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1.
Artigo em Alemão | MEDLINE | ID: mdl-29797014

RESUMO

The International Classification of Functioning, Disability and Health (ICF) provides a standardized language of almost 1500 ICF categories for coding information about functioning and contextual factors. Short lists (ICF Core Sets) are helpful tools to support the implementation of the ICF in clinical routine. In this paper we report on the implementation of ICF Core Sets in clinical routine using the "ICF Core Sets for Hand Conditions" and the "Lighthouse Project Hand" as an example. Based on the ICF categories of the "Brief ICF Core Set for Hand Conditions", the ICF-based assessment tool (ICF HandA) was developed aiming to guide the assessment and treatment of patients with injuries and diseases located at the hand. The ICF HandA facilitates the standardized assessment of functioning - taking into consideration of a holistic view of the patients - along the continuum of care ranging from acute care to rehabilitation and return to work. Reference points for the assessment of the ICF HandA are determined in treatment guidelines for selected injuries and diseases of the hand along with recommendations for acute treatment and care, procedures and interventions of subsequent treatment and rehabilitation. The assessment of the ICF HandA according to the defined reference points can be done using electronic clinical assessment tools and allows for an automatic generation of a timely medical report of a patient's functioning. In the future, the ICF HandA can be used to inform the coding of functioning in ICD-11.


Assuntos
Traumatismos da Mão/classificação , Classificação Internacional de Doenças , Classificação Internacional de Funcionalidade, Incapacidade e Saúde , Guias de Prática Clínica como Assunto , Avaliação da Deficiência , Pessoas com Deficiência , Alemanha , Mãos/fisiopatologia , Traumatismos da Mão/fisiopatologia , Humanos , Avaliação de Resultados em Cuidados de Saúde
2.
Toxicol Lett ; 293: 62-66, 2018 Sep 01.
Artigo em Inglês | MEDLINE | ID: mdl-29191789

RESUMO

The clinical progression following a sulfur mustard-induced skin exposure is well documented in the literature. Upon skin contact and a characteristic latency period, sulfur mustard (SM) causes erythema, blister formation and ulceration, which is associated with wound healing disorders that may require surgical treatment. Here, we present a case report of accidental exposure to SM in a laboratory setting which required surgical treatment of the skin. The case was illustrated at close intervals over a period of two years and underlines that exposure to SM has to be taken into account when typical clinical symptoms occur. Moreover skin grafts appear to be effective in SM-induced non healing skin ulcerations.


Assuntos
Substâncias para a Guerra Química/intoxicação , Gás de Mostarda/intoxicação , Acidentes , Adulto , Vesícula/patologia , Eritema/patologia , Humanos , Masculino , Exposição Ocupacional , Pele/patologia , Transplante de Pele/métodos , Úlcera Cutânea/induzido quimicamente , Úlcera Cutânea/patologia , Úlcera Cutânea/cirurgia
3.
J Hand Surg Am ; 42(4): 274-284, 2017 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-28372640

RESUMO

Management of fingertip and thumb tip injuries has recently undergone substantial changes. The time-proven traditional armamentarium of local flaps has been expanded and replaced by a wide variety of flaps. Simultaneous with the development of new flaps, the conservative treatment of fingertip and thumb tip injuries with semiocclusive dressings has also become a more acceptable treatment for these injuries. The excellent results with respect to restoring contour, sensibility of the pulp, and aesthetics of the finger justify this more tedious and time-consuming treatment of fingertip and thumb tip injuries. This article gives an update of the most commonly used flaps and the semiocclusive dressing treatments of fingertip and thumb tip injuries.


Assuntos
Traumatismos dos Dedos/cirurgia , Curativos Oclusivos , Procedimentos de Cirurgia Plástica/métodos , Lesões dos Tecidos Moles/cirurgia , Retalhos Cirúrgicos , Algoritmos , Desbridamento , Estética , Humanos , Recuperação de Função Fisiológica , Sensação , Retalhos Cirúrgicos/irrigação sanguínea , Retalhos Cirúrgicos/cirurgia , Polegar/lesões , Polegar/cirurgia
4.
Patient ; 10(3): 367-376, 2017 06.
Artigo em Inglês | MEDLINE | ID: mdl-28005235

RESUMO

BACKGROUND: The Disabilities of the Arm, Shoulder and Hand (DASH) Questionnaire is the most commonly applied patient-reported outcome measure used to assess disability and functioning in clinical research and practice for patients with injuries and diseases of the upper extremities. The objective of this study was to assess whether the DASH is a valid and reliable questionnaire to measure disability and functioning in patients with hand injuries and diseases using Rasch analysis. METHODS: We performed a psychometric study using data derived from two multicentre studies carried out to develop the International Classification of Functioning, Disability and Health (ICF) Core Sets for Hand Conditions. We analysed the data of 417 patients recruited in a clinical setting and suffering from hand injuries (e.g. finger fracture, flexor tendon injury) or diseases (e.g. carpal tunnel syndrome, rhizarthrosis). We examined whether the DASH fulfilled the assumptions for its use as a measure by applying a partial credit model and testing for differential item functioning for sex and age. RESULTS: Bifactor analysis revealed problems with the underlying latent trait of functioning and disability. Rasch analysis raised further issues, including disordered thresholds for eight items and misfit in nine items. One item showed Differential Item Functioning for sex. CONCLUSION: The study reveals that some DASH items do not fit the underlying trait that the DASH aims to measure. Further studies using Rasch analysis are needed to compare our findings with results of studies involving other target groups (e.g. patients with injuries of the upper arm and shoulder).


Assuntos
Avaliação da Deficiência , Traumatismos da Mão/reabilitação , Artropatias/reabilitação , Inquéritos e Questionários/normas , Adulto , Braço , Feminino , Lateralidade Funcional , Mãos , Indicadores Básicos de Saúde , Humanos , Masculino , Pessoa de Meia-Idade , Psicometria , Reprodutibilidade dos Testes , Ombro , Fatores Socioeconômicos
5.
Toxicol Lett ; 244: 112-120, 2016 Feb 26.
Artigo em Inglês | MEDLINE | ID: mdl-26321678

RESUMO

Sulfur mustard (SM) is a chemical warfare agent (CWA) that was first used in World War I and in several military conflicts afterwards. The threat by SM is still present even today due to remaining stockpiles, old and abandoned remainders all over the world as well as to its ease of synthesis. CWA are banned by the Chemical Weapons Convention (CWC) interdicting their development, production, transport, stockpiling and use and are subjected to controlled destruction. The present case report describes an accidental exposure of three workers that occurred during the destruction of SM. All exposed workers presented a characteristic SM-related clinical picture that started about 4h after exposure with erythema and feeling of tension of the skin at the upper part of the body. Later on, superficial blister and a burning phenomenon of the affected skin areas developed. Similar symptoms occurred in all three patients differing severity. One patient presented sustained skin affections at the gluteal region while another patient came up with affections of the axilla and genital region. Fortunately, full recovery was observed on day 56 after exposure except some little pigmentation changes that were evident even on day 154 in two of the patients. SM-exposure was verified for all three patients using bioanalytical GC MS and LC MS/MS based methods applied to urine and plasma. Urinary biotransformation products of the ß-lyase pathway were detected until 5 days after poisoning whereas albumin-SM adducts could be found until day 29 underlining the beneficial role of adduct detection for post-exposure verification. In addition, we provide general recommendations for management and therapy in case of SM poisoning.


Assuntos
Acidentes , Vesícula/induzido quimicamente , Substâncias para a Guerra Química/intoxicação , Documentação , Eritema/induzido quimicamente , Irritantes/intoxicação , Gás de Mostarda/intoxicação , Pele/efeitos dos fármacos , Adulto , Vesícula/diagnóstico , Vesícula/terapia , Substâncias para a Guerra Química/metabolismo , Cromatografia Líquida , Eritema/diagnóstico , Eritema/terapia , Cromatografia Gasosa-Espectrometria de Massas , Humanos , Masculino , Pessoa de Meia-Idade , Gás de Mostarda/metabolismo , Intoxicação/diagnóstico , Intoxicação/terapia , Ligação Proteica , Indução de Remissão , Albumina Sérica/metabolismo , Albumina Sérica Humana , Índice de Gravidade de Doença , Pele/patologia , Espectrometria de Massas em Tandem , Fatores de Tempo , Resultado do Tratamento
6.
Bioorg Med Chem Lett ; 25(16): 3275-80, 2015 Aug 15.
Artigo em Inglês | MEDLINE | ID: mdl-26105194

RESUMO

Although overweight and obesity are highly prevalent conditions, options to treat them are still very limited. As part of our search for safe and effective MCH-R1 antagonists for the treatment of obesity, two series of pyridones and pyridazinones were evaluated. Optimization was aimed at improving DMPK properties by increasing metabolic stability and improving the safety profile by reducing inhibition of the hERG channel and reducing the potential to induce phospholipidosis. Steric shielding of a labile keto moiety with an ortho-methyl group and fine-tuning of the polarity in several parts of the molecule resulted in BI 186908 (11 g), a potent and selective MCH-R1 antagonist with favorable DMPK and CMC properties. Chronic administration of BI 186908 resulted in significant body weight reduction comparable to sibutramine in a 4 week diet-induced obesity model in rats. Based on its favorable safety profile, BI 186908 was advanced to pre-clinical development.


Assuntos
Fármacos Antiobesidade/síntese química , Fármacos Antiobesidade/farmacologia , Piridazinas/síntese química , Piridazinas/farmacologia , Piridinas/síntese química , Piridinas/farmacologia , Receptores de Somatostatina/antagonistas & inibidores , Animais , Depressores do Apetite/farmacologia , Peso Corporal/efeitos dos fármacos , Ciclobutanos/farmacologia , Descoberta de Drogas , Canais de Potássio Éter-A-Go-Go/antagonistas & inibidores , Hepatócitos/metabolismo , Ensaios de Triagem em Larga Escala , Humanos , Técnicas In Vitro , Lipidoses/tratamento farmacológico , Microssomos Hepáticos/metabolismo , Fosfolipídeos/metabolismo , Bloqueadores dos Canais de Potássio/síntese química , Bloqueadores dos Canais de Potássio/farmacologia , Pirazinas/síntese química , Pirazinas/farmacologia , Ratos , Relação Estrutura-Atividade
7.
Bioorg Med Chem Lett ; 25(16): 3264-9, 2015 Aug 15.
Artigo em Inglês | MEDLINE | ID: mdl-26112443

RESUMO

Despite recent approvals of anti-obesity drugs there is still a high therapeutic need for alternative options with higher efficacy in humans. As part of our MCH-R1 antagonist program for the treatment of obesity, a series of biphenylacetamide HTS hits was evaluated. Several issues of the initial lead structures had to be resolved, such as potency, selectivity over related GPCRs and P-gp efflux limiting brain exposure in this series. We could demonstrate that all parameters can be significantly improved by structural modifications resulting in BI 414 as a potent and orally available MCH-R1 antagonist tool compound with acceptable in vivo efficacy in an animal model of obesity.


Assuntos
Alcinos/síntese química , Alcinos/farmacologia , Fármacos Antiobesidade/síntese química , Fármacos Antiobesidade/farmacologia , Piridinas/síntese química , Piridinas/farmacologia , Receptores de Somatostatina/antagonistas & inibidores , Membro 1 da Subfamília B de Cassetes de Ligação de ATP/metabolismo , Animais , Peso Corporal/efeitos dos fármacos , Citocromo P-450 CYP2D6/metabolismo , Inibidores das Enzimas do Citocromo P-450/síntese química , Inibidores das Enzimas do Citocromo P-450/farmacologia , Desenho de Fármacos , Ingestão de Alimentos/efeitos dos fármacos , Ensaios de Triagem em Larga Escala , Obesidade/tratamento farmacológico , Ratos , Receptores Acoplados a Proteínas G/efeitos dos fármacos , Receptores Acoplados a Proteínas G/metabolismo , Relação Estrutura-Atividade
8.
Bioorg Med Chem Lett ; 25(16): 3270-4, 2015 Aug 15.
Artigo em Inglês | MEDLINE | ID: mdl-26077492

RESUMO

Despite recent success there remains a high therapeutic need for the development of drugs targeting diseases associated with the metabolic syndrome. As part of our search for safe and effective MCH-R1 antagonists for the treatment of obesity, a series of 3,6-disubstituted pyridazines was evaluated. During optimization several issues of the initial lead structures had to be resolved, such as selectivity over related GPCRs, inhibition of the hERG channel as well as the potential to induce phospholipidosis. Utilizing property-based design, we could demonstrate that all parameters can significantly be improved by consequently increasing the polarity of the compounds. By this strategy, we succeeded in identifying potent and orally available MCH-R1 antagonists with good selectivity over M1 and 5-HT2A and an improved safety profile with respect to hERG inhibition and phospholipidosis.


Assuntos
Fármacos Antiobesidade/síntese química , Canais de Potássio Éter-A-Go-Go/antagonistas & inibidores , Lipidoses/tratamento farmacológico , Fosfolipídeos/metabolismo , Bloqueadores dos Canais de Potássio/síntese química , Bloqueadores dos Canais de Potássio/farmacologia , Piridazinas/síntese química , Piridazinas/farmacologia , Receptores de Somatostatina/antagonistas & inibidores , Animais , Fármacos Antiobesidade/farmacologia , Bloqueadores dos Canais de Potássio/farmacocinética , Piridazinas/farmacocinética , Ratos , Ratos Wistar , Receptor 5-HT2A de Serotonina/efeitos dos fármacos , Antagonistas da Serotonina/síntese química , Antagonistas da Serotonina/farmacologia , Relação Estrutura-Atividade
9.
J Hand Surg Am ; 40(3): 614-22; quiz 623, 2015 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-25708438

RESUMO

The management of thumb tip injuries has undergone great changes in recent years. The traditional armamentarium of flaps has been expanded and replaced by a wide variety of flaps with more versatility and less donor side morbidity. Parallel to the development of new flaps, the conservative treatment of thumb tip injuries with semi-occlusive dressing has gained ground in the treatment of these injuries. Although tedious and time-consuming, and requiring intensive communication with the patient to explain the look and occasionally fetid smell of the wound, this technique yields excellent results with respect to restoring contour and sensibility in pulp injuries. The article gives an update on the current options for treating thumb tip injuries including the most commonly applied flaps.


Assuntos
Traumatismos dos Dedos/cirurgia , Procedimentos de Cirurgia Plástica/métodos , Lesões dos Tecidos Moles/cirurgia , Retalhos Cirúrgicos/transplante , Polegar/lesões , Desbridamento/métodos , Educação Médica Continuada , Feminino , Traumatismos dos Dedos/diagnóstico , Rejeição de Enxerto , Sobrevivência de Enxerto , Humanos , Escala de Gravidade do Ferimento , Masculino , Curativos Oclusivos , Prognóstico , Recuperação de Função Fisiológica , Medição de Risco , Lesões dos Tecidos Moles/diagnóstico , Retalhos Cirúrgicos/irrigação sanguínea , Polegar/cirurgia , Resultado do Tratamento , Cicatrização/fisiologia
10.
J Hand Ther ; 26(4): 332-42; quiz 342, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-23911076

RESUMO

STUDY DESIGN: Qualitative study. INTRODUCTION: Clinical outcome evaluation needs to consider the patient perspective for an in-depth understanding of functioning and disability. PURPOSE OF THE STUDY: To explore whether patient-reported outcome measures (PROMs) used in the field of hand injuries or hand disorders, capture functioning aspects and environmental factors important to the patients. METHODS: We performed a qualitative study and a systematic literature review. The focus group sessions were recorded, transcribed verbatim, and the identified concepts were linked to the ICF. We searched in MEDLINE for reviews, related to injuries or disorders of the hand, reporting on PROMs. We linked the items of the identified PROMs to the ICF and compared the qualitative data with the content of the PROMs. RESULTS: Statements from 45 individuals who participated in eight focus groups were linked to 97 categories of the ICF. From 15 reviews included, eight PROMs were selected. The selected PROMs capture 34 of the categories retrieved from the qualitative data. CONCLUSIONS: PROMs used in the context of hand injuries or hand disorders capture only in parts the functioning aspects important to the patients.


Assuntos
Traumatismos da Mão/terapia , Avaliação de Resultados em Cuidados de Saúde , Síndrome do Túnel Carpal/terapia , Contratura de Dupuytren/terapia , Grupos Focais , Traumatismos da Mão/fisiopatologia , Humanos , Psicometria , Pesquisa Qualitativa , Recuperação de Função Fisiológica , Sensação
11.
Disabil Rehabil ; 34(8): 681-93, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-21978202

RESUMO

PURPOSE: A formal decision-making and consensus process was applied to develop the first version of the International Classification on Functioning, Disability and Health (ICF) Core Sets for Hand Conditions. METHOD: To convene an international panel to develop the ICF Core Sets for Hand Conditions (HC), preparatory studies were conducted, which included an expert survey, a systematic literature review, a qualitative study and an empirical data collection process involving persons with hand conditions. A consensus conference was convened in Switzerland in May 2009 that was attended by 23 healthcare professionals, who treat hand conditions, representing 22 countries. RESULTS: The preparatory studies identified a set of 743 ICF categories at the second, third or fourth hierarchical level. Altogether, 117 chapter-, second-, or third-level categories were included in the comprehensive ICF Core Set for HC. The brief ICF Core Set for HC included a total of 23 chapter- and second-level categories. CONCLUSIONS: A formal consensus process integrating evidence and expert opinion based on the ICF led to the formal adoption of the ICF Core Sets for Hand Conditions. The next phase of this ICF project is to conduct a formal validation process to establish its applicability in clinical settings.


Assuntos
Avaliação da Deficiência , Mãos/fisiopatologia , Indicadores Básicos de Saúde , Classificação Internacional de Doenças , Atividades Cotidianas/classificação , Conferências de Consenso como Assunto , Pessoas com Deficiência/classificação , Prova Pericial , Pessoal de Saúde , Humanos , Suíça , Organização Mundial da Saúde
12.
Bioorg Med Chem Lett ; 20(4): 1410-4, 2010 Feb 15.
Artigo em Inglês | MEDLINE | ID: mdl-20096576

RESUMO

Compound 4p was identified from a series of 6-hydroxy-4H-benzo[1,4]oxazin-3-ones as potent agonist of the human beta2-adrenoceptor with a high beta1/beta2-selectivity. A complete reversal of acetylcholine-induced bronchoconstriction which lasted over the whole study period of 5h was demonstrated for 4p in a guinea pig in vivo model without any signs of cardiovascular effects up to 10-fold above the first dose reaching 100% bronchoprotection. The enantiomerically pure (R)-form of 4p exerted a bronchodilatory efficacy over 24 h in dogs and guinea pigs in the absence of systemic pharmacodynamic effects. Formoterol which was tested as comparator in the same in vivo models of acetylcholine-induced bronchoconstriction did not retain efficacy after 24 h. In summary, the preclinical profile of compound (R)-4p (olodaterol, also known as BI 1744 CL) suggests a potential for once-daily dosing in man accompanied with an improved safety profile.


Assuntos
Agonistas de Receptores Adrenérgicos beta 2 , Benzoxazinas/química , Benzoxazinas/farmacologia , Broncodilatadores/química , Administração por Inalação , Animais , Benzoxazinas/síntese química , Broncodilatadores/administração & dosagem , Broncodilatadores/farmacologia , Células CHO , Cricetinae , Cricetulus , Cães , Cobaias , Humanos , Masculino , Estrutura Molecular , Proteínas Recombinantes/genética , Estereoisomerismo , Resultado do Tratamento
13.
Bioorg Med Chem Lett ; 19(23): 6640-4, 2009 Dec 01.
Artigo em Inglês | MEDLINE | ID: mdl-19875286

RESUMO

Novel beta(2)-agonists with a 5-hydroxy-4H-benzo[1,4]oxazin-3-one moiety as head group are described. Systematic chemical variations at the phenethylamine residue of these compounds lead to the discovery of compound 6m as potent, full agonist of the beta(2)-adrenoceptor with a high beta(1)/beta(2)-selectivity. Molecular modeling revealed an interaction between the carboxylic acid group of 6m and a lysine residue (K305) of the beta(2)-receptor as putative explanation for the high observed selectivity. Further, compound 6m displayed in a guinea pig in vivo model a complete reversal of acetylcholine induced bronchoconstriction which lasted over the complete study time of 5h.


Assuntos
Agonistas de Receptores Adrenérgicos beta 2 , Benzoxazinas/farmacologia , Benzoxazinas/síntese química , Benzoxazinas/química , Desenho de Fármacos , Modelos Moleculares , Estrutura Molecular , Estereoisomerismo , Relação Estrutura-Atividade
14.
Bioorg Med Chem Lett ; 19(17): 5237-40, 2009 Sep 01.
Artigo em Inglês | MEDLINE | ID: mdl-19643607

RESUMO

Beta2-adrenoceptor agonists with basic and acidic groups attached via an alkyl linker to the phenyl ethanolamine core were prepared and investigated in vitro and in vivo. The compounds exhibited a high potency in a functional cellular assay and a bronchoprotective effect in a guinea pig model which lasted over the complete study period of 5h.


Assuntos
Agonistas de Receptores Adrenérgicos beta 2 , Broncodilatadores/química , Etanolaminas/química , Agonistas de Receptores Adrenérgicos beta 1 , Animais , Asma/tratamento farmacológico , Broncodilatadores/síntese química , Broncodilatadores/farmacologia , Etanolaminas/síntese química , Etanolaminas/farmacologia , Cobaias , Frequência Cardíaca , Humanos , Receptores Adrenérgicos beta 1/metabolismo , Receptores Adrenérgicos beta 2/metabolismo
15.
Eur J Trauma Emerg Surg ; 35(6): 527-31, 2009 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-26815375

RESUMO

Open tibial fractures usually result from high-energy trauma. Severe soft-tissue injuries are often combined with open fractures of the distal tibia. A consecutive series of 42 patients with open extraarticular distal tibial fractures (Gustilo I-IIIc) operated on between July 2006 and February 2009 were included in the study reported here. We performed open reduction and internal fixation for the Gustilo I cases. Soft tissue was closed directly after antibiotic beads had been temporarily applied. For the Gustilo II and III cases, our treatment protocol included soft-tissue debridement of all devitalized soft tissue and bone fragments, pulsatile jet irrigation, and external stabilization. Soft tissue was temporarily closed with Epigard_ after the application of antibiotic beads. A second-look operation was scheduled after 3-5 days. Gustilo II patients needed an average of 1.1 (0-3) revisions until wound closure, compared to the average of 2.1 revisions necessary for the Gustilo III patients. It took 5.6 (0-16) days to obtain definitive wound closure in the Gustilo II patients and 9.9 (3-28) days in the Gustilo III patients. Skin grafting was sufficient for definitive softtissue closure in ten cases, local flaps in eight cases, and free musculocutaneous flaps were needed in six cases. Gustilo II patients with primary wound closure remained hospitalized for 11 days, while patients with secondary wound closure stayed in hospital for an average of 20 days. Our early results concerning infection rate, number of reoperations, and time to bony consolidation can be compared with other studies. Functional results will have to be evaluated at clinical follow-up.

16.
Opt Express ; 16(16): 12239-50, 2008 Aug 04.
Artigo em Inglês | MEDLINE | ID: mdl-18679501

RESUMO

The conception and realization of an imaging microspectrometer, limited to an optical volume of 11 x 6 x 5 mm(3), is presented. The spectrometer is based on a multi-order concept and offers an overall spectral bandwidth of 400-1030 nm with better than 2.5 nm resolution in the visible range. The numerical aperture of NA = 0.2 allows an appropriate energy efficiency. As the most essential element of the microspectrometer, a concave diffraction grating with a diameter of 5 mm and an image distance of f = 8.6 mm was manufactured in a holographic recording process. For the recording process the specifications of the concave grating require two diffraction limited point sources in very close proximity. To provide a point source distance below 1 mm a recording concept based on the introduction of a supplementary hologram was employed.


Assuntos
Desenho Assistido por Computador , Holografia/instrumentação , Modelos Teóricos , Refratometria/instrumentação , Análise Espectral/instrumentação , Simulação por Computador , Desenho de Equipamento , Análise de Falha de Equipamento , Miniaturização
17.
Trends Pharmacol Sci ; 28(11): 580-7, 2007 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-17963849

RESUMO

Migraine is a complex, debilitating neurovascular disorder. Although knowledge on the main molecular players is still incomplete, recent preclinical and clinical findings indicate that there is a clear correlation between migraine-associated headache and the release of the neuropeptide calcitonin gene-related peptide (CGRP). BIBN4096 was the first CGRP antagonist to be tested in clinical trials for the treatment of migraine. The proven efficacy of this agent, and also the CGRP antagonist MK-0974, to alleviate acute migraine headache provided significant support for the hypothesis that CGRP has an important role in migraine pathophysiology. Moreover, the recently published results from Phase II trials are encouraging and suggest that this new type of drug might offer advantages over existing therapies for patients suffering from migraine and related headaches.


Assuntos
Peptídeo Relacionado com Gene de Calcitonina/antagonistas & inibidores , Transtornos de Enxaqueca/tratamento farmacológico , Animais , Azepinas/química , Azepinas/farmacologia , Azepinas/uso terapêutico , Peptídeo Relacionado com Gene de Calcitonina/fisiologia , Ensaios Clínicos como Assunto , Dipeptídeos/química , Dipeptídeos/farmacologia , Dipeptídeos/uso terapêutico , Humanos , Imidazóis/química , Imidazóis/farmacologia , Imidazóis/uso terapêutico , Transtornos de Enxaqueca/fisiopatologia , Modelos Biológicos , Estrutura Molecular , Quinazolinas/química , Quinazolinas/farmacologia , Quinazolinas/uso terapêutico
18.
J Med Chem ; 48(19): 5921-31, 2005 Sep 22.
Artigo em Inglês | MEDLINE | ID: mdl-16161996

RESUMO

Although the triptans have greatly improved the acute treatment of migraine headache, there are yet many shortcomings. Therefore, new strategies for the treatment of migraine are needed which offer advantages over current therapy, e.g. triptans. Our novel approach was based on the hypothesis that the release of calcitonin gene-related peptide (CGRP) could play a causative role in migraine headache. Thus we initiated a program aimed at the design and synthesis of small molecule CGRP receptor antagonists. High throughput screening led to the identification of (R)-Tyr-(S)-Lys dipeptide-like compounds that showed weak but unequivocal binding to the human CGRP receptor. Lead optimization afforded highly potent CGRP antagonists, the prototype being compound 19 (BIBN4096). This compound exhibiting a favorable biological profile was selected for initial clinical trials. A proof of concept study indicated that intravenous application of 19 was effective in the treatment of acute migraine headache. This finding strongly supports our initial working hypothesis that CGRP plays an important role in the pathophysiology of migraine.


Assuntos
Antagonistas do Receptor do Peptídeo Relacionado ao Gene de Calcitonina , Dipeptídeos/síntese química , Transtornos de Enxaqueca/tratamento farmacológico , Quinazolinas/síntese química , Doença Aguda , Animais , Callithrix , Linhagem Celular Tumoral , AMP Cíclico/biossíntese , Dipeptídeos/química , Dipeptídeos/farmacologia , Humanos , Técnicas In Vitro , Quinazolinas/química , Quinazolinas/farmacologia , Ratos , Baço/metabolismo , Relação Estrutura-Atividade
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