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1.
J Thromb Haemost ; 10(1): 49-55, 2012 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-22044645

RESUMO

AIMS: Blood cell infiltration and inflammation are involved in atrial remodelling during atrial fibrillation (AF) although the exact mechanisms of inflammatory cell recruitment remain poorly understood. Platelet-bound stromal cell-derived factor-1 (SDF-1) is increased in cases of ischemic myocardium and regulates recruitment of CXCR4(+) cells on the vascular wall. Whether platelet-bound SDF-1 expression is differentially influenced by non-valvular paroxysmal or permanent atrial fibrillation (AF) in patients with stable angina pectoris (SAP) or acute coronary syndrome (ACS) has not been reported so far. METHODS AND RESULTS: A total of 1291 consecutive patients with coronary artery disease (CAD) undergoing coronary angiography were recruited. Among the patients with SAP, platelet-bound-SDF-1 is increased in patients with paroxysmal AF compared with SR or to persistent/permanent AF (P < 0.05 for both). Platelet-bound SDF-1 correlated with plasma SDF-1 (r = 0.488, P = 0.013) in patients with AF and ACS, which was more pronounced among patients with persistent AF (r = 0.842, P = 0.009). Plasma SDF-1 was increased in persistent/permanent AF compared with SR. Patients with ACS presented with enhanced platelet-bound-SDF-1 compared with SAP. Interestingly, among patients with ACS, patients with paroxysmal or persistent/permanent AF presented with an impaired platelet-bound SDF-1 expression compared with patients with SR. CONCLUSIONS: Differential expression of platelet-bound and plasma SDF-1 was observed in patients with AF compared with SR which may be involved in progenitor cell mobilization and inflammatory cell recruitment in patients with AF and ischemic heart disease. Further in vivo studies are required to elucidate the role of SDF-1 in atrial remodeling and the atrial fibrillation course.


Assuntos
Fibrilação Atrial/sangue , Plaquetas/patologia , Quimiocina CXCL12/genética , Regulação da Expressão Gênica , Isquemia Miocárdica/sangue , Angina Estável , Plaquetas/metabolismo , Movimento Celular , Quimiocina CXCL12/análise , Humanos , Células-Tronco/patologia
2.
Cephalalgia ; 28(3): 226-36, 2008 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-18254893

RESUMO

We hypothesized that intravenous infusion of the parasympathetic transmitter, vasoactive intestinal peptide (VIP), might induce migraine attacks in migraineurs. Twelve patients with migraine without aura were allocated to receive 8 pmol kg(-1) min(-1) VIP or placebo in a randomized, double-blind crossover study. Headache was scored on a verbal rating scale (VRS), mean blood flow velocity in the middle cerebral artery (V(mean MCA)) was measured by transcranial Doppler ultrasonography, and diameter of the superficial temporal artery (STA) by high-frequency ultrasound. None of the subjects reported a migraine attack after VIP infusion. VIP induced a mild immediate headache (maximum 2 on VRS) compared with placebo (P = 0.005). Three patients reported delayed headache (3-11 h after infusion) after VIP and two after placebo (P = 0.89). V(mean MCA) decreased (16.3 +/- 5.9%) and diameter of STA increased significantly after VIP (45.9 +/- 13.9%). VIP mediates a marked dilation of cranial arteries, but does not trigger migraine attacks in migraineurs. These data provide further evidence against a purely vascular origin of migraine.


Assuntos
Transtornos de Enxaqueca/sangue , Transtornos de Enxaqueca/etiologia , Peptídeo Intestinal Vasoativo/toxicidade , Vasodilatação/efeitos dos fármacos , Vasodilatação/fisiologia , Adulto , Estudos Cross-Over , Método Duplo-Cego , Feminino , Humanos , Masculino , Transtornos de Enxaqueca/induzido quimicamente , Enxaqueca sem Aura , Peptídeo Intestinal Vasoativo/sangue , Vasodilatadores/sangue , Vasodilatadores/toxicidade
3.
Cephalalgia ; 27(11): 1265-70, 2007 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-17919305

RESUMO

The aim of this study was to provide data on the prognosis and treatment options of headache associated with sexual activity (HSA). Sixty patients diagnosed with HSA between 1996 and 2004 were followed up between 2003 and 2006 at least 12 months after the first interview. The further course of the disease and their contentedness with therapy were requested. On average, the second interview was performed 35.9 months after the first examination. Of the 45 patients who had suffered from single attacks or bouts prior to baseline examination, 37 had no further attacks. Seven patients suffered from at least one further bout with an average duration of 2.1 months. One patient developed a chronic course of the disease after an episodic start. Of the 15 patients with chronic disease at the first examination, seven were in remission and five had ongoing attacks at follow-up. Ten patients received indomethacin for preemptive therapy, with good results in nine patients. Eighteen patients received beta-blockers for prophylaxis, with good results in 15 patients. Episodic HSA occurs in approximately three-quarters and chronic HSA in approximately one-quarter of patients. Even in chronic HAS, the prognosis is favourable, with remission rates of 69% during an observation period of 3 years. For patients with longer-lasting bouts or with chronic HSA, prophylactic treatment with beta-blockers or preemptive therapy with indomethacin are often successful.


Assuntos
Antagonistas Adrenérgicos beta/uso terapêutico , Anti-Inflamatórios não Esteroides/uso terapêutico , Cefaleia/etiologia , Cefaleia/prevenção & controle , Comportamento Sexual , Adulto , Feminino , Seguimentos , Humanos , Indometacina/uso terapêutico , Masculino , Prognóstico
4.
Cephalalgia ; 26(8): 992-1003, 2006 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-16886936

RESUMO

The role of the parasympathetic nervous system in the pathogenesis of migraine is disputed. The headache-eliciting effect of the parasympathetic neurotransmitter, vasoactive intestinal polypeptide (VIP), and its effect on cerebral arteries and brain haemodynamics has not been systematically studied in man. We hypothesized that infusion of VIP might induce headache in healthy subjects and cause changes in cerebral haemodynamics. VIP (8 pmol/kg per min) or placebo (0.9% saline) was infused for 25 min into 12 healthy young volunteers in a crossover, double-blind design. Headache was scored on a verbal rating scale from 0 to 10, regional cerebral blood flow (rCBF) was measured with single-photon emission computed tomography and (133)Xe inhalation and mean flow velocity in the middle cerebral artery (V(meanMCA)) was measured with transcranial Doppler ultrasonography. The headache was very mild with a maximum score of 2 and described as a pressing or throbbing sensation. Five participants developed headache during VIP and one during placebo. During the infusion, a significant drop in V(meanMCA) was seen for VIP compared with placebo (P < 0.001), but the effect quickly waned and no difference was found when comparing the time between 30 and 120 min. In addition, no significant difference in the diameter of the MCA could be found during the infusion. No significant differences in rCBF (P = 0.10) were found between VIP and placebo. A marked dilation of the superficial temporal artery was seen (P = 0.04) after VIP in the first 30 min but no difference was found when comparing the time between 30 and 120 min. We found no difference in mean arterial blood pressure between VIP and placebo days but the heart rate increased significantly on a VIP day compared with a placebo day (AUC(0-30 min), P < 0.001). Plasma VIP was significantly higher on a VIP day compared with placebo (AUC(0-80 min), P < 0.001). These results show that VIP causes a decrease in V(meanMCA) without affecting rCBF. In spite of a marked vasodilator effect in the extracranial vessels and increased plasma VIP, healthy subjects developed only a very mild headache.


Assuntos
Cefaleia/induzido quimicamente , Cefaleia/diagnóstico , Medição da Dor/efeitos dos fármacos , Peptídeo Intestinal Vasoativo/administração & dosagem , Peptídeo Intestinal Vasoativo/toxicidade , Adulto , Relação Dose-Resposta a Droga , Método Duplo-Cego , Feminino , Cefaleia/classificação , Humanos , Masculino , Projetos Piloto , Efeito Placebo , Valores de Referência , Índice de Gravidade de Doença
5.
Neurology ; 67(3): 497-9, 2006 Aug 08.
Artigo em Inglês | MEDLINE | ID: mdl-16775229

RESUMO

The authors conducted a double-blind, placebo-controlled, crossover study to investigate the efficacy of oral zolmitriptan in the treatment of migraine in children and adolescents. Patients (n = 32) received placebo, zolmitriptan 2.5 mg, and ibuprofen 200 to 400 mg to treat three consecutive migraine attacks. Pain relief rates after 2 hours were 28% for placebo, 62% for zolmitriptan, and 69% for ibuprofen (p < 0.05). Both drugs are well tolerated with only mild side effects.


Assuntos
Ibuprofeno/uso terapêutico , Transtornos de Enxaqueca/tratamento farmacológico , Oxazolidinonas/uso terapêutico , Triptaminas/uso terapêutico , Administração Oral , Adolescente , Anti-Inflamatórios não Esteroides/administração & dosagem , Anti-Inflamatórios não Esteroides/uso terapêutico , Criança , Método Duplo-Cego , Feminino , Humanos , Ibuprofeno/efeitos adversos , Oxazolidinonas/efeitos adversos , Agonistas do Receptor de Serotonina/administração & dosagem , Agonistas do Receptor de Serotonina/uso terapêutico , Triptaminas/efeitos adversos
6.
Eur J Med Res ; 10(7): 305-8, 2005 Jul 29.
Artigo em Inglês | MEDLINE | ID: mdl-16055402

RESUMO

HIV infection can be associated with different types of arthropathies which are often underdiagnosed. We present the case of a 52 year old HIV positive man on highly active antiretroviral therapy including indinavir who developed an acute painful oligoarthritis. We present this case on HIV associated arthritis and include a review on other HIV specific types of arthritis (acute symmetric arthritis and painful articular syndrome) which are assumed as entities exclusively apparent in HIV patients. The pathophysiology of arthritis in HIV infected patients is not yet completely understood but a direct role of the HIV on the initiation of synovitis is suspected in some of them. Additionally, there is evidence that antiretroviral drugs, in particular the protease inhibitor indinavir, can lead to arthritic complications as well.


Assuntos
Artrite Infecciosa/etiologia , Infecções por HIV/complicações , Terapia Antirretroviral de Alta Atividade , Artrite Infecciosa/tratamento farmacológico , Artrite Infecciosa/patologia , Infecções por HIV/tratamento farmacológico , Infecções por HIV/patologia , Inibidores da Protease de HIV/uso terapêutico , Humanos , Indinavir/uso terapêutico , Masculino , Pessoa de Meia-Idade , Sinovite/patologia , Sinovite/virologia
7.
Fortschr Neurol Psychiatr ; 73(2): 74-82, 2005 Feb.
Artigo em Alemão | MEDLINE | ID: mdl-15685491

RESUMO

BACKGROUND AND PURPOSES: Aim of the study was to translate the original version of the Barthel-Index (BI) into German and to investigate the reliability of the German version. In addition, a German version of the BI for postal and telephone use was developed. METHODS: Data were collected in four neurological hospitals in Germany. The translation of the BI followed the protocol of the Medical Outcomes Trust. The interrater reliability of the German version of the BI was investigated in 72 patients after acute stroke. The reliability of the postal and telephone version of the BI was compared with face-to-face interview in 147 patients three months after stroke. Reliability was assessed using simple weighted kappa-statistics. RESULTS: The interrater reliability of the German version of the BI was excellent (mean kappa 0.93). The mean kappa coefficient was 0.79 for the postal version of the BI and 0.80 for the telephone version. Thus, the agreement between the postal and the telephone administration of the BI compared to the face-to-face interview was substantial to excellent. CONCLUSIONS: Our study published the first German version of the BI which was investigated for interrater reliability in a standardized way. The development of a postal and a telephone version allows the widespread use of the German BI for the follow up of stroke patients in different access paths.


Assuntos
Testes Neuropsicológicos , Acidente Vascular Cerebral/diagnóstico , Doença Aguda , Idoso , Feminino , Alemanha , Humanos , Idioma , Masculino , Variações Dependentes do Observador , Reprodutibilidade dos Testes , Acidente Vascular Cerebral/psicologia , Telefone , Resultado do Tratamento
8.
Cephalalgia ; 24(10): 838-43, 2004 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-15377314

RESUMO

Botulinum toxin A has been suggested to be effective in the prophylactic treatment of migraine. However, only very few randomized, double-blind, placebo-controlled studies are available. We designed such a study with a specific focus on different injection sites. Sixty patients with a migraine according to the criteria of the International Headache Society were randomly assigned to receive either placebo in the frontal and neck muscles, or to receive 16 U botulinum toxin A in the frontal muscles and placebo in the neck muscles, or to receive in total 100 U botulinum toxin A in the frontal and neck muscles. The observation period was 3 months. In both treatment groups, 30% of patients showed a reduction of migraine frequency in month 3 by at least 50% compared with baseline, in the placebo group 25% of the patients showed such a reduction (P = 0.921). There were no significant differences between the three study groups with respect to reduction of migraine frequency, number of days with migraine, and the number of total single doses to treat a migraine attack. In the post hoc analysis, the reduction of all accompanying symptoms was significantly higher in the 16 U treatment group compared with the placebo group. In the 100 U treatment group significantly more adverse events occurred compared with the placebo group. All adverse events were mild and transient. Our study did not show any efficacy of botulinum toxin A in the prophylactic treatment of migraine. Only accompanying symptoms were significantly reduced in the 16 U but not in the 100 U treatment group. Future studies should focus on the efficacy of botulinum toxin A in specific subgroups of patients, on the efficacy of repetitive injections, and on other injection sites.


Assuntos
Toxinas Botulínicas Tipo A/administração & dosagem , Transtornos de Enxaqueca/tratamento farmacológico , Adulto , Toxinas Botulínicas Tipo A/uso terapêutico , Método Duplo-Cego , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Transtornos de Enxaqueca/fisiopatologia , Estatísticas não Paramétricas
9.
Cephalalgia ; 23(1): 20-3, 2003 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-12534575

RESUMO

We report the first four German cases of hypnic headache according to the criteria suggested in the literature. Furthermore, we present the results of polysomnography in two theses cases with hypnic headache occurring during REM sleep. In one case, hypnic headache was also associated with periodic limb movements. Although mean nocturnal oxygen saturation was decreased in another patient, nightly oxygen inhalation did not result in an improvement of the headache.


Assuntos
Transtornos da Cefaleia/diagnóstico , Polissonografia , Idoso , Feminino , Transtornos da Cefaleia/etiologia , Transtornos da Cefaleia/fisiopatologia , Humanos , Masculino , Pessoa de Meia-Idade , Oxigênio/sangue , Fatores de Risco , Sono REM/fisiologia
10.
Cephalalgia ; 22(9): 699-710, 2002 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-12421155

RESUMO

The aim of this review is to evaluate the studies available from reference systems and published congress contributions on the prophylactic treatment of idiopathic and cervicogenic headache with botulinum toxin A, and to classify these studies according to evidence-based medicine (EBM) criteria. The studies were analysed with respect to the study design, the number of patients enrolled, the efficacy parameters, and the significance of results. We used the following classification of EBM. I: randomized, controlled study with sufficient number of patients; II: well-designed, controlled study (or randomized, controlled study with insufficient number of patients, no exact diagnosis, missing data of botulinum toxin A dose); III: well-designed, descriptive study; IV: case reports, opinions of experts. For tension-type headache, two studies were found with negative evidence of I with respect to the primary endpoint. There are about as many positive as negative studies with evidence of II or III. For the therapy of migraine, one study with both negative and positive evidence of I, one in part positive study of II, and three positive studies classified as III are available. Two studies on cervicogenic headache with evidence of II and III are contradictory. In addition, we found several positive case reports. For patients with cluster headache, there are positive and negative case reports. We found one positive case report for the treatment of chronic paroxysmal hemicrania. As a result of this analysis, we consider no sufficient positive evidence for a general treatment of idiopathic and cervicogenic headaches with botulinum toxin A to date. Further studies are needed for a definite evaluation of subgroups with benefit from such treatment.


Assuntos
Toxinas Botulínicas Tipo A/uso terapêutico , Medicina Baseada em Evidências , Cefaleia/tratamento farmacológico , Animais , Medicina Baseada em Evidências/métodos , Cefaleia/fisiopatologia , Humanos
11.
Eur J Cell Biol ; 19(3): 216-21, 1979 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-226369

RESUMO

Mouse splenic macrophages were fused with cells of the mouse myeloma line P3-X63-Ag8 in the presence of inactivated Sendai virus. Two continuously growing hybrid cell lines were established from fusion mixtures. These hybrid cell lines exhibited macrophage-like morphology and continued to express macrophage derived Fc receptor activity even after prolonged culture in vitro.


Assuntos
Células Híbridas/imunologia , Fragmentos Fc das Imunoglobulinas , Macrófagos/imunologia , Receptores Imunológicos/metabolismo , Animais , Linhagem Celular , Camundongos , Mieloma Múltiplo , Vírus da Parainfluenza 1 Humana , Baço
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