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1.
Case Rep Ophthalmol ; 8(1): 208-213, 2017.
Article in English | MEDLINE | ID: mdl-28512423

ABSTRACT

PURPOSE: To report a surgical technique for retinal detachment associated with optic disc pit (ODP) by using an internal limiting membrane (ILM) inverted flap as an obstacle between the vitreous cavity and subretinal space. CASE PRESENTATION: A 43-year-old man presented with decreased visual acuity in the right eye for 1 week due to macular detachment associated with ODP. After 2 unsuccessful surgeries, the retina was reattached by vitrectomy with an ILM inverted flap onto the ODP. CONCLUSION: Covering the pit with an inverted ILM flap is a reliable method for intercepting fluid from the vitreous cavity. Immediate absorption of subretinal fluid may lead to early macular attachment. This technique would be effective in managing ODP.

2.
Ophthalmologica ; 232(3): 170-8, 2014.
Article in English | MEDLINE | ID: mdl-25323920

ABSTRACT

PURPOSE: To investigate the incidence of and risk factors for a dissociated optic nerve fiber layer (DONFL) appearance after pars plana vitrectomy (PPV). METHODS: We retrospectively reviewed 189 eyes that underwent PPV with internal limiting membrane removal and judged the presence/absence of an apparent DONFL based on en face layer images produced by spectral-domain optical coherence tomography (SD-OCT). RESULTS: An apparent DONFL was observed in 47 (24.9%) eyes. The incidence of an apparent DONFL was significantly higher in the macular hole (MH) group (76.5%) than in the non-MH group (epiretinal membrane, diabetic macular edema, retinal vein occlusion, and others; 4.9%; p < 0.001). In the logistic regression analysis, surgical indication for MH was identified as the most significant DONFL risk factor (odds ratio 63.7; p = 1.05 × 10(-8)). CONCLUSION: Postoperative OCT en face layer imaging clarified that MH eyes are liable to have an apparent DONFL following PPV.


Subject(s)
Nerve Fibers/pathology , Optic Disk/pathology , Retinal Perforations/diagnosis , Tomography, Optical Coherence/methods , Aged , Epiretinal Membrane/surgery , Female , Humans , Male , Middle Aged , Postoperative Period , Retrospective Studies , Risk Factors , Visual Acuity/physiology , Vitrectomy
3.
Ophthalmologica ; 232(2): 92-6, 2014.
Article in English | MEDLINE | ID: mdl-24993059

ABSTRACT

BACKGROUND: To compare the outcomes of photodynamic therapy (PDT) between two different angiographic subtypes of polypoidal choroidal vasculopathy (PCV). METHODS: Ninety-three consecutive cases of PCV were classified into two phenotypes (42 type 1 and 51 type 2) according to the presence or absence of feeding vessels found on indocyanine green angiography. Full-dose PDT and retreatments were performed every 3 months as needed based on the findings on angiography. The best-corrected visual acuity (BCVA) was compared as the main outcome between type 1 and type 2 PCV up to 12 months after the initial PDT. RESULTS: The baseline greatest linear dimension (GLD) was significantly larger in type 1 PCV than type 2 PCV. The mean BCVA was significantly improved from baseline in type 2 PCV, while no improvement was found in type 1 PCV. Analysis with matching the GLD between both PCV subtypes did not change the original results. CONCLUSIONS: There may be a significantly different response to PDT between two angiographic phenotypes of PCV.


Subject(s)
Choroidal Neovascularization/drug therapy , Photochemotherapy , Polyps/drug therapy , Aged , Choroidal Neovascularization/classification , Choroidal Neovascularization/diagnosis , Coloring Agents , Female , Fluorescein Angiography , Humans , Indocyanine Green , Male , Polyps/classification , Polyps/diagnosis , Retrospective Studies , Treatment Outcome , Visual Acuity/physiology
4.
Pharmacogenomics ; 15(6): 833-43, 2014 Apr.
Article in English | MEDLINE | ID: mdl-24897289

ABSTRACT

AIM: This study was conducted to evaluate the possible clinical and genetic indicators for an early response to intravitreal ranibizumab (IVR) in exudative age-related macular degeneration (AMD). PATIENTS & METHODS: The records of 120 eyes from 120 Japanese patients with treatment-naive exudative AMD were retrospectively reviewed. Three consecutive IVR treatments were performed every month. Achievement of anatomical resolution was evaluated by ophthalmoscopy and optical coherence tomography. Multivariable logistic regression analysis was conducted by analyzing SNPs in the ARMS2 locus (A69S) and in the CFH gene (I62V and Y402H), in addition to clinical factors. RESULTS: The mean central retinal thickness of overall patients was significantly decreased (-120.1 ± 122.8 µm, p = 2.7 × 10(-19)) at 3 months after the initial treatment. In the logistic regression analysis, the poor anatomical resolution of the lesion at 3 months was associated with the combination of CFH I62V + CFH Y402H variants (p = 0.0021), and the polypoidal choroidal vasculopathy lesions (p = 0.044). CONCLUSION: The CFH variants and the polypoidal choroidal vasculopathy lesion may influence the early anatomical resolution with IVR in exudative AMD.


Subject(s)
Antibodies, Monoclonal, Humanized/therapeutic use , Macular Degeneration/drug therapy , Aged , Asian People/genetics , Complement Factor H/genetics , Female , Humans , Intravitreal Injections/methods , Macular Degeneration/genetics , Male , Polymorphism, Single Nucleotide/genetics , Proteins/genetics , Ranibizumab , Retina/drug effects , Retrospective Studies
5.
Pediatr Int ; 55(3): 366-8, 2013 Jun.
Article in English | MEDLINE | ID: mdl-23782366

ABSTRACT

We report a monochorionic diamniotic twin pair born at 29 weeks of gestation in which both twins developed severe retinopathy of prematurity (ROP) with retinal detachment. The pregnancy was terminated due to reversal of donor-recipient phenotypes in possible TTTS. Both twins had unstable cardiopulmonary status during the first week, and developed chronic lung disease. The larger twin, born at 1372 g, developed stage 4a ROP in both eyes, and the smaller twin, born at 1168 g, developed stage 4a ROP in the left eye. Genetic analysis of NDP, FZD4, LRP5, TSPAN12 genes revealed no mutations; however, VEGF gene polymorphism analysis showed heterozygous carrier state of the VEGF 936T allele in both twins, which is a risk factor for threshold ROP in Japanese newborn infants. We speculate the synergistic effects of unstable perinatal cardiopulmonary status and genetic predisposition due to VEGF 936C>T polymorphism caused the development of severe ROP with retinal detachment.


Subject(s)
Diseases in Twins/diagnosis , Diseases in Twins/genetics , Retinal Detachment/diagnosis , Retinal Detachment/genetics , Retinopathy of Prematurity/diagnosis , Retinopathy of Prematurity/genetics , Twins, Monozygotic/genetics , Adult , Alleles , Cesarean Section , Diseases in Twins/therapy , Female , Fetofetal Transfusion/diagnosis , Fetofetal Transfusion/genetics , Follow-Up Studies , Genetic Carrier Screening , Genetic Predisposition to Disease/genetics , Gestational Age , Heart Arrest/diagnosis , Heart Arrest/genetics , Heart Arrest/therapy , Humans , Intensive Care Units, Neonatal , Pregnancy , Respiratory Distress Syndrome, Newborn/diagnosis , Respiratory Distress Syndrome, Newborn/genetics , Respiratory Distress Syndrome, Newborn/therapy , Retinal Detachment/therapy , Retinopathy of Prematurity/therapy , Risk Factors , Vascular Endothelial Growth Factor A/genetics
6.
BMC Ophthalmol ; 13: 10, 2013 Apr 04.
Article in English | MEDLINE | ID: mdl-23557322

ABSTRACT

BACKGROUND: The effects of intravitreal ranibizumab (IVR) against exudative age-related macular degeneration (AMD) may be different associated with the lesion phenotype. This study was conducted to compare the outcomes of IVR between two different phenotypes of exudative AMD: typical neovascular AMD (tAMD) and polypoidal choroidal vasculopathy (PCV). METHODS: This is a retrospective cohort study of 54 eyes from 54 subfoveal exudative AMD patients (tAMD 24, PCV 30 eyes). Three consecutive IVR treatments (0.5 mg) were performed every month, followed by re-injections as needed. Change in the best-corrected visual acuity (BCVA) and central retinal thickness (CRT) were then compared between the tAMD and PCV groups over 12 months of follow-up. RESULTS: The mean BCVA was significantly improved (-0.11 logMAR units) at month 3 after the initial IVR (p <0 .001, Wilcoxon signed-rank test), and was sustained up to 12 months in all AMD patients (p =0.02). In the subgroup analysis, the tAMD group showed a significant improvement in their mean BCVA (-0.06, -0.17, -0.15 and -0.16 logMAR units at 1, 3, 6 and 12 months, respectively), but there was only a slight but non-significant improvement in the PCV group. The improvement in the BCVA was significantly greater in the tAMD group than in the PCV group (p = 0.043, repeated measures ANOVA) over 12 months. Both phenotypes showed significant improvements in the CRT during 12 months after the initial IVR. CONCLUSIONS: IVR is an effective therapy for tAMD and PCV in the BCVA improvement in Japanese patients over 12 months of follow-up. The phenotype of tAMD showed a significantly better outcome with IVR than PCV in terms of BCVA improvement.


Subject(s)
Angiogenesis Inhibitors/administration & dosage , Antibodies, Monoclonal, Humanized/administration & dosage , Choroid Diseases/drug therapy , Macular Degeneration/drug therapy , Polyps/drug therapy , Aged , Choroid Diseases/pathology , Choroid Diseases/physiopathology , Female , Follow-Up Studies , Humans , Intravitreal Injections , Logistic Models , Macular Degeneration/pathology , Macular Degeneration/physiopathology , Male , Middle Aged , Ranibizumab , Retrospective Studies , Visual Acuity
7.
Br J Ophthalmol ; 97(6): 770-4, 2013 Jun.
Article in English | MEDLINE | ID: mdl-23603482

ABSTRACT

BACKGROUND: Choroidal neovascularisation is often associated with pathological myopia. Bisphosphonates (BP), the preferred drug for treatment of osteoporosis, are known to have anti-angiogenic effects. OBJECTIVE: To compare the therapeutic effects of oral BP with anti-vascular endothelial growth factor therapy (anti-VEGF) and photodynamic therapy (PDT) for myopic choroidal neovascularisation (mCNV) over 2 years of follow-up. METHODS: One hundred eyes of 96 consecutive patients with mCNV who underwent oral BP treatment (alendronate 5 mg/day or 35 mg/week), anti-VEGF therapy, PDT or observation only were followed up for 2 years. The best-corrected visual acuity (BCVA) and the central retinal thickness (CRT) in optical coherence tomography were compared among the treatment groups. RESULTS: The mean BCVA of the patients was maintained for up to 2 years in the BP and PDT groups. In the anti-VEGF group, the mean BCVA was significantly improved but was significantly worse in the no-treatment group. The visual outcomes were significantly better in the BP, PDT and anti-VEGF groups than the no-treatment group over 2 years of follow-up (-0.28, -0.26 and -0.39 logMAR units, p=0.032, 0.021 and 0.0004, respectively). The mean CRT was significantly decreased in all treatment groups (-84, -121 and -122 mm, p=0.0025, 0.017 and 0.000025, respectively). CONCLUSIONS: Oral BP should be investigated further as possible therapeutic and preventive drugs for mCNV.


Subject(s)
Angiogenesis Inhibitors/administration & dosage , Choroidal Neovascularization/drug therapy , Diphosphonates/administration & dosage , Myopia, Degenerative/drug therapy , Photochemotherapy/methods , Vascular Endothelial Growth Factor A/antagonists & inhibitors , Administration, Oral , Aged , Choroidal Neovascularization/pathology , Female , Follow-Up Studies , Humans , Male , Middle Aged , Myopia, Degenerative/pathology , Pilot Projects , Tomography, Optical Coherence , Treatment Outcome , Visual Acuity/drug effects
8.
Jpn J Ophthalmol ; 57(3): 308-15, 2013 May.
Article in English | MEDLINE | ID: mdl-23443899

ABSTRACT

PURPOSE: To investigate the effects of reproducibility of optical coherence tomography (OCT) measurements and imaging alignment on predictive performance for visual outcome following macular hole (MH) surgery. METHODS: We retrospectively reviewed 50 eyes that underwent MH surgery. Preoperative cross-sectional images through the center of the MH (on-center image) and through an off-center point (off-center image) were obtained from the OCT data. In each image, the following OCT parameters were either measured or calculated: minimum diameter, base diameter, hole height, temporal and nasal arm length, photoreceptor inner segment/outer segment (IS/OS) defect length, the hole form factor, the macular hole index and the tractional hole index. The IS/OS defect area was also measured. RESULTS: The reproducibility of OCT parameter values was moderate to high, and there was a significant difference in the mean measurement values between the on- and off-center images. Predictive values varied between sessions and raters, and only the preoperative photoreceptor IS/OS defect length consistently showed significant correlation with postoperative visual outcome. CONCLUSIONS: Both the reproducibility and imaging alignment might affect the predictive performance of the OCT parameter for postoperative visual outcome following MH surgery. The preoperative photoreceptor IS/OS defect length seems to be the most useful parameter in this regard.


Subject(s)
Macula Lutea/pathology , Retinal Perforations/surgery , Tomography, Optical Coherence/methods , Visual Acuity , Vitrectomy/methods , Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Postoperative Period , Reproducibility of Results , Retinal Perforations/pathology , Retrospective Studies , Treatment Outcome
9.
Mol Vis ; 18: 2796-804, 2012.
Article in English | MEDLINE | ID: mdl-23213279

ABSTRACT

PURPOSE: To clarify the association between cluster of differentiation 36 (CD36) gene polymorphisms and the response to photodynamic therapy (PDT) in polypoidal choroidal vasculopathy (PCV). METHODS: One hundred and thirty-seven patients with PCV were enrolled. The patients were treated with PDT and followed up for more than 6 months. Retreatments were performed every 3 months as needed based on findings from angiography. Patients who showed an improvement in their best-corrected visual acuity at 6 months post-PDT were classified as PDT responders, and the others were defined as non-responders. For the 73 responders and 64 non-responders, 19 single nucleotide polymorphisms (SNPs) across the CD36 region were genotyped using the TaqMan assay. We analyzed the association between these variants and the visual outcomes of PDT. RESULTS: The allelic frequencies of the SNPs rs3211851, rs3173798, and rs3211908 showed nominally significant differences between the PDT responders and non-responders. Genotype association analysis revealed a significant association of SNP rs3173798 with the visual outcome of PDT in a dominant model. The presence of the C allele in rs3173798 was significantly associated with a poor response to PDT after multivariate logistic regression analysis with clinical pre-PDT parameters. The mean best-corrected visual acuity in the group with the TT genotype of rs3173798 was significantly improved over 12 months of follow-up after the initial PDT. CONCLUSIONS: The coding variants in CD36 are possibly associated with the visual outcome of PDT in patients with PCV.


Subject(s)
CD36 Antigens/genetics , Choroid/metabolism , Choroidal Neovascularization/genetics , Photochemotherapy , Polymorphism, Single Nucleotide , Aged , Aged, 80 and over , Alleles , Angiogenesis Inhibitors/administration & dosage , Choroid/drug effects , Choroid/pathology , Choroid/radiation effects , Choroidal Neovascularization/drug therapy , Choroidal Neovascularization/pathology , Female , Fluorescein Angiography , Gene Frequency , Genotype , Humans , Light , Male , Photosensitizing Agents/administration & dosage , Tomography, Optical Coherence , Treatment Outcome , Visual Acuity/drug effects , Visual Acuity/radiation effects
10.
Mol Vis ; 18: 121-7, 2012.
Article in English | MEDLINE | ID: mdl-22275803

ABSTRACT

PURPOSE: To clarify the association of cluster of differentiation 36 (CD36) variants with polypoidal choroidal vasculopathy (PCV) and compare them with those in typical neovascular age-related macular degeneration (tAMD). METHODS: We included 349 Japanese AMD patients (210 PCV, 139 tAMD) and 198 age-matched controls. Four tag single-nucleotide polymorphisms (SNPs)-rs10499862, rs3173798, rs3211883, and rs3173800-in the CD36 region were genotyped using the TaqMan assay. Allelic and genotypic frequencies of the SNPs were tested. RESULTS: Although none of the SNPs tested were associated with PCV, the allelic frequencies of rs3173798 and rs3173800 were significantly different between PCV and tAMD patients. Genotype association analysis demonstrated different associations of these two SNPs between PCV and tAMD in the genotype model. Haplotype analysis revealed that the association of the major haplotype (T-T-T-T) at four selected SNPs in CD36 differed significantly between PCV and tAMD patients. CONCLUSIONS: The CD36 region may be associated with the difference in genetic susceptibility for PCV and tAMD.


Subject(s)
Choroidal Neovascularization/genetics , Genetic Association Studies , Genetic Predisposition to Disease , Macular Degeneration/genetics , Polymorphism, Single Nucleotide/genetics , Aged , Aged, 80 and over , CD36 Antigens/genetics , Case-Control Studies , Female , Haplotypes/genetics , Humans , Male , Middle Aged
11.
Eur J Ophthalmol ; 22(2): 210-5, 2012.
Article in English | MEDLINE | ID: mdl-21534251

ABSTRACT

PURPOSE: To compare the efficacy of anti-vascular endothelial growth factor (VEGF) therapy versus photodynamic therapy (PDT) for myopic choroidal neovascularization (mCNV). METHODS: This study is a retrospective interventional study. Forty-two eyes from 42 patients with mCNV (36 subfoveal, 4 juxtafoveal, and 2 extrafoveal) treated and followed up for more than 6 months were included. Twenty eyes from 20 patients were treated by PDT (PDT group) at 1.5 ± 0.9 months after the symptoms and 22 eyes from 22 patients were treated by anti-VEGF therapy (anti-VEGF group) at 0.9 ± 0.8 months after the symptoms. Photodynamic therapy was performed, followed up, and retreated by standard procedures. Anti-VEGF therapy was repeated as needed. Gender, age, best-corrected visual acuity (BCVA), greatest linear dimension (GLD), central retinal thickness (CRT), and outer nuclear layer (ONL) thickness at the fovea were then compared between the anti-VEGF and PDT groups. RESULTS: No differences were detected in baseline parameters between the anti-VEGF and PDT groups. The mean BCVA (logMAR) at month 3 and 6 after the initial treatment was improved (-0.30 and -0.29) from baseline in the anti-VEGF group, which was statistically significant (p=0.0048 and 0.021, respectively). In the PDT group, modest improvements were observed in the mean BCVA at the same time periods (-0.05 and -0.10) with no statistical significance (p=0.79 and 0.90, respectively). The mean CRT was significantly reduced from baseline to month 6 in the anti-VEGF and PDT groups. The ONL thickness was significantly reduced in both groups, although the magnitude was significantly greater in the PDT group than the anti-VEGF group. CONCLUSIONS: Treatment with anti-VEGF therapy had significantly better visual outcomes than PDT for mCNV.


Subject(s)
Angiogenesis Inhibitors/therapeutic use , Choroidal Neovascularization/drug therapy , Myopia, Degenerative/complications , Photochemotherapy , Vascular Endothelial Growth Factor A/antagonists & inhibitors , Aged , Antibodies, Monoclonal, Humanized/therapeutic use , Bevacizumab , Choroidal Neovascularization/etiology , Choroidal Neovascularization/physiopathology , Coloring Agents , Female , Fluorescein Angiography , Follow-Up Studies , Humans , Indocyanine Green , Intravitreal Injections , Male , Photosensitizing Agents/therapeutic use , Porphyrins/therapeutic use , Ranibizumab , Retrospective Studies , Tomography, Optical Coherence , Treatment Outcome , Verteporfin , Visual Acuity/physiology
12.
PLoS One ; 6(12): e28847, 2011.
Article in English | MEDLINE | ID: mdl-22174912

ABSTRACT

BACKGROUND: Genetic variants in the complement component 3 gene (C3) have been shown to be associated with age-related macular degeneration (AMD) in Caucasian populations of European descent. In particular, a nonsynonymous coding variant, rs2230199 (R102G), is presumed to be the most likely causal variant in the C3 locus based on strong statistical evidence for disease association and mechanistic functional evidence. However, the risk allele is absent or rare (<1%) in Japanese and Chinese populations, and the association of R102G with AMD has not been reported in Asian populations. Genetic heterogeneity of disease-associated variants among different ethnicities is common in complex diseases. Here, we sought to examine whether other common variants in C3 are associated with wet AMD, a common advanced-stage manifestation of AMD, in a Japanese population. METHODOLOGY/PRINCIPAL FINDINGS: We genotyped 13 tag single nucleotide polymorphisms (SNPs) that capture the majority of common variations in the C3 locus and tested for associations between these SNPs and wet AMD in a Japanese population comprising 420 case subjects and 197 controls. A noncoding variant in C3 (rs2241394) exhibited statistically significant evidence of association (allelic P = 8.32 × 10(-4); odds ratio = 0.48 [95% CI = 0.31-0.74] for the rs2241394 C allele). Multilocus logistic regression analysis confirmed that the effect of rs2241394 was independent of the previously described loci at ARMS2 and CFH, and that the model including variants in ARMS2 and CFH plus C3 rs2241394 provided a better fit than the model without rs2241394. We found no evidence of epistasis between variants in C3 and CFH, despite the fact that they are involved in the same biological pathway. CONCLUSIONS: Our study provides evidence that C3 is a common AMD-associated locus that transcends racial boundaries and provides an impetus for more detailed genetic characterization of the C3 locus in Asian populations.


Subject(s)
Asian People/genetics , Complement C3/genetics , Genetic Predisposition to Disease , Macular Degeneration/genetics , Macular Degeneration/prevention & control , Polymorphism, Single Nucleotide/genetics , Aged , Aged, 80 and over , Female , Genetic Association Studies , Genetic Loci/genetics , Genetic Markers , Haplotypes/genetics , Humans , Japan , Linkage Disequilibrium/genetics , Logistic Models , Male , Middle Aged
13.
Case Rep Ophthalmol ; 2(3): 314-8, 2011 Sep.
Article in English | MEDLINE | ID: mdl-22125532

ABSTRACT

PURPOSE: To report a case of proliferative diabetic retinopathy (PDR) showing transient macular edema (ME) and deteriorated retinal function after intravitreal bevacizumab injection (IVB). METHODS AND RESULTS: A 53-year-old man received IVB (1.25 mg/0.05 ml) in both eyes for the treatment of PDR. There was no treatment-related complication. However, he complained of photopsia in both eyes 6 h after the injection. Slit-lamp examination revealed mild cellular infiltrations (1+) in the anterior chamber in both eyes. Optical coherence tomography showed ME formation in the left eye. Both full-field and multifocal electroretinography (ERG) revealed the deterioration of all parameters in both eyes compared with pretreatment. The inflammation in the anterior segment and ME disappeared 1 day after the injection. ERG parameters were improved 9 days after the injection, except for the N1 and P1 amplitude of multifocal ERG in the left eye. CONCLUSION: We propose that patients who undergo IVB should be carefully informed and followed up for possible complications including temporal ME formation and retinal function deterioration.

14.
J Ophthalmol ; 2011: 742020, 2011.
Article in English | MEDLINE | ID: mdl-21772985

ABSTRACT

Purpose. To evaluate the early response to intravitreal ranibizumab (IVR) in two different phenotypes of age-related macular degenerations (AMD): typical neovascular AMD (tAMD) and polypoidal choroidal vasculopathy (PCV). Methods. Sixty eyes from 60 patients (tAMD 28, PCV 32 eyes) were recruited. Three consecutive IVR treatments (0.5 mg) were performed every month. Change in the best-corrected visual acuity (BCVA) and central retinal thickness (CRT) was then compared between the tAMD and PCV groups. Results. The mean BCVA logMAR was significantly improved at month 1 and month 3 after the initial IVR in the tAMD group, but there was no change in the PCV group. Both phenotypes showed significant improvements in the CRT during the 3 months after the initial IVR. There were no significant differences in the improvements of the CRT in the tAMD versus the PCV group. In the stepwise analysis, a worse pretreatment BCVA and tAMD lesions were significantly beneficial for a greater improvement of BCVA at 3 months after the initial IVR. Conclusions. The phenotype of tAMD showed a significantly better early response to IVR than PCV in terms of BCVA improvement.

15.
Ophthalmologica ; 226(2): 81-6, 2011.
Article in English | MEDLINE | ID: mdl-21625191

ABSTRACT

PURPOSE: To evaluate the retinal toxicity of intravitreal tissue plasminogen activator (tPA) injection for branch and central retinal vein occlusion (BRVO and CRVO) using the electroretinogram (ERG). PROCEDURES: Ten BRVO patients and 5 CRVO patients were enrolled. A complete examination including full-field ERG, visual acuity, central retinal thickness (CRT), and evaluation of systemic and ocular complications was performed before and after intravitreal tPA injection. RESULTS: No significant differences were found in the amplitude or implicit time of any ERG component after tPA injection, and no systemic or ocular complication was observed. The improvement of visual acuity was significant at month 3 in the BRVO group (p < 0.05) but not in the CRVO group. CRT significantly decreased over the course of 3 months in both groups (p < 0.01). CONCLUSION: Intravitreal tPA injection seems to be a safe and effective treatment option for macular oedema caused by retinal vein occlusions.


Subject(s)
Electroretinography/drug effects , Fibrinolytic Agents/administration & dosage , Macular Edema/drug therapy , Retinal Vein Occlusion/drug therapy , Tissue Plasminogen Activator/administration & dosage , Aged , Female , Fibrinolytic Agents/adverse effects , Humans , Intravitreal Injections , Macular Edema/etiology , Male , Prospective Studies , Retinal Vein Occlusion/complications , Tissue Plasminogen Activator/adverse effects , Treatment Outcome , Visual Acuity/physiology
16.
Mol Vis ; 17: 3574-82, 2011.
Article in English | MEDLINE | ID: mdl-22219653

ABSTRACT

PURPOSE: To investigate whether the A69S variant of the age-related maculopathy susceptibility 2 gene (ARMS2) has a different hereditary contribution in neovascular age-related macular degeneration (AMD) and polypoidal choroidal vasculopathy (PCV). METHODS: We initially conducted a comparative genetic analysis of neovascular AMD and PCV, genotyping the ARMS2 A69S variant in 181 subjects with neovascular AMD, 198 subjects with PCV, and 203 controls in a Japanese population. Genotyping was conducted using TaqMan technology. Results were then integrated into a meta-analysis of previous studies representing an assessment of the association between the ARMS2 A69S variant and neovascular AMD and/or PCV, comprising a total of 3,828 subjects of Asian descent. The Q-statistic test was used to assess between-study heterogeneity. Summary odds ratios (ORs) and 95% confidence intervals (CIs) were estimated using a fixed effects model. RESULTS: The genetic effect of the A69S variant was stronger in neovascular AMD (allelic summary OR=3.09 [95% CI, 2.71-3.51], fixed effects p<0.001) than in PCV (allelic summary OR=2.13 [95% CI, 1.91-2.38], fixed effects p<0.001). The pooled risk allele frequency was significantly higher in neovascular AMD (64.7%) than in PCV (55.6%). The population attributable risks for the variant allele were estimated to be 43.9% (95% CI, 39.0%-48.4%) and 29.7% (95% CI, 25.4%-34.0%) for neovascular AMD and PCV, respectively. No significant between-study heterogeneity was observed in any statistical analysis in this meta-analysis. CONCLUSIONS: Our meta-analysis provides substantial evidence that the ARMS2 A69S variant confers a significantly higher risk of neovascular AMD than PCV. Furthermore, there is compelling evidence that the risk attributable to the A69S variant differs between geographic atrophy and neovascular AMD. Together with defining the molecular basis of susceptibility, understanding the relationships between this genomic region and disease subtypes will yield important insights, elucidating the biologic architecture of this phenotypically heterogeneous disorder.


Subject(s)
Asian People/genetics , Choroid/metabolism , Choroidal Neovascularization/genetics , Macular Degeneration/genetics , Proteins/genetics , Retina/metabolism , Aged , Aged, 80 and over , Alleles , Amino Acid Substitution , Case-Control Studies , Choroid/pathology , Choroidal Neovascularization/metabolism , Female , Gene Frequency , Genetic Predisposition to Disease , Genotype , Humans , Macular Degeneration/metabolism , Male , Middle Aged , Molecular Typing , Odds Ratio , Polymorphism, Single Nucleotide , Retina/pathology , Risk Factors
17.
Case Rep Ophthalmol ; 1(2): 47-52, 2010 Sep 13.
Article in English | MEDLINE | ID: mdl-21060772

ABSTRACT

PURPOSE: Idiopathic macular holes (MHs) may occur bilaterally, and the spontaneous closure of MHs was documented previously. The median interval between the onset of MHs in each eye was reported to be 17.5 months. METHOD: We report a case of bilateral MHs which occurred and resolved spontaneously over a very short interval. RESULTS: A 48-year-old woman with no history of ocular disease complained of a central scotoma and metamorphopsia in the left eye. Stage 1A MH was diagnosed in the left eye on the initial visit, which resolved spontaneously with vitreofoveal separation after 1 month. After an additional month, she complained of a similar visual disturbance in the right eye. Stage 1B MH was found in the right eye, which showed spontaneous closure after 1 month in the same manner as the left eye. CONCLUSION: We present a unique case of bilateral MHs which occurred and resolved spontaneously within a very short time period. Careful observation of the non-involved eye is needed to address the risk of early onset bilateral MHs.

18.
Biochem Biophys Res Commun ; 400(4): 593-8, 2010 Oct 01.
Article in English | MEDLINE | ID: mdl-20804728

ABSTRACT

The multidrug resistance protein (MRP) MRP4/ABCC4 is an ATP-binding cassette transporter that actively effluxes endogenous and xenobiotic substrates out of cells. In the rodent retina, Mrp4 mRNA and protein are exclusively expressed in vascular endothelial cells, but the angiogenic properties of Mrp4 are poorly understood so far. This study aims to explore the angiogenic properties of MRP4 in human retinal microvascular endothelial cells (HRECs) utilizing the RNA interference (RNAi) technique. MRP4 expression was decreased at the mRNA and protein levels after stimulation with exogenous vascular endothelial growth factor in a dose-dependent manner. RNAi-mediated MRP4 knockdown in HRECs do not affect cell proliferation but enhances cell migration. Moreover, cell apoptosis induced by serum starvation was less prominent in MRP4 siRNA-treated HRECs as compared to control siRNA-treated HRECs. In a Matrigel-based tube-formation assay, although MRP4 knockdown did not lead to a significant change in the total tube length, MRP4 siRNA-treated HRECs assembled and aggregated into a massive tube-like structure, which was not observed in control siRNA-treated HRECs. These results suggest that MRP4 is uniquely involved in retinal angiogenesis.


Subject(s)
Apoptosis/genetics , Endothelium, Vascular/pathology , Multidrug Resistance-Associated Proteins/physiology , Neovascularization, Physiologic/genetics , Retina/physiology , Retinal Neovascularization/genetics , Retinal Vessels/pathology , Cell Movement/genetics , Cell Proliferation , Cells, Cultured , Endothelium, Vascular/metabolism , Gene Knockdown Techniques , Humans , Multidrug Resistance-Associated Proteins/genetics , Retina/cytology , Retinal Neovascularization/pathology , Retinal Vessels/metabolism
19.
J Ophthalmol ; 20102010.
Article in English | MEDLINE | ID: mdl-20706646

ABSTRACT

Purpose. Choroidal neovascularization (CNV) is often associated with age-related macular degeneration (AMD) and pathological myopia (PM). Bisphosphonates, the drug of choice to treat osteoporosis, have been recently reported to have anti-angiogenic effects. The purpose of this study is to investigate the therapeutic effects of oral bisphosphonates for CNV in humans. Methods. Thirty-six consecutive cases with CNV due to AMD or PM who declined anti-VEGF therapy were recruited. The patients were prescribed 5 mg of oral alendronates daily for 6 months. The best-corrected visual-acuity (BCVA), the lesion size in fundus photographs and fluorescein angiography, foveal thickness and total macular volume in optical coherence tomography were compared between pre- and post-treatment. Results. The mean BCVA of the patients was significantly improved after a months with the treatment in the AMD group. In the PM group, the mean BCVA was maintained up to 6 months with the treatment. The mean lesion size was significantly decreased by 3 months in both groups. The averages of foveal thickness and total macular volume were significantly reduced after 1 month of treatment in the AMD group.Conclusions. Oral bisphosphonate should be further investigated as a possible therapeutic and preventive drug for CNV due to AMD and PM.

20.
Brain Res ; 1283: 186-93, 2009 Aug 04.
Article in English | MEDLINE | ID: mdl-19505448

ABSTRACT

ATP-binding cassette (ABC) transporters at the blood-brain barrier (BBB) are responsible for the majority of the transcellular movement of various substrates, including various drugs, and contribute to the maintenance of brain homeostasis. Clinically, the abnormal expression of efflux transporters at the BBB is known to be associated with brain diseases such as epilepsy. In the retina, vascular endothelial cells outline the inner blood-retinal barrier (BRB) like the BBB, and some ABC efflux transporters are expressed in the adult retina. However, little is known about ABC transporter expression during retinal development or under pathological conditions. Here, we examined ABC transporter expression in the mouse retina, and demonstrated that P-glycoprotein (P-gp)/ABCB1, Mrp4/ABCC4, and Bcrp/ABCG2 were almost uniformly expressed in these blood vessels, including the capillaries and large vessels. This expression persisted throughout the developmental period, and the hyaloid vessels that normally feed the developing eye were immunoreactive for P-gp and Mrp4. Furthermore, we investigated ABC transporter expression in pathological angiogenesis using an oxygen-induced retinopathy model where hypoxia-induced preretinal neovascularization occurred around the central avascular retina. P-gp was prominently immunoexpressed but Mrp4 and Bcrp were weakly immunoexpressed, in the preretinal neovascular tufts. These findings will be helpful for understanding the roles of ABC transporters during both physiological and pathological retinal angiogenesis, and might provide new insights for safe and effective drug administration to infants or patients with angiogenic ocular disease.


Subject(s)
ATP-Binding Cassette Transporters/metabolism , Blood-Brain Barrier/metabolism , Oxygen/adverse effects , Retina/metabolism , Retinal Artery/metabolism , Retinopathy of Prematurity/metabolism , ATP Binding Cassette Transporter, Subfamily B, Member 1/metabolism , ATP Binding Cassette Transporter, Subfamily G, Member 2 , Animals , Blood-Brain Barrier/pathology , Blood-Brain Barrier/physiopathology , Disease Models, Animal , Endothelial Cells/cytology , Endothelial Cells/metabolism , Humans , Immunohistochemistry , Infant, Newborn , Male , Mice , Mice, Inbred C57BL , Mice, Inbred ICR , Microcirculation/physiology , Multidrug Resistance-Associated Proteins/metabolism , Neovascularization, Pathologic/metabolism , Neovascularization, Pathologic/pathology , Neovascularization, Pathologic/physiopathology , Retina/growth & development , Retina/physiopathology , Retinal Artery/growth & development , Retinal Artery/physiopathology , Retinopathy of Prematurity/pathology , Retinopathy of Prematurity/physiopathology
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