327. doi:10.2147/NDT.S18375130584305
  • Shao Y, Bao J, Huang X, et al. Comparative study of interhemispheric functional connectivity in left eye monocular blindness versus right eye monocular blindness: a resting-state functional MRI study. Oncotarget. 2018;9(18):14285–14295. doi:10.18632/oncotarget.v9i1829581843
  • Wang J, Li T, Zhou P, et al. Altered functional connectivity within and between the default model network and the visual network in primary open-angle glaucoma: a resting-state fMRI study. Brain Imaging Behav. 2016;11(4):1–10.
  • Ye L, Wei R, Huang X, et al. Reduction in interhemispheric functional connectivity in the dorsal visual pathway in unilateral acute open globe injury patients: a resting-state fMRI study. Int J Ophthalmol. 2018;11(6):1056–1060. doi:10.18240/ijo.2018.06.2629977823
  • Dan HD, Zhou FQ, Huang X, Xing YQ, Shen Y. Altered intra- and inter-regional functional connectivity of the visual cortex in individuals with peripheral vision loss due to retinitis pigmentosa. Vision Res. 2019;159:68–75. doi:10.1016/j.visres.2019.02.01330904614
  • Weibert K, Andrews TJ. Activity in the right fusiform face area predicts the behavioural advantage for the perception of familiar faces. Neuropsychologia. 2015;75:588–596. doi:10.1016/j.neuropsychologia.2015.07.01526187507
  • Scherf KS, Elbich D, Minshew N, et al. Individual differences in symptom severity and behavior predict neural activation during face processing in adolescents with autism. Neuroimage Clin. 2015;7:53–67. doi:10.1016/j.nicl.2014.11.00325610767
  • Dai H, Morelli JN, Ai F, et al. Resting-state functional MRI: functional connectivity analysis of the visual cortex in primary open-angle glaucoma patients. Hum Brain Mapp. 2013;34(10):2455–2463. doi:10.1002/hbm.v34.1022461380
  • Dong JW, Brennan NMP, Izzo G, et al. fMRI activation in the middle frontal gyrus as an indicator of hemispheric dominance for language in brain tumor patients: a comparison with broca’s area. Neuroradiology. 2016;58(5):513–520. doi:10.1007/s00234-016-1655-426847705
  • Marine V, Romain Q, Lorena C, et al. Frontal eye field, where art thou? Anatomy, function, and non-invasive manipulation of frontal regions involved in eye movements and associated cognitive operations. Front Integr Neurosci. 2014;8:66–90. doi:10.3389/fnint.2014.0006625202241
  • Fernandes HL, Stevenson IH, Phillips AN, et al. Saliency and saccade encoding in the frontal eye field during natural scene search. Cereb Cortex. 2014;24(12):3232–3245. doi:10.1093/cercor/bht17923863686
  • Japee S, Holiday K, Satyshur MD, Mukai I, Ungerleider LG. A role of right middle frontal gyrus in reorienting of attention: a case study. Front Syst Neurosci. 2015;9:23–49. doi:10.3389/fnsys.2015.0002325784862
  • Huang X, Li D, Li HJ, et al. Abnormal regional spontaneous neural activity in visual pathway in retinal detachment patients: a resting-state functional MRI study. Neuropsychiatr Dis Treat. 2017;13:2849–2854. doi:10.2147/NDT.S14764529200859
  • Szlyk JP, Little DM. An FMRI study of word-level recognition and processing in patients with age-related macular degeneration. Invest Ophthalmol Vis Sci. 2009;50(9):4487–4495. doi:10.1167/iovs.08-225819387076
  • Hamamatsu T, Nakagawa Y, Tamai M, et al. Visual processing in patients with macular hole. Tohoku J Exp Med. 2000;190(4):249–260. doi:10.1620/tjem.190.24910877507
  • Wirth M, Jann K, Dierks T, et al. Semantic memory involvement in the default mode network: a functional neuroimaging study using independent component analysis. Neuroimage. 2011;54(4):3057–3066. doi:10.1016/j.neuroimage.2010.10.03920965253
  • Freton M, Lemogne C, Bergouignan L, et al. The eye of the self: precuneus volume and visual perspective during autobiographical memory retrieval. Brain Struct Funct. 2014;219(3):959–968. doi:10.1007/s00429-013-0546-223553546
  • Bruner E, Preuss TM, Chen X, et al. Evidence for expansion of the precuneus in human evolution. Brain Struct Funct. 2016;222(2):1–8. doi:10.1007/s00429-016-1218-927033097
  • Zhu Y, Gao B, Hua J, et al. Effects of methylphenidate on resting-state brain activity in normal adults: an fMRI study. Neurosci Bull. 2013;29(1):16–27. doi:10.1007/s12264-013-1306-223361519
  • Annen J, Heine L, Ziegler E, et al. Function-structure connectivity in patients with severe brain injury as measured by MRI-DWI and FDG-PET. Hum Brain Mapp. 2016;37(11):3707–3720. doi:10.1002/hbm.v37.1127273334
  • Goffaux P, Lydia G-T, Marchand S, et al. Individual differences in pain sensitivity vary as a function of precuneus reactivity. Brain Topogr. 2014;27(3):366–374. doi:10.1007/s10548-013-0291-023636269
  • Vanni S, Tanskanen T, Seppa M, et al. Coinciding early activation of the human primary visual cortex and anteromedial cuneus. Proc Natl Acad Sci. 2001;98(5):2776–2780. doi:10.1073/pnas.04160089811226316
  • Huang R, Lu M, Song Z, Wang J. Long-term intensive training induced brain structural changes in world class gymnasts. Brain Struct Funct. 2015;220(2):625–644. doi:10.1007/s00429-013-0677-524297657
  • Lai CH, Wu YT. Decreased regional homogeneity in lingual gyrus, increased regional homogeneity in cuneus and correlations with panic symptom severity of first-episode, medication-na?ve and late-onset panic disorder patients. Psychiatry Res. 2013;211(2):127–131. doi:10.1016/j.pscychresns.2012.11.00623352831