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Uloga inhibitora vaskularnog endotelnog faktora rasta u terapiji dijabetičnog makularnog edema / The role of an inhibitor of vascular endothelial growth factor in the treatment of diabetic macular edemaJovanović Sandra 25 March 2015 (has links)
<p>Dijabetesna retinopatija je među vodećim uzročnicima stečenog slepila, kako u razvijenim zemljama, tako i zemljama u razvoju. Dijabetesna retinopatija je jedna od<br />najčešćih komplikacija Dijabetes Mellitus-a. U sklopu dijabetesne retinopatije jedan od najranijih razloga koji dovodi do pada vidne oštrine je dijabetični makularni edem (DME). Pad vidne oštrine kod pacijenata sa dijabetesom narušava njihov kvalitet života i umanjuje radnu sposobnost. Dosadašnji oblik lečenja laserfotokoaguacijom makule, nije dao zadovoljavajuće rezultate. U novije vreme sve više je zastupljeno farmakološko lečenje edema koje podrazumeva intrvitrealnu aplikaciju lekova iz grupe inhibitora vaskularnog endotelnog faktora rasta (VEGF inhibitori), koji dovodi do stabilizacije zidova krvnih sudova. <br />Cilj ove studije je da se ispita efikasnost lečenja DME uz pomoć intravitrealno aplikovanih lekova iz grupe inhibitora vaskularnog endotelnog faktora rasta u odnosu na konvencionalno do sada priznato lečenje laserfotokogulacijom makule. <br />Efikasnost lečenja je procenjivana na dva načina: anatomski, na osnovu smanjenja centralne makularne debljine izražene u μm, merene metodom optičke koherentne tomografije, i funkcionalno, na osnovu poboljšanja vidne oštrine koja je izražavana u log MAR jedinicama. U ovoj prospektivnoj, randomiziranoj kliničkoj studiji sa minimumom praćenja od 6 meseci, u eksperimentalnoj grupi tretiran je 51 pacijent,<br />odnosno 84 oka aplikacijom bevacizumaba (anti VEGF agens) u dozi od 1,25 mg, sa ili bez dodatnog laser tretmana. <br />Uz prosečno 2,46 inekcije postignuta je prosečna redukcija centralne makularne debljine od 139,15 μm. Dobijene vrednosti su nakon svake aplikovane doze su značajno bolje u odnosu na početnu. Edemi sa većom centralnom makularnom debljinom su zahtevali tretman sa većim brojem inekcija. Kod većih edema je postignuta i veća redukcija centralne makularne debljine. U odnosu na vidnu oštrinu u eksperimentalnoj grupi postignuto je poboljšanje od 0,135 log MAR jedinica. Efekat lasera kao samostalne terapije u kontrolnoj grupi (50 pacijenata, 92 oka) nije bio<br />značajan ni u pogledu smanjenja centralne makularne debljine kao ni na osnovu poboljšnja vidne oštrine. Tretman bevacizumabom samostalno ili u kombinaciji sa laserom je efikasniji u tretmanu DME u odnosu na konvencionalni tretman laserfotokoaguacijom koji potvrđeno dovodi do stabilizacije stanja. Značaj ove studije je potvrda efikasnosti i bezbednosti jednog novog oblika lečenja koji samostalno ili u kombinaciji sa laser tretmanom predstavlja novi protokol lečenja dijabetičnog makularnog edema.</p> / <p>Diabetic retinopathy is among the leading causes of acquired blindness in developed countries, as well as in developing countries. Diabetic retinopathy is one of the most frequent Diabetes Mellitus complications. Within diabetic retinopathy, diabetic macular edema (DME) is one of the earliest causes of the loss of visual acuity. Impaired vision causes decline in life quality in diabetic patients and it decreases their<br />working ability. Up to this date, laser photocoagulation treatment has not given<br />satisfactory results. Recently, new promising treatment forms have emerged, including the intravitreal application of vascular endothelium growth factor (VEGF inhibitors), which lead to stabilization of the vessel wall. The aim of this study is to evaluate the efficacy of DME treatment consisting of intravitreal VEGF inhibitor application alone or as a part of combined treatment (intravitreal VEGF inhibitor plus laser photocoagulation) compared with conventional laser treatment alone. The effect of treatment was evaluated according to morphological parameters by measuring central macular thickness (CMT) in μm with optical coherence tomography, and according to functional parameter by visual acuity in log MAR scale. In this prospective randomized clinical trial, with minimum follow up of 6 months, in experimental group 51 patient, or 84 eyes were treated with bevacizumab (VEGF inhibitor) in 1.25 mg dosage, alone or in combination with laser. The mean reduction in was 139.15 μm, which was achieved with 2.46 doses on average. The difference between the final and initial CMT values after each dos age was tatistically significant.<br />Edemas with high central macular thickness required high number of intraviteal<br />aplicatons and the reduction was higher. In our study, mean visual acuity improved significantly in 0.135 log MAR. In control group (50 patient, 92 eyes) treated with laserphotocolagulation alone, the effect on visual acuity and central acular thickness was not statistically significant. The treatment with bevacizumab alone or in combined<br />treatment is more effective in treating DME than conventional macular laser treatment alone, from both - anatomical and functional perspective. The importance of this study is confirmation of the efficacy and safety of a new form of treatment and the introduction of a new protocol for the treatment of diabetic macular edema.</p>
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Valor prognóstico das proteínas HIF-1α, VEGF e IL-8 em macerado tumoral mamário caninoFerreira, José Henrique Musumeci 20 October 2014 (has links)
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Previous issue date: 2014-10-20 / Introduction: Mammary neoplasms are the most common type of tumor in dogs. Some proteins play an important role in tumor progression, thus are candidate prognosis markers. During tumor growth, the transcription factor induced by hypoxia (HIF-1α) activates the expression of vascular endothelial growth factor (VEGF), promoting angiogenesis. Interleukin-8 (IL-8) is a pro-inflammatory and pro-angiogenic cytokine and has been associated with tumor progression. Objectives: To evaluate the prognostic value of HIF-1α, VEGF and IL-8 proteins in tumor tissue in dogs with mammary tumors, correlating them with clinicopathological parameters, clinical outcome and survival. Material and Methods: The concentrations of HIF-1α, VEGF and IL-8 proteins were evaluated by ELISA (Enzyme-linked immunosorbent) in macerated tumor of 25 bitches with mammary tumors and control samples and compared statistically. Results: The levels of HIF-1α, VEGF and IL-8 were higher in dogs over the age of 10 years and that had died (p <0.05). Moreover, HIF-1α concentrations were elevated in the tumors of dogs who developed metastases (p = 0.04), while VEGF levels were highest in tumors with clinical stages III and IV (p = 0.03) and IL-8 tumors in tumor with development greater than six months (p = 0.03). Still, high levels of HIF-1α, VEGF and IL-8 were also related to shorter overall survival (p <0.05). Conclusions: High levels of HIF-1α, VEGF and IL-8 are associated with features of poor prognosis, suggesting that the assessment of these proteins in tumor macerated has important prognostic value. / Introdução: As neoplasias mamárias são o tipo mais comum de tumor na espécie canina. Algumas proteínas exercem importante papel na progressão tumoral e portanto, são candidatos marcadores de prognóstico. Durante o crescimento tumoral, o fator de transcrição induzido por hipóxia (HIF-1α) ativa a expressão do fator de crescimento endotelial vascular (VEGF), promovendo a angiogênese. A interleucina-8 (IL-8) é uma citocina pró-inflamatória e pró-angiogênica e tem sido associada à progressão tumoral. Objetivos: Avaliar o valor prognóstico das proteínas HIF-1α, VEGF e IL-8 no tecido tumoral em cadelas com neoplasia mamária, relacionando-os com os parâmetros clínico-patológicos, evolução clínica e sobrevida. Material e Métodos: As concentrações das proteínas HIF-1α, VEGF e IL-8 foram avaliadas pelo método de ELISA (Enzyme-linked immunosorbent Assay) no macerado tumoral de 25 cadelas com neoplasia mamária e amostras controle e comparadas estatisticamente. Resultados: Os níveis de HIF-1α, VEGF e IL-8 foram maiores em cadelas com idade superior a 10 anos e que vieram a óbito (p < 0,05). Além disso, concentrações de HIF-1α foram elevadas nos tumores de cadelas que desenvolveram metástase (p = 0,04), enquanto os níveis de VEGF foram maiores em tumores com estadiamento clínico III e IV (p = 0,03), e de IL-8 em tumores com evolução tumoral maior que seis meses (p = 0,03). Ainda, níveis elevados de HIF-1α, VEGF e IL-8 também foram relacionados com menor tempo de sobrevida global (p < 0,05). Conclusões: Altas concentrações de HIF-1α, VEGF e IL-8 estão associadas com características de pior prognóstico, sugerindo que a avaliação dessas proteínas no macerado tumoral possui importante valor prognóstico.
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Mechanistic and therapeutic evaluation of a novel antiantiogenic small moleculeSulaiman, Rania S. 24 May 2016 (has links)
Indiana University-Purdue University Indianapolis (IUPUI) / Choroidal neovascularization (CNV) is the vision-threatening characteristic of wet
age-related macular degeneration (AMD), a major cause of blindness affecting
almost 2 million elderly Americans. The current approved treatments target the
dominant angiogenic mediator, vascular endothelial growth factor (VEGF).
However, repeated injections of anti-VEGF drugs can cause ocular and systemic
side effects, and about 30% of wet AMD patients are non-responsive. There is
thus an unmet need to develop VEGF-independent antiangiogenic molecules to
complement or combine with existing medications.
I studied SH-11037, a novel homoisoflavonoid with potent and selective
antiangiogenic activity against human retinal endothelial cells. Intravitreal SH-
11037 dose-dependently suppressed angiogenesis in the laser-induced CNV (LCNV)
mouse model. These effects were prominent as early as 7 days post-laser
treatment as measured by a novel ellipsoid quantification method of optical
coherence tomography images in vivo. A supratherapeutic dose of 100 μM SH-
11037 was not associated with signs of murine ocular toxicity, and did not
interfere with pre-existing retinal vasculature or retinal function. SH-11037
synergized with anti-VEGF therapy in vitro and in vivo, suggesting a VEGFindependent
mechanism. By photoaffinity pulldown, I identified soluble epoxide hydrolase (sEH) as an SH-11037-binding target. sEH is a key enzyme in ω-3 and
ω-6 fatty acid metabolism. sEH levels were dramatically upregulated in retinal
sections from L-CNV mice and a specific sEH inhibitor, t-AUCB, significantly
suppressed L-CNV lesion volume. Additionally, SH-11037 inhibited sEH
enzymatic activity in vitro and in vivo in L-CNV mice. Given the role of sEH in the
metabolism of docosahexaenoic acids (DHA), inhibition of sEH using small
molecules like SH-11037 would enhance ocular DHA levels, with beneficial
antiangiogenic and anti-inflammatory effects. SH-11037 is thus a novel sEH
inhibitor, which could make it an alternative or additive therapy to existing anti-
VEGF drugs for treatment of neovascular diseases in the eye and other tissues.
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