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1.
Transfus Apher Sci ; 63(2): 103871, 2024 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-38245405

RESUMEN

The histo-blood group antigens P, P1 and Pk are a closely related set of glycosphingolipid structures expressed by red blood cells and other tissues. None of these three characters is expressed on p cells, a null phenotype that arises in the context of homozygous mutation of the A4GALT gene. Subjects with p phenotype spontaneously develop a natural alloantibody named anti-PP1Pk, which is a mixture of IgG and IgM against P1, P and Pk. While anti-P1 is a weak cold antibody with poor clinical significance, anti-P and anti-Pk antibodies are potent haemolysins responsible for severe hemolytic transfusion reactions. The rare anti-PP1Pk alloantibodies are associated with recurrent spontaneous abortion in the first trimester of gestation. P and Pk antigens are expressed at high levels on the placenta and antibodies directed against both these structures are deleterious to placental trophoblasts. Here we describe the use of plasma exchange (PEX) in a nulliparous 39-year-old woman with anti-PP1Pk antibodies and a history of repeated spontaneous early abortions and hypofertility. The patient underwent apheresis starting from the third week throughout the pregnancy and a healthy child was delivered by cesarean section at 35 WG. The newborn required only phototherapy within a few days of life. We can state that an early treatment with the only PEX has proven to be effective and safe in the management of a fetomaternal P-incompatibility caused by a high anti-PP1Pk titer (256).


Asunto(s)
Aborto Habitual , Anemia Hemolítica Autoinmune , Antígenos de Grupos Sanguíneos , Adulto , Femenino , Humanos , Recién Nacido , Embarazo , Aborto Habitual/etiología , Aborto Habitual/terapia , Anemia Hemolítica Autoinmune/terapia , Cesárea/efectos adversos , Isoanticuerpos , Sistema del Grupo Sanguíneo P/genética , Placenta , Intercambio Plasmático/efectos adversos , Mujeres Embarazadas
2.
Euro Surveill ; 24(11)2019 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-30892181

RESUMEN

BACKGROUND: Lyme borreliosis (LB) is the most frequent vector-borne disease in France. Since 2009, surveillance of LB is conducted by a sentinel network of general practitioners (GPs). This system, in conjunction with the national hospitalisation database was used to estimate the incidence and describe the characteristics of LB in France. AIM: To describe the estimated incidence and trends in GP consultations and hospital admissions for LB in France and identify risk groups and high-incidence regions. RESULTS: From 2011 to 2016, the mean yearly incidence rate of LB cases was 53 per 100,000 inhabitants (95% CI: 41-65) ranging from 41 in 2011 to 84 per 100 000 in 2016. A mean of 799 cases per year were hospitalised with LB associated diagnoses 2005-16. The hospitalisation incidence rate (HIR) ranged from 1.1 cases per 100,000 inhabitants in 2005 to 1.5 in 2011 with no statistically significant trend. We observed seasonality with a peak during the summer, important inter-regional variations and a bimodal age distribution in LB incidence and HIR with higher incidence between 5 and 9 year olds and those aged 60 years. Erythema migrans affected 633/667 (95%) of the patients at primary care level. Among hospitalised cases, the most common manifestation was neuroborreliosis 4,906/9,594 (51%). CONCLUSION: Public health strategies should focus on high-incidence age groups and regions during the months with the highest incidences and should emphasise prevention measures such as regular tick checks after exposure and prompt removal to avoid infection.


Asunto(s)
Borrelia burgdorferi/aislamiento & purificación , Enfermedad de Lyme/epidemiología , Admisión del Paciente/estadística & datos numéricos , Alta del Paciente/estadística & datos numéricos , Derivación y Consulta/estadística & datos numéricos , Vigilancia de Guardia , Adolescente , Adulto , Distribución por Edad , Anciano , Anciano de 80 o más Años , Animales , Niño , Preescolar , Bases de Datos Factuales , Femenino , Francia/epidemiología , Médicos Generales , Humanos , Incidencia , Enfermedad de Lyme/diagnóstico , Enfermedad de Lyme/microbiología , Masculino , Persona de Mediana Edad , Admisión del Paciente/tendencias , Derivación y Consulta/tendencias , Estaciones del Año , Enfermedades por Picaduras de Garrapatas/epidemiología , Enfermedades por Picaduras de Garrapatas/microbiología , Adulto Joven
3.
J Appl Microbiol ; 124(1): 188-196, 2018 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-29080227

RESUMEN

AIMS: To evaluate the levels of unicellular and filamentous fungi in ice cubes produced at different levels and to determine their survival in alcoholic beverages and soft drinks. METHODS AND RESULTS: Sixty samples of ice cubes collected from home level (HL) productions, bars and pubs (BP) and industrial manufacturing plants (MP) were investigated for the presence and cell density of yeasts and moulds. Moulds were detected in almost all samples, while yeasts developed from the majority of HL and MP samples. Representative colonies of microfungi were subjected to phenotypic and genotypic characterization. The identification was carried out by restriction fragment length polymorphism (RFLP) analysis of the region spanning the internal transcribed spacers (ITS1 and ITS2) and the 5·8S rRNA gene. The process of yeast identification was concluded by sequencing the D1/D2 region of the 26S rRNA gene. The fungal biodiversity associated with food ice was represented by nine yeast and nine mould species. Strains belonging to Candida parapsilosis and Cryptococcus curvatus, both opportunistic human pathogens, and Penicillium glabrum, an ubiquitous mould in the ice samples analysed, were selected to evaluate the effectiveness of the ice cubes to transfer pathogenic microfungi to consumers, after addition to alcoholic beverages and soft drinks. All strains retained their viability. CONCLUSIONS: The survival test indicated that the most common mode of consumption of ice cubes, through its direct addition to drinks and beverages, did not reduce the viability of microfungi. SIGNIFICANCE AND IMPACT OF THE STUDY: This study evidenced the presence of microfungi in food ice and ascertained their survival in soft drinks and alcoholic beverages.


Asunto(s)
Bebidas/microbiología , Contaminación de Alimentos/análisis , Hongos/crecimiento & desarrollo , Hielo/análisis , Levaduras/crecimiento & desarrollo , ADN de Hongos/genética , Hongos/genética , Hongos/aislamiento & purificación , Viabilidad Microbiana , Levaduras/genética , Levaduras/aislamiento & purificación
4.
Br J Dermatol ; 177(4): 1127-1130, 2017 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-28477365

RESUMEN

Acrodermatitis chronica atrophicans (ACA) is the late cutaneous form of Lyme borreliosis. The early inflammatory phase manifests with a bluish-red discoloration and doughy swelling of the skin. The atrophic phase represents a late-phase process with red discoloration, and a thin and wrinkled appearance of the skin. We present a patient who exhibited a previously undescribed form of late cutaneous Lyme borreliosis (LCLB) with a foot tumour. A 64-year-old woman had a large tumorous lesion on the right sole. The tumour size and deformation of the feet made wearing shoes difficult. On skin histology, a granulomatous lymphohistiocytic infiltrate with plasma cells was noticed. In fact, the patient recalled tick bites 2 or 3 years before. Borrelia burgdorferi (Bb) serology was highly positive and a polymerase chain reaction analysis on the skin biopsy detected Bb sensu lato, genospecies B. afzelii. We diagnosed LCLB and antibiotics were prescribed. On the more recent examination, the tumour had totally disappeared; the skin was atrophic and dry with only few scales. We report an atypical case of European LCLB, suggesting that ACA is not the only possible presentation of LCLB. The diagnosis of ACA is often clinically missed for months or years, and may be mistaken at the inflammation phase for vascular disorders, erysipelas or bursitis/arthritis, and at the atrophic phase for lichen sclerosus atrophicus, morphoea or anetoderma. To our knowledge, no such tumorous LCLB has previously been described.


Asunto(s)
Enfermedades del Pie/diagnóstico , Enfermedad de Lyme/diagnóstico , Enfermedades Cutáneas Bacterianas/diagnóstico , Acrodermatitis/diagnóstico , Acrodermatitis/tratamiento farmacológico , Antibacterianos/uso terapéutico , Grupo Borrelia Burgdorferi , Diagnóstico Diferencial , Femenino , Enfermedades del Pie/tratamiento farmacológico , Humanos , Enfermedad de Lyme/tratamiento farmacológico , Persona de Mediana Edad , Enfermedades Cutáneas Bacterianas/tratamiento farmacológico , Mordeduras de Garrapatas
5.
Clin Epigenetics ; 15(1): 53, 2023 03 29.
Artículo en Inglés | MEDLINE | ID: mdl-36991505

RESUMEN

BACKGROUND: The present study investigates whether epigenetic differences emerge in the heart of patients undergoing cardiac surgery for an aortic valvular replacement (AVR) or coronary artery bypass graft (CABG). An algorithm is also established to determine how the pathophysiological condition might influence the human biological cardiac age. RESULTS: Blood samples and cardiac auricles were collected from patients who underwent cardiac procedures: 94 AVR and 289 CABG. The CpGs from three independent blood-derived biological clocks were selected to design a new blood- and the first cardiac-specific clocks. Specifically, 31 CpGs from six age-related genes, ELOVL2, EDARADD, ITGA2B, ASPA, PDE4C, and FHL2, were used to construct the tissue-tailored clocks. The best-fitting variables were combined to define new cardiac- and blood-tailored clocks validated through neural network analysis and elastic regression. In addition, telomere length (TL) was measured by qPCR. These new methods revealed a similarity between chronological and biological age in the blood and heart; the average TL was significantly higher in the heart than in the blood. In addition, the cardiac clock discriminated well between AVR and CABG and was sensitive to cardiovascular risk factors such as obesity and smoking. Moreover, the cardiac-specific clock identified an AVR patient's subgroup whose accelerated bioage correlated with the altered ventricular parameters, including left ventricular diastolic and systolic volume. CONCLUSION: This study reports on applying a method to evaluate the cardiac biological age revealing epigenetic features that separate subgroups of AVR and CABG.


Asunto(s)
Metilación de ADN , Implantación de Prótesis de Válvulas Cardíacas , Humanos , Implantación de Prótesis de Válvulas Cardíacas/efectos adversos , Implantación de Prótesis de Válvulas Cardíacas/métodos , Resultado del Tratamiento , Válvula Aórtica/cirugía , Epigénesis Genética
6.
Encephale ; 38(6): 488-95, 2012 Dec.
Artículo en Francés | MEDLINE | ID: mdl-23200615

RESUMEN

OBJECTIVE: This study investigated the cognitive skills in pervasive developmental disorders (PDD). METHODOLOGY: Two groups of children participated in this study, 39 individuals with autism and 18 individuals with Asperger syndrome. Each participant was assessed by the Wechsler scales: WPPSI-III, WISC-III or WISC-IV. RESULTS: Children with Asperger syndrome have VIQ more than PIQ and the children with autism have VIQ less than PIQ. The performances in "block design" task vary according to the cognitive level and not according to the PDD type. The high-functioning autistic children show high performance in "block design" task. Children with Asperger syndrome revealed impairments in the "understanding of social situations" task. DISCUSSION: Individuals with autism have a verbal intelligence quotient lower than individuals with an Asperger syndrome. Several hypotheses have tried to explain verbal differences between children with autism and Asperger syndrome. A first hypothesis proposed a developmental convergence between these two groups. A second hypothesis suggested that communication and social interaction impairments could be implicated in verbal skills. A third hypothesis supported that individuals with Asperger syndrome could develop a specific cognitive style. Children with autism have spatial and perceptive capacities better than verbal capacities. These performances could be interpreted as the expression of a specific cognitive style based on the visual analysis of the detail. CONCLUSION: The low-functioning children with autism have a cognitive profile with PIQ more than VIQ and high skills in spatial organization. The high-level children with autism have a cognitive profile with PIQ more than VIQ and high skills in spatial abstraction. Children with Asperger syndrome have a profile VIQ more than PIQ profile, they are particularly good in verbal learning notably vocabulary.


Asunto(s)
Síndrome de Asperger/diagnóstico , Trastornos Generalizados del Desarrollo Infantil/diagnóstico , Trastornos del Conocimiento/diagnóstico , Escalas de Wechsler/estadística & datos numéricos , Síndrome de Asperger/psicología , Niño , Trastornos Generalizados del Desarrollo Infantil/psicología , Trastornos del Conocimiento/psicología , Diagnóstico Diferencial , Femenino , Francia , Humanos , Discapacidad Intelectual/diagnóstico , Discapacidad Intelectual/psicología , Inteligencia , Trastornos del Desarrollo del Lenguaje/diagnóstico , Trastornos del Desarrollo del Lenguaje/psicología , Masculino , Psicometría/estadística & datos numéricos , Reproducibilidad de los Resultados , Teoría de la Mente , Aprendizaje Verbal , Vocabulario
7.
Infect Dis Now ; 51(7): 627-629, 2021 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-33870892

RESUMEN

Borreliosis is a common affliction in northern countries and its neurological manifestations often mislead trained clinicians. We present three cases of Lyme neuroborreliosis, with intrathecal synthesis of specific antibodies, lymphocytic meningitis and magnetic-resonance imaging (MRI) findings. Our description aims at illustrating the natural history of the infection, highlighting persistent intrathecal synthesis of anti-Borrelia antibodies months after treatment completion, and its clinical significance. We then review the literature on MRI findings in neuroborreliosis and the kinetics of intrathecal synthesis of specific anti-Borrelia antibodies.


Asunto(s)
Borrelia , Neuroborreliosis de Lyme , Anticuerpos Antibacterianos , Humanos , Inmunoglobulina G , Cinética , Neuroborreliosis de Lyme/diagnóstico
8.
J Clin Microbiol ; 48(5): 1758-66, 2010 May.
Artículo en Inglés | MEDLINE | ID: mdl-20220173

RESUMEN

The aim of the present study was to investigate the use of the SNaPshot minisequencing method for the identification of Mycobacterium tuberculosis complex (MTBC) isolates to the species level and for further genotyping of M. tuberculosis isolates. We developed an innovative strategy based on two multiplex allele-specific minisequencing assays that allowed detection of eight species-specific and eight lineage-specific single nucleotide polymorphisms (SNPs). Each assay consisted of an eightplex PCR amplification, followed by an eightplex minisequencing reaction with the SNaPshot multiplex kit (Applied Biosystems) and, finally, analysis of the extension products by capillary electrophoresis. The whole strategy was developed with a panel of 56 MTBC strains and 15 negative controls. All MTBC strains tested except one M. africanum clinical isolate were accurately identified to the species level, and all M. tuberculosis isolates were successfully further genotyped. This two-step strategy based on SNaPshot minisequencing allows the simultaneous differentiation of closely related members of the MTBC, the distinction between principal genetic groups, and the characterization of M. tuberculosis isolates into one of the seven prominent SNP cluster groups (SCGs) and could be a useful tool for diagnostic and epidemiological purposes.


Asunto(s)
Técnicas Bacteriológicas/métodos , Mycobacterium tuberculosis/clasificación , Mycobacterium tuberculosis/aislamiento & purificación , Análisis de Secuencia de ADN/métodos , Técnicas de Tipificación Bacteriana , Cartilla de ADN/genética , Electroforesis Capilar/métodos , Genotipo , Humanos , Epidemiología Molecular/métodos , Mycobacterium tuberculosis/genética , Reacción en Cadena de la Polimerasa/métodos , Polimorfismo de Nucleótido Simple
9.
AJNR Am J Neuroradiol ; 41(10): 1916-1922, 2020 10.
Artículo en Inglés | MEDLINE | ID: mdl-32819908

RESUMEN

BACKGROUND AND PURPOSE: The association of arterial tortuosity and connective tissue diseases is widely reported in the literature, but only a few studies were based on a quantitative evaluation of this arterial phenotype, and none of the latter examined the intracranial vasculature. The aim of this study was to evaluate the degree of intracranial arterial tortuosity in patients with Marfan syndrome and those with Loeys-Dietz syndrome, and to assess its usefulness in the differential diagnosis. MATERIALS AND METHODS: We performed a retrospective analysis of 68 patients with genetically confirmed Marfan syndrome (n = 36) or Loeys-Dietz syndrome (n = 32), who underwent at least 1 MRA of the brain at our institution. Fifty-two controls were randomly selected among patients who presented with headache and without any known comorbidity. Tortuosity indexes of 4 intracranial arterial segments were measured on a 3D volume-rendered angiogram by using the following formula: [Formula: see text]. RESULTS: Both Marfan syndrome and Loeys-Dietz syndrome showed a significantly higher tortuosity index compared with controls in all examined vessels. The tortuosity index of the vertebrobasilar system showed an excellent interrater reliability (intraclass correlation coefficient, 0.99) and was the strongest independent predictor of Loeys-Dietz syndrome in patients with connective tissue disease (P = .002), with a 97% specificity for this pathology when its value was > 60. CONCLUSIONS: The tortuosity index of intracranial arteries is an easily calculated and highly reproducible measure, which shows a high specificity for Marfan syndrome and Loeys-Dietz syndrome and may be useful in differentiating these 2 entities.


Asunto(s)
Arterias/patología , Encéfalo/patología , Síndrome de Loeys-Dietz/diagnóstico por imagen , Síndrome de Loeys-Dietz/patología , Síndrome de Marfan/diagnóstico por imagen , Síndrome de Marfan/patología , Adulto , Arterias/diagnóstico por imagen , Encéfalo/diagnóstico por imagen , Angiografía Cerebral/métodos , Diagnóstico Diferencial , Femenino , Humanos , Interpretación de Imagen Asistida por Computador/métodos , Angiografía por Resonancia Magnética/métodos , Masculino , Persona de Mediana Edad , Reproducibilidad de los Resultados , Estudios Retrospectivos , Adulto Joven
10.
Br J Dermatol ; 161(1): 174-6, 2009 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-19302068

RESUMEN

BACKGROUND: Only about 30 cases of borrelial lymphocytoma (BL) with identification of the causative species of Borrelia have been published to date, mainly from Eastern or Central European countries. OBJECTIVES: To identify the species of B. burgdorferi complex responsible for BL in France. METHODS: Nine patients with BL acquired in France and for whom skin samples were sent to the national reference centre laboratory between 1994 and 2007 were included in this retrospective study. Direct detection of Borrelia in skin samples was made by polymerase chain reaction targeting the fla gene. Culture was performed when technically possible, and identification of each species was made by hybridization of a fragment of the fla gene with a panel of species-specific oligonucleotides. RESULTS: Borrelia afzelii was identified in three cases, B. garinii and B. burgdorferi sensu stricto in one case each. Culture was positive in only one case (B. garinii). CONCLUSIONS: Borrelia afzelii seems to be the predominant species of Borrelia responsible for BL in France, as already reported in other European countries.


Asunto(s)
Grupo Borrelia Burgdorferi/aislamiento & purificación , Enfermedad de Lyme/microbiología , Seudolinfoma/microbiología , Adulto , Anciano , Anciano de 80 o más Años , Biopsia , Grupo Borrelia Burgdorferi/clasificación , Grupo Borrelia Burgdorferi/genética , Niño , ADN Bacteriano/análisis , Femenino , Flagelina/genética , Francia , Humanos , Masculino , Persona de Mediana Edad , Reacción en Cadena de la Polimerasa , Estudios Retrospectivos
11.
Rev Neurol (Paris) ; 163(11): 1039-47, 2007 Nov.
Artículo en Francés | MEDLINE | ID: mdl-18033042

RESUMEN

INTRODUCTION: Acute myelitis accounts for 4 to 5 percent of all cases of neuroborreliosis. In the literature, simultaneous spinal MRI and cerebrospinal fluid (CSF) investigations are presented for only 8 cases. We describe here 3 cases of acute Lyme myelitis. METHOD: In a cohort of 45 patients with neuroborreliosis, diagnosed between January 1998 and January 2005, 3 had acute myelitis. Clinical, biological and radiological data were studied. CASE REPORTS: The three patients had motor, sensorial and sphincter involvement. Extra-spinal involvement, such as fever and headache for one, facial nerve palsy for the second and subarachnoid hemorrhage for the third, was also noted. Pleocytosis varied from 10 to 520 white cells per mm3. Lyme serology was positive in CSF for all. Intrathecal anti-Borrelia antibody index was positive or intermediate for all three patients. Spinal cord MRI revealed a large hyperintense zone involving more than 3 vertebral segments. Myelitis was central, posterior or transverse in the axial plane. The clinical course was favorable after a three-week course of appropriate antibiotics. CONCLUSION: These 3 cases and the others from the literature show the diversity of the clinical and radiological features of acute myelitis: transverse, central or posterior myelitis. Thus, Lyme serology in CSF in indicated for patients presenting acute myelitis, particularly in endemic areas.


Asunto(s)
Enfermedad de Lyme/complicaciones , Mielitis/etiología , Enfermedad Aguda , Anciano , Antibacterianos/uso terapéutico , Anticuerpos Antibacterianos/análisis , Anticuerpos Antibacterianos/líquido cefalorraquídeo , Western Blotting , Borrelia burgdorferi/inmunología , Estudios de Cohortes , Ensayo de Inmunoadsorción Enzimática , Femenino , Humanos , Leucocitosis/etiología , Enfermedad de Lyme/tratamiento farmacológico , Enfermedad de Lyme/patología , Imagen por Resonancia Magnética , Masculino , Persona de Mediana Edad , Mielitis/tratamiento farmacológico , Mielitis/patología , Mielitis Transversa/tratamiento farmacológico , Mielitis Transversa/etiología , Mielitis Transversa/patología , Médula Espinal/patología
12.
Arch Pediatr ; 14(3): 234-8, 2007 Mar.
Artículo en Francés | MEDLINE | ID: mdl-17208423

RESUMEN

OBJECTIVE: To determine developmental communication profiles in young autistic children with mental retardation. METHODS: A group of 19 autistic children (mean age=43 months) were matched with a group of 11 mentally retarded children (mean age=39 months) on mental age (17,6 months). All of these children were without speech (less than 5 words of vocabulary). Communication skills were assessed with the Guidetti-Tourrette scales (ECSP), French adaptation of the Seibert-Hogan scales. RESULTS: Autistic children displayed a much lower score than mentally retarded children in the 3 functions of early social communication (behavior regulation, social interaction and joint attention). The developmental communication profiles was the same in the 2 groups. DISCUSSION: The results showed evidence of distortion in autistic children development: they displayed important deficits in communication skills, in comparison with cognitive skills. Autistic children mainly displayed requesting gestures: they used adults to help them to reach a goal, instead of regarding them as social partners. However, young children who have mental age less than 18 months mainly use the same functions of communication, with or without autistic trouble. CONCLUSIONS: There is a same developmental sequence in communication skills in young children, with or without autistic trouble.


Asunto(s)
Trastorno Autístico/psicología , Comunicación , Discapacidad Intelectual/psicología , Preescolar , Humanos
13.
Med Mal Infect ; 37(7-8): 496-506, 2007.
Artículo en Francés | MEDLINE | ID: mdl-17512148

RESUMEN

The biological diagnosis of Borrelia burgdorferi sensu lato infection is usually made by antibody detection in patient sera. Thus, serological testing (Elisa, immunoblotting) is essential for a biological diagnosis. Specific antibody detection is usually done in serum and CSF of patients suspected of Lyme borreliosis. Laboratories must follow European recommendations to validate these assays in routine practice. Antibody detection lacks sensitivity in the early cutaneous phase of the infection. Therefore, serological testing is not recommended for the diagnosis of erythema migrans. The interpretation of serology must take into account the variability of Elisa sensitivity and specificity and the lack of standardization for Western-blotting in Europe. Besides these indirect diagnosis techniques, there is also direct detection of spirochetes by culture or by in vitro DNA amplification but these require adequate samples. These molecular tests must not be performed routinely, but only for specific clinical situations and in specialized laboratories only.


Asunto(s)
Enfermedad de Lyme/diagnóstico , Antígenos de Superficie/análisis , Antígenos de Superficie/genética , Artritis/microbiología , Proteínas de la Membrana Bacteriana Externa/análisis , Proteínas de la Membrana Bacteriana Externa/genética , Vacunas Bacterianas/análisis , Vacunas Bacterianas/genética , Grupo Borrelia Burgdorferi/genética , Grupo Borrelia Burgdorferi/crecimiento & desarrollo , Grupo Borrelia Burgdorferi/aislamiento & purificación , Humanos , Técnicas para Inmunoenzimas , Pruebas Inmunológicas/métodos , Lipoproteínas/análisis , Lipoproteínas/genética , Enfermedad de Lyme/inmunología , Neuroborreliosis de Lyme , Examen Físico
14.
J Fr Ophtalmol ; 40(8): 654-660, 2017 Oct.
Artículo en Francés | MEDLINE | ID: mdl-28867237

RESUMEN

OBJECTIVE: After a decade of constant decline, the number of syphilis cases has been steadily increasing since the 2000s, particularly in HIV infected patients. Neurosyphilis is a rare manifestation of this sexually transmitted disease for which we performed a retrospective study and analyzed clinical manifestations. PATIENTS AND METHODS: We reviewed retrospectively all the neurosyphilis cases admitted to Strasbourg University Hospital between 2004 and 2014. We included and analyzed 13 patients admitted during this period who met the diagnostic criteria for neurosyphilis. RESULTS: Nine of 13 patients had isolated visual manifestations; three (23.1%) experienced posterior uveitis, two (15.4%), panuveitis, and 4 (30.8%) had papillitis. Out of five patients (38.5%) who were HIV positive, three (60%) had a CD4 cell count above 400/mm3 at the time of diagnosis of neurosyphilis. All patients received parenteral penicillin G or cephalosporin, and 5/13 (38.5%) received systemic corticotherapy. CONCLUSION: Ophthalmologists appear as key players in the identification, management and follow-up of neurosyphilis, since ocular findings are key diagnostic features in these patients.


Asunto(s)
Infecciones Bacterianas del Ojo/diagnóstico , Neurosífilis/diagnóstico , Adulto , Anciano de 80 o más Años , Diagnóstico Diferencial , Infecciones Bacterianas del Ojo/etiología , Femenino , Francia , Infecciones por VIH/complicaciones , Infecciones por VIH/diagnóstico , VIH-1 , Hospitales Universitarios , Humanos , Masculino , Persona de Mediana Edad , Neurosífilis/etiología , Estudios Retrospectivos
15.
Clin Microbiol Infect ; 12(6): 576-9, 2006 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-16700708

RESUMEN

The automated MagNA Pure DNA extraction method for Chlamydia trachomatis was compared with the manual Cobas Amplicor protocol using 100 microL of input sample volume from 964 specimens. Agreement between protocols was 96.1%. The automated extraction method had a sensitivity of 99% and a specificity of 100%. Amplification inhibition observed after manual preparation of samples (3.8%) was not apparent following automated extraction. Using 200 microL of sample in the automated extraction process lowered the detection limit without raising the inhibition rate. Furthermore, the automated extraction method halved the hands-on time required for the procedure.


Asunto(s)
Infecciones por Chlamydia/diagnóstico , Chlamydia trachomatis/aislamiento & purificación , ADN Bacteriano/aislamiento & purificación , Técnicas de Amplificación de Ácido Nucleico/normas , Juego de Reactivos para Diagnóstico/normas , Automatización , Infecciones por Chlamydia/microbiología , Chlamydia trachomatis/genética , ADN Bacteriano/análisis , Femenino , Humanos , Masculino , Reproducibilidad de los Resultados , Sensibilidad y Especificidad , Sistema Urogenital/microbiología
16.
Phys Rev E Stat Nonlin Soft Matter Phys ; 72(4 Pt 2): 046712, 2005 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-16383572

RESUMEN

A not trivial problem for every experimental time series associated to a natural system is to individuate the significant variables to describe the dynamics, i.e., the effective degrees of freedom. The application of independent component analysis (ICA) has provided interesting results in this direction, e.g., in the seismological and atmospheric field. Since all natural phenomena can be represented by dynamical systems, our aim is to check the performance of ICA in this general context to avoid ambiguities when investigating an unknown experimental system. We show many examples, representing linear, nonlinear, and stochastic processes, in which ICA seems to be an efficacious preanalysis able to give information about the complexity of the dynamics.

17.
Clin Infect Dis ; 37(6): 846-8, 2003 Sep 15.
Artículo en Inglés | MEDLINE | ID: mdl-12955649

RESUMEN

Human anaplasmosis is a febrile illness caused by Anaplasma phagocytophilum, an intracellular bacterium transmitted by Ixodes ticks in the United States and Europe. Although cough is reported in 30% of the American cases, interstitial pneumonitis has been noted only once. Of the 9 confirmed cases reported in Europe, 3 presented with atypical pneumonitis. A. phagocytophilum should be added to the list of agents responsible for interstitial pneumonitis, especially in areas where human anaplasmosis is endemic.


Asunto(s)
Anaplasma phagocytophilum , Anaplasmosis/fisiopatología , Neumonía/etiología , Enfermedades por Picaduras de Garrapatas/fisiopatología , Anaplasmosis/diagnóstico por imagen , Anaplasmosis/epidemiología , Francia/epidemiología , Humanos , Masculino , Persona de Mediana Edad , Datos de Secuencia Molecular , Radiografía , Enfermedades por Picaduras de Garrapatas/epidemiología
18.
Eur J Clin Nutr ; 54(2): 155-8, 2000 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-10694787

RESUMEN

OBJECTIVE: The aim of this study was to evaluate the effects of an oligoantigenic and histamine-free diet on patients affected with chronic idiopathic urticaria (CIU). DESIGN: Ten patients with chronic idiopathic urticaria were prescribed an oligoantigenic and histamine-free diet for 21 days, followed by serial and controlled reintroduction of foods during a further 70 days. Modification in clinical illness as well as histamine plasma levels, post-heparin plasma diamine oxidase (DAO) and intestinal permeability were evaluated. RESULTS: The oligoantigenic and histamine-free diet induced a significant improvement of symptoms (P<0.05). Moreover, CIU patients on free diet showed higher histamine plasma levels (P<0. 05 vs post-diet and vs controls) that fell to control levels during the oligoantigenic and histamine-free diet. Post-heparin plasma diamine oxidase values were slightly reduced and were unchanged during the diet as well as intestinal permeability, which was always normal in all patients. CONCLUSIONS: These data suggest that histamine plays a major role in chronic idiopathic urticaria. The finding of normal intestinal permeability suggests that a morphological damage of intestinal mucosa should be excluded in these patients. However, the presence of low levels of post-heparin plasma diamine oxidase may indicate a subclinical impairment of small bowel enterocyte function that could induce a higher sensitivity to histamine-rich or histamine-producing food. European Journal of Clinical Nutrition (2000) 54, 155-158


Asunto(s)
Dieta , Histamina/administración & dosificación , Histamina/sangre , Urticaria/dietoterapia , Adulto , Amina Oxidasa (conteniendo Cobre)/sangre , Antígenos/administración & dosificación , Enfermedad Crónica , Femenino , Hipersensibilidad a los Alimentos/inmunología , Humanos , Absorción Intestinal , Masculino , Persona de Mediana Edad , Inducción de Remisión
19.
Phys Rev E Stat Nonlin Soft Matter Phys ; 70(6 Pt 2): 067301, 2004 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-15697560

RESUMEN

Based on the generalized kinetic equation for the one-particle distribution function with a small source, the transition from the kinetic to the hydrodynamic description of many-particle systems is performed. The basic feature of this interesting technique to obtain the hydrodynamic limit is that the latter has been partially incorporated into the kinetic equation itself. The hydrodynamic equations for capillary fluids are derived from the characteristic function for the local moments of the distribution function. Fick's law appears as a consequence of the transformation law for the hydrodynamic quantities under time inversion.

20.
Phys Rev E Stat Nonlin Soft Matter Phys ; 63(1 Pt 2): 016501, 2001 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-11304370

RESUMEN

We introduce a description of the collective transverse dynamics of charged (proton) beams in the stability regime by suitable classical stochastic fluctuations. In this scheme, the collective beam dynamics is described by time-reversal invariant diffusion processes deduced by stochastic variational principles (Nelson processes). By general arguments, we show that the diffusion coefficient, expressed in units of length, is given by lambda(c)sqrt[N], where N is the number of particles in the beam and lambda(c) the Compton wavelength of a single constituent. This diffusion coefficient represents an effective unit of beam emittance. The hydrodynamic equations of the stochastic dynamics can be easily recast in the form of a Schrödinger equation, with the unit of emittance replacing the Planck action constant. This fact provides a natural connection to the so-called "quantum-like approaches" to beam dynamics. The transition probabilities associated to Nelson processes can be exploited to model evolutions suitable to control the transverse beam dynamics. In particular we show how to control, in the quadrupole approximation to the beam-field interaction, both the focusing and the transverse oscillations of the beam, either together or independently.

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