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1.
HIV Med ; 19(2): 102-117, 2018 02.
Artigo em Inglês | MEDLINE | ID: mdl-28984429

RESUMO

OBJECTIVES: There are currently few data on the long-term risk of cancer and death in individuals taking raltegravir (RAL). The aim of this analysis was to evaluate whether there is evidence for an association. METHODS: The EuroSIDA cohort was divided into three groups: those starting RAL-based combination antiretroviral therapy (cART) on or after 21 December 2007 (RAL); a historical cohort (HIST) of individuals adding a new antiretroviral (ARV) drug (not RAL) to their cART between 1 January 2005 and 20 December 2007, and a concurrent cohort (CONC) of individuals adding a new ARV drug (not RAL) to their cART on or after 21 December 2007. Baseline characteristics were compared using logistic regression. The incidences of newly diagnosed malignancies and death were compared using Poisson regression. RESULTS: The RAL cohort included 1470 individuals [with 4058 person-years of follow-up (PYFU)] compared with 3787 (4472 PYFU) and 4467 (10 691 PYFU) in the HIST and CONC cohorts, respectively. The prevalence of non-AIDS-related malignancies prior to baseline tended to be higher in the RAL cohort vs. the HIST cohort [adjusted odds ratio (aOR) 1.31; 95% confidence interval (CI) 0.95-1.80] and vs. the CONC cohort (aOR 1.89; 95% CI 1.37-2.61). In intention-to-treat (ITT) analysis (events: RAL, 50; HIST, 45; CONC, 127), the incidence of all new malignancies was 1.11 (95% CI 0.84-1.46) per 100 PYFU in the RAL cohort vs. 1.20 (95% CI 0.90-1.61) and 0.83 (95% CI 0.70-0.99) in the HIST and CONC cohorts, respectively. After adjustment, there was no evidence for a difference in the risk of malignancies [adjusted rate ratio (RR) 0.73; 95% CI 0.47-1.14 for RALvs. HIST; RR 0.95; 95% CI 0.65-1.39 for RALvs. CONC] or mortality (adjusted RR 0.87; 95% CI 0.53-1.43 for RALvs. HIST; RR 1.14; 95% CI 0.76-1.72 for RALvs. CONC). CONCLUSIONS: We found no evidence for an oncogenic risk or poorer survival associated with using RAL compared with control groups.


Assuntos
Antirretrovirais/administração & dosagem , Terapia Antirretroviral de Alta Atividade/métodos , Infecções por HIV/complicações , Infecções por HIV/tratamento farmacológico , Neoplasias/epidemiologia , Neoplasias/mortalidade , Raltegravir Potássico/administração & dosagem , Adulto , Feminino , Humanos , Incidência , Masculino , Pessoa de Meia-Idade , Estudos Prospectivos , Medição de Risco , Análise de Sobrevida
2.
Euro Surveill ; 16(45)2011 Nov 10.
Artigo em Inglês | MEDLINE | ID: mdl-22114976

RESUMO

An increased number of legionellosis cases in 2011 has been reported in Latvia, compared to the ten previous years. A total of 30 legionellosis cases (1.35 per 100,000 inhabitants), including 19 females, have been confirmed until the end of September 2011. The majority of cases (n=23) were inhabitants of the capital city Riga. The reason for the increase in legionellosis is unclear. Twenty-six of the 30 cases are not travel-related.


Assuntos
Legionelose/epidemiologia , Microbiologia da Água , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Formação de Anticorpos , Antígenos de Bactérias/urina , Notificação de Doenças , Feminino , Humanos , Letônia/epidemiologia , Legionella/imunologia , Legionella/isolamento & purificação , Legionella/patogenicidade , Legionelose/imunologia , Legionelose/microbiologia , Legionelose/transmissão , Masculino , Pessoa de Meia-Idade , Prevalência , Adulto Jovem
3.
Bull Exp Biol Med ; 146(6): 875-7, 2008 Dec.
Artigo em Inglês, Russo | MEDLINE | ID: mdl-19513410

RESUMO

Measurements of nitrogen oxide and copper in the blood of 57 patients with chronic viral hepatitis C was carried out before antiviral therapy by electron paramagnetic resonance on a Radiopan EPR spectrometer. The results indicate elevated levels of nitrogen oxide and copper in the blood of these patients in comparison with normal subjects. Comparison of these findings with the results of a previous analysis of redox status of patients with chronic viral hepatitis C indicate that this disease is characterized by a significant pro-oxidant shift in the realization of redox processes and disorders in the metal ligand homeostasis (at least as regards copper).


Assuntos
Cobre/sangue , Espectroscopia de Ressonância de Spin Eletrônica/métodos , Hepatite C Crônica/sangue , Óxidos de Nitrogênio/sangue , Adolescente , Adulto , Idoso , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Adulto Jovem
4.
Genetika ; 44(10): 1379-84, 2008 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-19062534

RESUMO

Wilson disease (WD) is an autosomal recessive disorder of copper metabolism characterized by hepatic and/or neurological damage. More than 300 mutations in the gene ATP7B causing this defect have been reported. The data on correlation between WD patient genotypes and clinical presentation are controversial. In this paper the results of ATP7B mutation analysis by testing for mutation H1069Q and direct sequencing of six exons together with the clinical data of 40 Latvian WD patients are presented. Two previously described and two novel mutations as well as one previously reported polymorphism were identified. The H1069Q mutation was present at 52.5% of the disease alleles. One individual among 157 healthy Latvians was also found to be a mutation H1069Q carrier. The estimated incidence of WD in Latvia is approximately 1 in 25600. Wide clinical variability was observed among individuals with the same ATP7B genotype, thus supporting the suggestion that modifying factors play an additional role in the pathogenesis of WD. An algorithm for the diagnosis of WD, including testing for mutation H1069Q, is recommended for the populations where mutation H1069Q accounts for 50% of WD alleles or more.


Assuntos
Adenosina Trifosfatases/genética , Alelos , Substituição de Aminoácidos , Proteínas de Transporte de Cátions/genética , Degeneração Hepatolenticular/diagnóstico , Degeneração Hepatolenticular/genética , Mutação de Sentido Incorreto , Adenosina Trifosfatases/metabolismo , Adolescente , Adulto , Algoritmos , Proteínas de Transporte de Cátions/metabolismo , Criança , Cobre/metabolismo , ATPases Transportadoras de Cobre , Análise Mutacional de DNA/métodos , Diagnóstico Diferencial , Éxons/genética , Feminino , Genótipo , Degeneração Hepatolenticular/epidemiologia , Degeneração Hepatolenticular/metabolismo , Humanos , Incidência , Letônia , Masculino , Polimorfismo Genético/genética
5.
J Neurol Neurosurg Psychiatry ; 77(12): 1350-3, 2006 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-16754695

RESUMO

BACKGROUND: In Latvia and other endemic regions, a single tick bite has the potential to transmit both tick-borne encephalitis (TBE) and Lyme borreliosis. OBJECTIVE: To analyse both the clinical features and differential diagnosis of combined tick-borne infection with TBE and Lyme borreliosis, in 51 patients with serological evidence, of whom 69% had tick bites. RESULTS: Biphasic fever suggestive of TBE occurred in 55% of the patients. Meningitis occurred in 92%, with painful radicular symptoms in 39%. Muscle weakness occurred in 41%; in 29% the flaccid paralysis was compatible with TBE. Only two patients presented with the bulbar palsy typical of TBE. Typical Lyme borreliosis facial palsy occurred in three patients. Typical TBE oculomotor disturbances occurred in two. Other features typical of Lyme borreliosis detected in our patients were distal peripheral neuropathy (n = 4), arthralgia (n = 9), local erythema 1-12 days after tick bite (n = 7) and erythema chronicum migrans (n = 1). Echocardiogram abnormalities occurred in 15. CONCLUSIONS: Patients with double infection with TBE and Lyme borreliosis fell into three main clinical groups: febrile illness, 3 (6%); meningitis, 15 (30%); central or peripheral neurological deficit (meningoencephalitis, meningomyelitis, meningoradiculitis and polyradiculoneuritis), 33 (65%). Systemic features pointing to Lyme borreliosis were found in 25 patients (49%); immunoglobulin (Ig)M antibodies to borreliosis were present in 18 of them. The clinical occurrence of both Lyme borreliosis and TBE vary after exposure to tick bite, and the neurological manifestations of each disorder vary widely, with considerable overlap. This observational study provides no evidence that co-infection produces unusual manifestations due to unpredicted interaction between the two diseases. Patients with tick exposure presenting with acute neurological symptoms in areas endemic for both Lyme borreliosis and TBE should be investigated for both conditions. The threshold for simultaneous treatment of both conditions should be low, given the possibility of co-occurrence and the difficulty in ascribing individual neurological manifestations to one condition or the other.


Assuntos
Encefalite Transmitida por Carrapatos/diagnóstico , Encefalite Transmitida por Carrapatos/patologia , Doença de Lyme/diagnóstico , Doença de Lyme/patologia , Mordeduras e Picadas , Diagnóstico Diferencial , Encefalite Transmitida por Carrapatos/complicações , Feminino , Febre/etiologia , Humanos , Letônia , Doença de Lyme/complicações , Masculino , Meningite/etiologia , Pessoa de Meia-Idade , Doenças do Sistema Nervoso/etiologia , Estudos Retrospectivos
6.
J Neurol Neurosurg Psychiatry ; 76(11): 1555-7, 2005 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-16227550

RESUMO

INTRODUCTION AND METHODS: We report 20 patients aged 18-24 years from Latvia with diphtheritic polyneuropathy. All lived in a closed community and 80% were known to have been fully vaccinated against diphtheria until at least 14 years old. Diphtheria antitoxin had been administered within 3 days of the onset of upper respiratory tract infection in 16 patients and 15 received antibiotics. RESULTS: Neurological symptoms developed after a median of 43 days (range 35-58) compared to only 10 days in previous studies of unvaccinated patients. All showed evidence of mild limb polyneuropathy with electrophysiological evidence of polyneuropathy. Only 30% showed early bulbar abnormalities compared to the usual rate of over 95% in diphtheritic polyneuropathy. However, 45% had later bulbar deterioration coinciding with the limb polyneuropathy. CONCLUSIONS: These patients show that an attenuated form of polyneuropathy of later onset, with less prominent early bulbar features, can occur in patients vaccinated against diphtheria according to schedule but living in a closed community in a country where diphtheria remains endemic.


Assuntos
Toxoide Diftérico/administração & dosagem , Difteria/epidemiologia , Difteria/prevenção & controle , Imunização Secundária/estatística & dados numéricos , Polineuropatias/epidemiologia , Adolescente , Adulto , Difteria/fisiopatologia , Humanos , Masculino , Tonsila Palatina/fisiopatologia , Faringe/fisiopatologia , Características de Residência
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