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1.
Acta Diabetol ; 2024 Apr 02.
Artículo en Inglés | MEDLINE | ID: mdl-38565685

RESUMEN

AIMS: Previous structural, vascular density, and perfusion studies have mostly comprised type 1 and type 2 diabetes, even in the absence of retinopathy. The current study aimed to compare macular vessel density (VD) measurements between maturity-onset diabetes of the young (MODY) patients and controls. METHODS: The macular VD of superficial, deep retina, and choriocapillaris (CC), and central macular thickness (CMT), foveal avascular zone (FAZ), FAZ perimetry, VD of the total retina at 300 µm around the FAZ (FD), and acirculatory index (AI) measurements were taken and analyzed via OCT-A (RTVue XR 100-2 Avanti, AngioVue) and were compared between molecularly confirmed MODY (glucokinase (GCK) variants) patients and healthy controls. RESULTS: Twenty-five MODY patients and 30 healthy controls were included in the study. The mean plasma hemoglobin A1c level in the MODY group was 6.39 ± 0.38. The mean age was 13.8 ± 2.1 in the MODY group and was 12.6 ± 2.5 years among controls. There was no significant difference in terms of the age, superficial and deep retinal VD, FAZ, FAZ perimetry, CMT, FD, or AI between the groups. Compared to the healthy controls, a slight but significant increase in the CC-VD was detected in the MODY group, but only in the parafoveal and perifoveal regions (p = 0.034, p = 0.009). CONCLUSION: The significant CC-VD increase in the MODY group might be associated with hyperglycemia and/or relatively poor and vulnerable peripheral vascular CC perfusion compared to the central. Previous thickness and VD results of childhood or adolescent diabetes were distributed in a wider range, suggesting that various factors, including some not yet clearly defined, may affect the choroidal vasculature independently of glycemia or as a contributing factor.

2.
Medicine (Baltimore) ; 102(43): e35835, 2023 Oct 27.
Artículo en Inglés | MEDLINE | ID: mdl-37904394

RESUMEN

To evaluate the optical coherence tomography angiography (OCT-A) findings in patients with systemic lupus erythematosus (SLE). Twenty-eight eyes of 28 patients with SLE and 27 eyes of 27 age and sex matched healthy controls were enrolled in this cross-sectional study. The vessel densities in the macula and optic disc were evaluated using the OCT-A (Optovue, Inc., Freemont, CA). Foveal retinal thickness, retinal vascular density in superficial capillary plexus (SCP), deep capillary plexus, and choriocapillaris, foveal avascular zone (FAZ), acircularity index, foveal vessel density (FD), and non-flow area in the superficial retina, the capillary and all-vessels density in the peripapillary area and the inside-disc area were automatically measured using Angiovue software of OCT-A and compared between the groups. The foveal, parafoveal and perifoveal retinal vessel densities in the superficial and deep capillary plexus and choriocapillaris were similar between groups. FAZ area, FAZ perimetry, acirculatory index, FD and non-flow area did not show a statistically significant difference. The vessel density in the inside disc area was significantly lower in patients with SLE (46.3 ±â€…3.8%) compared to the control group (49.1 ±â€…4.8%) (P = .02). Our results demonstrate significant decrement in vessel density in the inside-disc area in patients with SLE. The lower vessel density measurement in the inside-disc area might be associated with early neurologic vascular impairment in SLE. Further studies are required to determine the clinical relevance of this finding.


Asunto(s)
Lupus Eritematoso Sistémico , Disco Óptico , Humanos , Disco Óptico/diagnóstico por imagen , Disco Óptico/irrigación sanguínea , Angiografía con Fluoresceína/métodos , Tomografía de Coherencia Óptica/métodos , Estudios Transversales , Vasos Retinianos/diagnóstico por imagen , Lupus Eritematoso Sistémico/complicaciones , Lupus Eritematoso Sistémico/diagnóstico por imagen
3.
Neuroophthalmology ; 46(6): 359-366, 2022.
Artículo en Inglés | MEDLINE | ID: mdl-36544578

RESUMEN

We aimed to assess the visual fields and optical coherence tomography (OCT) measurements in patients with multiple sclerosis (MS) to detect subclinical visual system disease. The study included 15 MS patients with previous optic neuritis (Group I), 17 MS patients without previous optic neuritis (Group II), and 14 healthy controls (Group III). Each subject underwent standard automated perimetry (SAP), frequency doubling technology perimetry (FDTP), and OCT. The mean deviation of SAP in Group I was lower than those in Groups II (p = .018) and III (p = .001). The pattern standard deviation of SAP in Group I was higher than those in Group III (p < .0001). The mean deviation of FDTP in Groups I and II was lower than those in Group III (p = .0001 and p = .016, respectively). The temporal quadrant of the retinal nerve fibre layer in Group I was thinner than those in Groups II and III (p = .005 and p = .003, respectively). The mean macular volume in Group I was thinner than those in Groups II and III (p = .004 and p = .002, respectively). A single method is inadequate for establishing early and/or mild visual impairment in MS. All conventional and non-conventional techniques are complementary in demonstrating subclinical visual damage in MS.

4.
Int Ophthalmol ; 42(8): 2625-2632, 2022 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-35355169

RESUMEN

PURPOSE: To investigate the effect of botulinum neurotoxin-A (BTX-A) treatment on dry eye symptoms, tear meniscus, corneal topography and corneal aberrometry in patients with benign essential blepharospasm (BEB) and hemifacial spasm (HFS). MATERIALS AND METHODS: This prospective study comprised of 6 patients with BEB and 20 patients with HFS. Tear meniscus height (TMH) and depth (TMD), tear break-up time (TBUT), corneal fluorescein staining score (CFSS), Schirmer I test, ocular surface disease index (OSDI) score, corneal topography [corneal power of flat axis (K1), corneal power of steep axis (K2), mean corneal power (Km), astigmatism and thinnest pachymetry] and anterior corneal aberrometry [spherical aberration (SA), vertical coma (vcoma), horizontal coma (hcoma), higher order root mean square (hRMS) and total RMS] were evaluated before BTX-A treatment, 3 weeks after BTX-A treatment and 2 months after BTX-A treatment. RESULTS: Six patients with BEB and 20 patients with HFS treated with BTX-A were evaluated in this study. Twenty contralateral spasm free eyes of 20 HFS patients were taken as control group. TMH and TMD were found to be significantly higher in eyes with spasm at both 3 weeks and 2 months after injection (TMH: 279.0 ± 123.2 at pretreatment, 380.5 ± 174.7 at third week and 317.0 ± 125.5 at second month p < 0.001 and p = 0.02, respectively), (TMD: 183.7 ± 59.7 at pretreatment, 235.7 ± 91.1 at third week and 209.8 ± 77.1 at second month p < 0.01 and p = 0.015, respectively). TBUT, CFSS, Schirmer I test values were similar (p > 0.05). OSDI scores decreased significantly from 29.6 ± 25.3 to 19.8 ± 20. p = 0.03 at third week and increased again by second month. K2 (43.9 ± 1.7 vs. 43.7 ± 1.6, p = 0.03) and astigmatism (0.8 ± 0.5 vs. 0.6 ± 0.4, p = 0.04) values were significantly lower at third week and increased again by second month. Pachymetry and aberrometric values did not change significantly. In the control group only Schirmer I test value decreased significantly at second month (10.5 ± 6.5 vs. 7.2 ± 5.6, p = 0.008), other parameters did not change. CONCLUSION: BTX-A injection increases tear meniscus and decrease symptoms related to dry eye disease in BEB and HFS patients. It decrease astigmatism and keratometry values, it does not cause a significant change in corneal aberrations. However the positive effects of BTX-A injection on ocular surface is temporary.


Asunto(s)
Astigmatismo , Blefaroespasmo , Toxinas Botulínicas Tipo A , Síndromes de Ojo Seco , Espasmo Hemifacial , Fármacos Neuromusculares , Astigmatismo/complicaciones , Blefaroespasmo/inducido químicamente , Blefaroespasmo/tratamiento farmacológico , Coma/inducido químicamente , Coma/complicaciones , Topografía de la Córnea , Síndromes de Ojo Seco/inducido químicamente , Síndromes de Ojo Seco/diagnóstico , Síndromes de Ojo Seco/tratamiento farmacológico , Fluoresceína , Espasmo Hemifacial/inducido químicamente , Espasmo Hemifacial/complicaciones , Espasmo Hemifacial/tratamiento farmacológico , Humanos , Estudios Prospectivos , Lágrimas
5.
Ther Adv Ophthalmol ; 13: 25158414211005305, 2021.
Artículo en Inglés | MEDLINE | ID: mdl-33948533

RESUMEN

BACKGROUND AND PURPOSE: Randomised-controlled clinical trials (the ANCHOR and MARINA) examined the intravitreal anti-vascular endothelial growth factor (anti-VEGF) efficacy for eyes having fluorescein angiographic classic and occult (OCC) neovascular lesions. No significant difference in the treatment response between the lesion types was observed. Fundus fluorescein angiography and optical coherence tomography (OCT) are complementary devices that provide information about neovascular age-related macular degeneration (n-AMD). The aim of this retrospective study was to compare the clinical aspects of fluorescein angiographic characteristics in predominantly classic (PDC) and OCC subtypes of n-AMD treated with intravitreal ranibizumab. METHODS: Treatment-naive fluorescein angiographic OCC-n-AMD and PDC-n-AMD patients, who received monthly intravitreal ranibizumab for 3 months after baseline, and were followed-up with pro re nata injections between March 2013 and February 2018, were included. Means of the visual acuity (VA), central macular thickness (CMT), and intravitreal injection and visit numbers of the groups were compared throughout 24 months. RESULTS: We included 41 eyes of PDC-n-AMD patients and 36 eyes of OCC-n-AMD patients. The mean ages were 74.5 ± 10.6 and 71.9 ± 9.4, respectively. The baseline, and 3-, 6-, 12-, 18-, and 24-month VA results of the OCC group were significantly better than those in the PDC. However, VA gain in the PDC group at 3, 6, and 12 months was significantly higher than that in the OCC group. The mean of baseline CMT of the PDC (353 ± 118 µm) was significantly higher than that in the OCC group (293 ± 64 µm). No significant differences in terms of the number of visits or injections, or CMT change from the baseline values between groups were observed. CONCLUSION: The OCC-n-AMD patients had better baseline and follow-up VA and CMT means than the PDC-n-AMD patients. However, the PDC-n-AMD patients are expected to benefit more than the OCC-n-AMD patients in terms of VA gains.

6.
J Pediatr Ophthalmol Strabismus ; 57(4): 251-256, 2020 Jul 01.
Artículo en Inglés | MEDLINE | ID: mdl-32687210

RESUMEN

PURPOSE: To describe the clinical characteristics and surgical outcomes of acquired comitant esotropia with symptomatic diplopia. METHODS: The clinical features and surgical outcomes of 27 patients with diplopia due to acquired comitant esotropia were retrospectively reviewed. Exclusion criteria were a history of prematurity, cerebral palsy, head trauma, or febrile illness before the onset of acquired comitant esotropia, incomitant strabismus, accommodative spasm, and divergence paralysis. Neurological evaluation and neuroimaging was normal in all patients. RESULTS: Mean age at onset of esotropia and diplopia was 17.8 ± 10.3 years (range: 6 to 44 years). Eighteen patients had simple myopia (range: -0.25 to -7.75 diopters [D]), 5 patients had hypermetropia (range: 0.50 to 1.50 D), and 4 patients had emmetropia. The angle of deviation prior to surgery was 35.6 ± 10.3 prism diopters (PD) for far and 38.0 ± 10.5 PD for near fixation. Twenty-three patients (85%) were prism responders. A history of excessive near work (≥ 4 hours a day) with digital displays was present in 21 (78%) patients. Diplopia resolved and some level of stereovision was achieved in all patients postoperatively. Three patients had recurrence of esotropia in long-term follow-up. CONCLUSIONS: The differentiation of a serious pathology from a straightforward optically or medically treatable condition in patients with a subacute or chronic history of diplopia is challenging for the clinician. The recognition of acquired comitant esotropia due to presumed intensive near activities with digital display may avoid time-consuming and costly laboratory investigations. Most of the patients in this series were prism responders and surgery for the prism-adapted angle was successful in restoring binocular vision. [J Pediatr Ophthalmol Strabismus. 2020;57(4):251-256.].


Asunto(s)
Diplopía/fisiopatología , Esotropía/diagnóstico , Esotropía/cirugía , Músculos Oculomotores/cirugía , Procedimientos Quirúrgicos Oftalmológicos , Adolescente , Adulto , Niño , Esotropía/fisiopatología , Movimientos Oculares/fisiología , Femenino , Humanos , Masculino , Estudios Retrospectivos , Resultado del Tratamiento , Visión Binocular/fisiología , Adulto Joven
7.
Ophthalmic Genet ; 41(3): 257-262, 2020 06.
Artículo en Inglés | MEDLINE | ID: mdl-32372681

RESUMEN

Familial Mediterranean fever (FMF) is a hereditary auto-inflammatory disease with accompanying findings of amyloidosis and vasculitis. M694V is one of the most common mutations associated with amyloidosis. This study compared the macular optical coherence tomography angiography measurements in FMF patients who were genetically verified to carry the M694V mutation of the MEFV gene to those in healthy controls. The vessel densities (VDs) of superficial (SVP) and deep vascular plexus (DVP) of the retina, and choriocapillaris, foveal avascular zone (FAZ) perimetry, foveal VD 300µ around the FAZ (FD-300), acirculatory index (AI) and non-flow area were measured with  optical coherence tomography angiography (OCT-A). The FMF and control groups were matched for age and gender. Compound heterozygous pathogenic variants were excluded. Thirty-eight FMF patients with M694V mutations (28 heterozygous and 10 homozygous) and 40 healthy controls were included. The two groups were similar with the regard to age and gender (P=0.88 and P=0.49, respectively). None of the investigated parameters, including the vessel densities of the SVP and DVP, and choriocapillaris, FAZ perimetry, FD-300, AI, and non-flow area showed a statistically significant difference between the FMF and control groups. The macular vessel density measurements and FAZ parameters of FMF patients with M694V mutations do not differ from age- and sex-matched healthy controls.


Asunto(s)
Fiebre Mediterránea Familiar/patología , Fóvea Central/patología , Mácula Lútea/patología , Mutación , Neovascularización Patológica , Pirina/genética , Tomografía de Coherencia Óptica/métodos , Adulto , Estudios de Casos y Controles , Fiebre Mediterránea Familiar/diagnóstico por imagen , Fiebre Mediterránea Familiar/genética , Femenino , Fóvea Central/diagnóstico por imagen , Fóvea Central/metabolismo , Marcadores Genéticos , Humanos , Mácula Lútea/diagnóstico por imagen , Mácula Lútea/metabolismo , Masculino
8.
J Ocul Pharmacol Ther ; 36(7): 540-544, 2020 09.
Artículo en Inglés | MEDLINE | ID: mdl-32250190

RESUMEN

Purpose: Olopatadine hydrochloride 0.1% is one of the known primary topical treatments in ocular allergy. Although olopatadine is a worldwide used medication, the changes in pupil diameter, cornea, and anterior chamber associated with its use have not been studied in detail. In this prospective study, we aimed to determine the amount of mydriasis and explore the possible corneal and anterior chamber alterations after 0.1% topical olopatadine. Methods: A total of 77 eyes from 77 ocular-allergy diagnosed patients between 18 and 40 years were investigated in this prospective study. Thirty-nine eyes of 39 patients received topical olopatadine, and 38 eyes of 38 patients received sterile distilled water, randomly. Pentacam (Oculus Optikgeräte GmbH, Wetzlar, Germany) topography was used to assess the pupil and anterior chamber measurements at baseline and after 45 min of olopatadine or sterile distilled water instillation. Results: The differences between the baseline and 45th-min measurements for corneal thickness, anterior chamber depth, angle, and volume did not reach a statistical significance in the olopatadine or control groups. The pupil diameter significantly increased from 3.19 ± 0.62 to 3.36 ± 0.62 mm in the olopatadine group (P < 0.001), and remained relatively unchanged in the control group (P = 0.06). Conclusion: Olopatadine 0.1% does not lead to a significant change in corneal topography or anterior chamber parameters. However, it causes a slight but statistically significant increase in pupil diameter.


Asunto(s)
Cámara Anterior/efectos de los fármacos , Antialérgicos/efectos adversos , Clorhidrato de Olopatadina/efectos adversos , Pupila/efectos de los fármacos , Administración Oftálmica , Adolescente , Adulto , Antialérgicos/administración & dosificación , Córnea/efectos de los fármacos , Córnea/metabolismo , Topografía de la Córnea , Femenino , Humanos , Masculino , Clorhidrato de Olopatadina/administración & dosificación , Estudios Prospectivos , Adulto Joven
9.
Turk J Ophthalmol ; 48(4): 166-170, 2018 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-30202611

RESUMEN

OBJECTIVES: To assess the long-term effects of soft contact lenses (SCL) on the cornea and anterior chamber by topography. MATERIALS AND METHODS: Thirty-nine eyes of 22 healthy patients were included in this prospective study. Changes in corneal and anterior chamber parameters before and after 12 months of daily SCL use (Air Optix Aqua, Air Optix Aqua for Astigmatism, Acuvue Oasys and Acuvue Oasys for Astigmatism) were evaluated with Pentacam (Oculus, Germany). RESULTS: Best corrected visual acuity with toric SCL was significantly better compared to spectacles in the toric SCL group (0.98±0.34 vs 0.94±0.72, p=0.004). None of the corneal (horizontal and vertical keratometry, corneal volume, anterior and posterior corneal astigmatism, corneal pachymetry of apex and thinnest location) and anterior chamber (anterior chamber depth, volume and angle) parameters showed a statistically significant change after long-term daily wear of SCLs. CONCLUSION: The results of this study revealed that long-term wear of current high oxygen permeable and relatively low modulus silicone hydrogel SCLs does not impact cornea and anterior chamber morphology or volumetric parameters. Furthermore, toric silicone hydrogel SCLs can provide better visual performance than spectacles.

10.
J Pediatr Ophthalmol Strabismus ; 55: e14-e15, 2018 Jul 26.
Artículo en Inglés | MEDLINE | ID: mdl-30074605

RESUMEN

Horner syndrome is a rare but likely underdiagnosed complication of tonsillary surgery. The authors report the case of a 2.5-year-old boy who developed miosis and mild ptosis after radiofrequency tonsil ablation surgery. Pharmacologic testing with apraclonidine 0.5% eye drops confirmed left Horner syndrome. This case highlights the close anatomical relationship between the tonsils and cervical sympathetic trunk and draws attention to the occurrence of Horner syndrome after tonsillectomy. [J Pediatr Ophthalmol Strabismus. 2018;55:e14-e15.].


Asunto(s)
Ablación por Catéter/efectos adversos , Síndrome de Horner/etiología , Enfermedad Iatrogénica , Tonsila Palatina/cirugía , Complicaciones Posoperatorias , Tonsilitis/cirugía , Preescolar , Humanos , Masculino
11.
J Pediatr Endocrinol Metab ; 31(8): 855-860, 2018 Aug 28.
Artículo en Inglés | MEDLINE | ID: mdl-29935116

RESUMEN

BACKGROUND: The purpose of this study was to evaluate the macular choroidal thickness in obese children with and without insulin resistance (IR). METHODS: Thirty-six patients with obesity and 26 healthy volunteers were included in this cross-sectional study. The choroidal thickness was measured with enhanced depth imaging optical coherence tomography (EDI-OCT) at the fovea and at positions 500 µm, 1000 µm, 1500 µm nasal and temporal to the fovea. The choroidal thickness measurements of the groups were compared and the correlation between the homeostasis model assessment of insulin resistance (HOMA-IR) and choroidal thickness values was evaluated. RESULTS: The average choroidal thickness in the obese group was significantly lower than that of controls at locations 1000 µm (303.31±58.52 vs. 340.58±69.47, p=0.026) and 1500 µm (284.14±65.06 vs. 336.85±71.37, p=0.004) temporal to the fovea. A subgroup analysis depending on the presence of IR revealed that the choroidal thickness measurements at all positions were thinner in obese children without IR compared to children with IR and healthy controls. This thinning reached a statistical significance at locations 500 µm temporal, 1000 µm temporal and 1500 µm temporal to the fovea (p=0.03, p=0.009 and p=0.006; respectively). There was a moderate correlation between the choroidal thickness measurements and HOMA-IR values (r-values between 0.37 and 0.48; p<0.05). CONCLUSIONS: Our results suggest that obesity and IR may have an influence on the choroidal thickness in children. Longitudinal studies will clarify whether these choroidal changes are progressive and are a sign of microvascular dysfunction in childhood obesity.


Asunto(s)
Coroides/diagnóstico por imagen , Coroides/patología , Diagnóstico por Imagen/métodos , Resistencia a la Insulina , Obesidad/fisiopatología , Tomografía de Coherencia Óptica/métodos , Estudios de Casos y Controles , Niño , Estudios Transversales , Femenino , Estudios de Seguimiento , Humanos , Masculino , Pronóstico
12.
Laterality ; 22(4): 412-418, 2017 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-27461553

RESUMEN

Physiological palpebral fissure asymmetry is a common observation in a physician's everyday practice. The goal of this study was to examine the relationship between palpebral fissure height (PFH) and ocular dominance. Sixty-nine healthy volunteers (42 female, 27 male) were included in this research, and ocular dominance was determined using hole-in-the-card and pointing-a-finger tests. Those volunteers with inconsistent test results were excluded. Standard photographs were taken of all of the subjects in the primary position with a consistent background and photographic equipment. The PFHs were measured using an ImageJ analyser, and a mixed ANOVA was used for the statistical analysis. Overall, 87% of the participants showed small differences in their PFHs, with their dominant eyes being significantly wider than their non-dominant eyes (10.51 ± 0.97 vs. 10.32 ± 1.03; p = .001). This study revealed that ocular dominance has a significant effect on the PFH. Further research is required to understand the importance of this association in daily practice.


Asunto(s)
Predominio Ocular/fisiología , Movimientos Oculares/fisiología , Párpados/anomalías , Párpados/fisiopatología , Adolescente , Adulto , Análisis de Varianza , Estudios Transversales , Femenino , Humanos , Masculino , Estudios Prospectivos , Grabación de Cinta de Video , Agudeza Visual/fisiología , Adulto Joven
13.
J Pediatr Ophthalmol Strabismus ; 53(4): 218-22, 2016 Jul 01.
Artículo en Inglés | MEDLINE | ID: mdl-27182748

RESUMEN

PURPOSE: To identify the ocular features of children diagnosed as having 22q11.2 deletion syndrome in a Turkish population, which is the most common microdeletion syndrome with a wide range of facial and ocular abnormalities. METHODS: Sixteen children aged between 4 months and 18 years with a microdeletion in chromosome 22q11.2 underwent a detailed ophthalmological examination including uncorrected and best corrected visual acuity testing, stereoscopic vision examination, biomicroscopic and indirect fundus examination, and ocular motility testing. RESULTS: All patients had at least one ocular abnormality. The major abnormalities were eyelid abnormalities (eye hooding, narrow palpebral fissure, telecanthus, hypertelorism, sparse and thin eyebrows and eyelashes, blepharitis, and distichiasis), posterior embryotoxon, and tortuous retinal vessels in at least half of the patients. Other ophthalmological disorders were refractive errors, iris remnants, and strabismus. CONCLUSIONS: The chromosome 22q11.2 deletion syndrome is associated with a wide range of ocular disorders, which necessitates a comprehensive eye examination for appropriate treatment and follow-up. Ocular findings sometimes can provide a clue to the diagnosis of 22q11.2 deletion. [J Pediatr Ophthalmol Strabismus. 2016;53(4):218-222].


Asunto(s)
Anomalías Múltiples/diagnóstico , Síndrome de DiGeorge/diagnóstico , Anomalías del Ojo/diagnóstico , Adolescente , Niño , Preescolar , Percepción de Profundidad/fisiología , Párpados/anomalías , Femenino , Humanos , Lactante , Masculino , Errores de Refracción/diagnóstico , Enfermedades de la Retina/diagnóstico , Vasos Retinianos/anomalías , Agudeza Visual/fisiología
14.
Jpn J Ophthalmol ; 58(2): 172-6, 2014 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-24488155

RESUMEN

PURPOSE: To compare the optical coherence tomography (OCT) findings of neurofibromatosis-1 (NF-1) patients with/without optic pathway glioma (OPG) with those of healthy controls. METHODS: Ten patients with NF-1, 17 patients with NF-1-associated OPGs, and 17 control subjects were included in the study. Retinal nerve fiber layer (RNFL) and macular thickness findings measured with Stratus OCT were compared between the groups. RESULTS: The average RNFL thickness was significantly lower in the OPG group (76.72 ± 22.16 µm) than in the controls (108.89 ± 9.92 µm) and NF-1 patients without OPGs (111.17 ± 12.13 µm) (p < 0.001). The macular volume was also found to be lower in NF-1 patients with OPG (6.41 ± 0.66 mm(3)) than in the healthy controls (7.19 ± 0.36 mm(3); p = 0.001) and NF-1 patients without OPGs (7.25 ± 0.26 mm(3); p = 0.005). Following this analysis the OPG group was further subdivided into two categories: OPG patients with normal visual acuity (VA) and OPG patients with decreased VA. The statistical analysis was repeated for these four subgroups, revealing that while the decrement in the average RNFL thickness was significant for both OPG groups that in the macular volume was only significant for OPG patients with decreased VA. CONCLUSION: The results of our study suggest that RNFL thinning can be a helpful marker for the detection of OPGs in NF-1 patients. Larger studies with longitudinal data are required to confirm the role of OCT in the diagnosis and follow-up of these patients.


Asunto(s)
Fibras Nerviosas/patología , Neurofibromatosis 1/diagnóstico , Glioma del Nervio Óptico/diagnóstico , Células Ganglionares de la Retina/patología , Adolescente , Niño , Femenino , Humanos , Imagen por Resonancia Magnética , Masculino , Estudios Prospectivos , Retina/patología , Tomografía de Coherencia Óptica , Trastornos de la Visión/diagnóstico , Agudeza Visual , Campos Visuales
15.
Ocul Immunol Inflamm ; 21(5): 351-9, 2013 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-23730902

RESUMEN

PURPOSE: To compare serum and tear inflammatory and anti-inflammatory cytokine levels of rosacea patients with the healthy controls and evaluate the correlation of tear cytokine levels with tear function parameters. METHODS: Tear and serum interleukin (IL)-1α, IL-6, IL-8, IL-10, monocyte chemotactic protein-1 (MCP-1), macrophage inflammatory protein-1α (MIP-1α), epidermal growth factor (EGF), and vascular endothelial growth factor (VEGF) levels were measured using multiplex bead (Luminex) technology in 12 rosacea patients without ocular involvement (group 1), 20 rosacea patients with ocular involvement (group 2), and 22 healthy subjects (group 3). The correlation of the cytokines with tear function parameters was analyzed using Spearman correlation test. RESULTS: Tear IL-10 and VEGF levels were significantly lower in group 1 (median: 35.78 pg/mL and 427.29, respectively) and group 2 (median: 26.25 pg/mL and 348.31, respectively) than in group 3 (median: 75.96 pg/mL and 480.12, respectively) (p < 0.05). Mean serum IL-8 level was significantly lower in group 2 (median = 0) compared to group 3 (median = 3.98) (p = 0.02). Tear breakup time was found to be positively correlated with IL-10 (r = 0.46, p = 0.013) and inversely correlated with MCP-1 (r = -0.52, p = 0.004). CONCLUSIONS: Tear and serum levels of cytokines and growth factors measured with Luminex technology showed a large variation in rosacea and healthy subjects. Decreased levels of tear IL-10, an anti-inflammatory cytokine, may lead to an inflammatory ocular surface environment, exacerbate ocular surface inflammation, and deteriorate tear function tests. A bigger sample size, including rosacea patients with corneal involvement, is needed to confirm the role of cytokines in the pathogenesis of rosacea-associated ocular inflammation.


Asunto(s)
Citocinas/metabolismo , Enfermedades de los Párpados/metabolismo , Rosácea/metabolismo , Lágrimas/metabolismo , Adolescente , Adulto , Anciano , Diagnóstico Diferencial , Ensayo de Inmunoadsorción Enzimática , Enfermedades de los Párpados/diagnóstico , Femenino , Humanos , Masculino , Persona de Mediana Edad , Estudios Prospectivos , Rosácea/sangre , Rosácea/diagnóstico , Adulto Joven
16.
J AAPOS ; 15(1): 69-70, 2011 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-21315630

RESUMEN

A clival epidural hematoma is a rare lesion that usually develops after a hyperflexion or hyperextension injury of the neck, often in a child. A 5-year-old girl presented after a motor vehicle accident with multiple cranial neuropathies, including bilateral abducens nerve pareses and right facial, glossopharyngeal, and hypoglossal cranial nerve palsies. Neuroimaging identified a clival epidural hematoma. The child was observed and the hematoma resolved. The abducens nerve palsies resolved during the ensuing 14 months.


Asunto(s)
Enfermedades del Nervio Abducens/etiología , Traumatismos Cerebrovasculares/complicaciones , Diplopía/etiología , Hematoma Epidural Craneal/etiología , Enfermedades del Nervio Abducens/diagnóstico , Enfermedades del Nervio Abducens/fisiopatología , Accidentes de Tránsito , Traumatismos Cerebrovasculares/fisiopatología , Preescolar , Fosa Craneal Posterior , Diplopía/diagnóstico , Diplopía/fisiopatología , Femenino , Hematoma Epidural Craneal/diagnóstico , Hematoma Epidural Craneal/fisiopatología , Humanos , Imagen por Resonancia Magnética , Tomografía Computarizada por Rayos X , Agudeza Visual/fisiología
17.
J AAPOS ; 14(4): 323-7, 2010 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-20736123

RESUMEN

PURPOSE: Bupivacaine myotoxicity to the extraocular muscles, from retrobulbar or peribulbar anesthesia, has been reported after cataract surgery and other intraocular procedures. However, there are no data on the concentration-dependence of bupivacaine in causing extraocular muscle toxicity. METHODS: Six aged rabbits received different concentrations of bupivacaine (0.75% and lower) in 3 extraocular muscles, namely, superior rectus, inferior rectus, and inferior oblique muscles of each rabbit's eye. The animals were euthanized at 5 days or 1 month after the injections. Hematoxylin and eosin- and Masson trichrome-stained sections were obtained from the involved extraocular muscles after paraffin embedding. RESULTS: Five days after the initial injection, the 0.75% bupivacaine-injected extraocular muscles showed extensive myonecrosis and degeneration with early-stage regenerating muscle fibers. However, muscle tissue injected with half-concentration bupivacaine (0.38%) showed scattered and significantly fewer areas of mild muscle fiber degeneration with regeneration. There were no areas of muscle tissue degeneration observed in any muscle injected with quarter-concentration bupivacaine (0.19%). At 1 month, however, only 0.75% bupivacaine-injected muscles displayed areas of regenerated muscle fiber cells with foci of scar formation. There was no visible scar formation in muscles injected with any bupivacaine concentration lower than 0.75%, or with saline, at 1 month after injection. CONCLUSIONS: Extraocular muscle injection with full-strength bupivacaine (0.75%) can cause myonecrosis and degeneration acutely, with regeneration appearing by 5 days, followed by some late-stage scar formation. However, no long-term effects were observed with bupivacaine concentrations of 0.38% or 0.19%.


Asunto(s)
Bupivacaína/toxicidad , Músculos Oculomotores/efectos de los fármacos , Anestésicos Locales/administración & dosificación , Anestésicos Locales/toxicidad , Animales , Bupivacaína/administración & dosificación , Modelos Animales de Enfermedad , Relación Dosis-Respuesta a Droga , Estudios de Seguimiento , Inyecciones Intramusculares , Necrosis/inducido químicamente , Necrosis/patología , Músculos Oculomotores/patología , Músculos Oculomotores/fisiopatología , Conejos
18.
Melanoma Res ; 20(2): 126-32, 2010 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-20061986

RESUMEN

This study evaluated the expression profile of hepatocyte growth factor (HGF), c-Met, epidermal growth factor receptor (EGFR), insulin-like growth factor-1 receptor (IGF-1R), and vitreal and serum EGF, HGF, IGF-1 levels in patients with uveal melanoma and assessed their correlation with the clinicopathological parameters. Forty patients with uveal melanoma were included in the study. Clinicopathological parameters were evaluated with hematoxylin-eosin staining. HGF, c-Met, EGFR, and IGF-1R expressions were evaluated immunohistochemically. HGF, EGF, and IGF-1 levels were measured with enzyme-linked immunosorbent assay in vitreous and serum specimens taken at enucleation and 6 months after the enucleation. HGF, c-Met, IGF-1R, and EGFR expressions were detected in 57.5, 20, 20, and 12.5% of cases, respectively. IGF-1R expression was significantly correlated with the degree of pigmentation, necrosis, and lymphocyte infiltration (P=0.013, 0.04, and 0.017). EGFR expression was significantly correlated with the mitosis rate (P=0.02). Vitreal EGF and serum IGF-1 levels were significantly higher in patients with scleral invasion (15.72+/-29.13, 199.01+/-154.01 pg/ml, respectively) when compared with the patients without invasion (0.56+/-1.05, 33.01+/-36.52 pg/ml) (P=0.03 and 0.015). When the preoperative and postoperative serum growth factor levels were compared, the serum EGF level was found to be lower (125.93+/-62.84, 100.02+/-31.19 pg/ml, P=0.007) and the serum IGF-1 level (165.81+/-153.6, 301.35+/-131.24 pg/ml, P<0.001) was found to be higher in the postoperative 6-month specimens. Uveal melanomas express HGF, c-Met, EGFR, and IGF-1R. Vitreal growth factor levels and expression of EGFR and IGF-1R are correlated with some clinicopathological parameters. IGF-1 and EGF may have a role in the development and progression of uveal melanoma.


Asunto(s)
Receptores ErbB/metabolismo , Factor de Crecimiento de Hepatocito/metabolismo , Melanoma/metabolismo , Proteínas Proto-Oncogénicas c-met/metabolismo , Receptor IGF Tipo 1/metabolismo , Neoplasias de la Úvea/metabolismo , Adulto , Anciano , Anciano de 80 o más Años , Biomarcadores de Tumor/genética , Biomarcadores de Tumor/metabolismo , Ensayo de Inmunoadsorción Enzimática , Receptores ErbB/genética , Femenino , Factor de Crecimiento de Hepatocito/genética , Humanos , Inmunohistoquímica , Masculino , Melanoma/genética , Melanoma/patología , Persona de Mediana Edad , Proteínas Proto-Oncogénicas c-met/genética , Receptor IGF Tipo 1/genética , Neoplasias de la Úvea/genética , Neoplasias de la Úvea/patología
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