유리체강내 항혈관내피세포성장인자주입술이 불필요한 말기 삼출황반변성의 해부학적 특징
Anatomical Characteristics of End-stage Exudative Age-related Macular Degeneration Refractory to Intravitreal Anti-vascular Endothelial Growth Factor Injection
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목적: 삼출성 나이관련황반변성으로 인해 법적 실명(20/1,000 이하)에 도달한 환자들의 빛간섭단층촬영에서 나타나는 소견을 조사하여 유리체강내 항혈관내피세포성장인자 치료가 불필요한 말기에 관찰되는 해부학적 특징을 알아보고자 하였다. 대상과 방법: 삼출성 나이관련황반변성을 진단받은 환자 중 유리체강내 항혈관내피세포성장인자주입술을 시행하여 최종내원일에 2줄 이상의 시력 호전을 보이거나 빛간섭단층촬영상 호전된 결과를 보인 환자 103명 120안(활동형 군)과 치료 받았음에도 반응이 없거나 첫 진단 시부터 반흔이 존재하여 최종 시력이 법적 실명에 도달한 환자 54명, 55안(말기형 군)의 의무 기록을 후향적으로 분석하였다. 연구 기간 중 최종내원일의 스펙트럼영역 빛간섭단층촬영을 통하여 활동형 군과 말기형 군의 망막 구조 변화를 비교분석하였다. 결과: 활동형 군에 비해 말기형 군의 평균 연령이 약 5세 정도 높게 나타났고, 경과관찰 중 망막내 출혈 및 망막하 출혈과 망막상피세포 파열의 발생 빈도가 말기형 군에서 유의하게 높았다(p<0.05). 빛간섭단층촬영에서 관찰되는 망막하액이나 망막내낭포액은 활동형 군에서 높은 빈도로 나타났고, 말기형 군 모두에서 망막하 고반사물질의 축적, 섬유혈관성 망막색소상피박리, 범위가 큰 광수용체내외절경계선의 파열이 관찰되었다. 활동형 군에 비해 말기형 군에서 망막색소상피박리의 크기와 두께, 황반중점두께, 황반중심두께, 망막하 고반사물질 두께가 유의하게 더 컸고(p<0.05), 말기형 군 대부분에서 최종적으로 원반반흔을 형성하였다. 결론: 말기 삼출성 나이관련황반변성 환자에서 경과관찰 중 망막 출혈이나 망막상피세포 파열이 발생하거나 원반반흔, 두꺼운 망막하고반사물질, 섬유혈관성 망막색소상피박리 및 범위가 큰 황반 부위의 광수용체내외절경계선 소실이 관찰된다면 유리체강내 항혈관내피성장인자의 낮은 치료 효과를 예상할 수 있고, 이는 향후 치료 종결 시점을 결정하는 데 참고가 될 것으로 보인다.
Abstract
Purpose: To analyze the anatomical characteristics on spectral-domain optical coherence tomography (SD-OCT) of patients who are legally blind (less than 20/1,000) due to end-stage exudative age-related macular degeneration (AMD) that does not require intravitreal anti-vascular endothelial growth factor (anti-VEGF) injection. Methods: After anti-VEGF injections (active group), 120 eyes of 103 exudative AMD patients experienced visual acuity improved by at least 2 lines or improvement on SD-OCT. In addition, 55 eyes of 54 end-stage exudative AMD patients who did not respond to treatment or who were legally blind due to foveal scar at the first visit (end-stage group) were evaluated retrospectively. Changes in retinal structures of the 2 groups were analyzed by SD-OCT at the last visit. Results: The mean age of the end-stage group was about 5 years older than the active group. During the follow-up period, subretinal hemorrhage, intraretinal hemorrhage and retinal pigment epithelium tear occurred more frequently in the end-stage group than in the active group (p < 0.05). Intra-retinal fluids and subretinal fluids were more frequently administered in the active group than in the end-stage group, and thick subretinal hyper-reflective materials (SRHRM), fibrovascular pigment epithelial detachment (PED) and extensive inner segment/outer segment (IS/OS) line disruption were observed in all eyes of the end-stage group. The size and thickness of PED, foveal thickness and SRHRM thickness were significantly larger in the end-stage group than in the active group (p < 0.05). Disciform retinal scars were eventually formed in most of the end-stage group. Conclusions: In end-stage exudative AMD, the presence of retinal hemorrhage and retinal pigment epithelium tear during follow- up, or the findings of thick SRHRM, fibrovascular PED, and extensive IS/OS line disruption on SD-OCT suggest weak expected effect of intravitreal anti-VEGF injection, which can act as a reference for determining the timing of treatment termination.
참고문헌 (29)
- Wong TY, "The natural history and prognosis of neovascular age-related macular degeneration: a systemic review of the literature and meta-analysis", Ophthalmology, 115, pp.116~126 (2008)
- Sunness JS, "Enlargement of atrophy and visual acuity loss in the geographic atrophy form of age-related macular degeneration", Ophthalmology, 106, pp.1768~1779 (1999)
- Pauleikhoff D, "Neovascular age-related macular degeneration: natural history and treatment outcomes", Retina, 25, pp.1065~1084 (2005)
- Bressler SB, "Introduction: understanding the role of angiogenesis and anti-angiogenic agents in age-related macular degeneration", Ophthalmology, 116(10 Suppl), pp.S1~S7 (2009)
- Witmer AN, "Vascular endothelial growth factors and angiogenesis in eye disease", Prog Retin Eye Res, 22, pp.1~29 (2003)
- Green WR, "Age-related macular degeneration histopathologic studies. The 1992 Lorenz E. Zimmerman Lecture", Ophthalmology, 100, pp.1519~1535 (1993)
- Wilgus TA, "Regulation of scar formation by vascular endothelial growth factor", Lab Invest, 8, pp.579~590 (2000)
- Michels S, "Systemic bevacizumab (Avastin) therapy for neovascular age-related macular degeneration twelve-week results of an uncontrolled open-label clinical study", Ophthalmology, 112, pp.1035~1047 (2005)
- Rosenfeld PJ, "Ranibizumab for neovascular age-related macular degeneration", N Engl J Med, 355, pp.1419~1431 (2006)
- Brown DM, "Ranibizumab versus verteporfin for neovascular age-related macular degeneration", N Engl J Med, 355, pp.1432~1444 (2006)
- Rosenfeld PJ, "Ranibizumab for neovascular age-related macular degeneration", N Engl J Med, 355, pp.1419~1431 (2006)
- Fung AE, "An optical coherence tomography-guided, variable dosing regimen with intravitreal ranibizumab (Lucentis) for neovascular age-related macular degeneration", Am J Ophthalmol, 143, pp.566~583 (2007)
- Gupta OP, "A treat and extend regimen using ranibizumab for neovascular age-related macular degeneration clinical and economic impact", Ophthalmology, 117, pp.2134~2140 (2010)
- Cohen SY, "Causes of unsuccessful ranibizumab treatment in exudative age-related macular degeneration in clinical settings", Retina, 32, pp.1480~1485 (2012)
- Daniel E, "Risk of scar in the comparison of age-related macular degeneration treatments trials", Ophthalmology, 121, pp.656~666 (2014)
- Rahimy E, "Multilayered pigment epithelial detachment in neovascular age-related macular degeneration", Retina, 34, pp.1289~1295 (2014)
- 조성우, "삼출성 연령관련황반변성에서 유리체강내 베바시주맙 주입술의 해부학적 비반응군 조사", 대한안과학회지, 51(11), pp.1464~1470 (2010), 대한안과학회
- 신주영, "Anti-VEGF-refractory Exudative Age-related Macular Degeneration: Differential Response According to Features on Optical Coherence Tomography", Korean Journal of Ophthalmology, 27(6), pp.425~432 (2013), 대한안과학회
- Varshney N, "Anti-VEGF response in macular hemorrhage and incidence of retinal pigment epithelial tears", Can J Ophthamol, 48, pp.210~215 (2013)
- Empeslidis T, "Incidence of retinal pigment epithelial tears and associated risk factors after treatment of age-related macular degeneration with intravitreal Anti-VEGF Injections", Open Ophthalmol J, 8, pp.101~104 (2014)
- Gutfleisch M, "Long-term visual outcome of pigment epithelial tears in association with anti-VEGF therapy of pigment epithelial detachment in AMD", Eye (Lond), 25, pp.1181~1186 (2011)
- Durkin SR, "Change in vision after retinal pigment epithelium tear following the use of anti-VEGF therapy for age-related macular degeneration", Graefes Arch Clin Exp Ophthalmol, 254, pp.1~6 (2016)
- Jaffe GJ, "Comparison of Age-related Macular Degeneration Treatments Trials Research Group. Macular morphology and visual acuity in the comparison of age-related macular degeneration treatments trials", Ophthalmology, 120, pp.1860~1870 (2013)
- Golbaz I, "Quantification of the therapeutic response of intraretinal, subretinal, and subpigment epithelial compartments in exudative AMD during anti-VEGF therapy", Invest Ophthalmol Vis Sci, 52, pp.1599~1605 (2011)
- Simader C, "Morphologic parameters relevant for visual outcome during anti-angiogenic therapy of neovascular age-related macular degeneration", Ophthalmology, 121, pp.1237~1245 (2014)
- Ores R, "Gray hyper-reflective subretinal exudative lesions in exudative age-related macular degeneration", Am J Ophthalmol, 158, pp.354~361 (2014)
- Shah VP, "Subretinal hyperreflective exudation associated with neovascular age-related macular degeneration", Retina, 34, pp.1281~1288 (2014)
- Tan ACS, "A perspective on the nature and frequency of pigment epithelial detachments", Am J Ophthalmol, 172, pp.13~27 (2016)
- Kim SY, "Morphometric analysis of the macula in eyes with disciform age-related macular degeneration", Retina, 22, pp.471~477 (2002)
