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1.
J Nutr Sci Vitaminol (Tokyo) ; 64(3): 209-214, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-29962432

RESUMO

The association between advanced age and the thiamine concentration has not been conclusively determined. A recent report from Japan showed that more than half of nursing home elderly residents at an institution had a low whole-blood thiamine concentration (<20 ng/mL). Therefore, a high incidence of low thiamine concentrations among hospitalized elderly has been anticipated in the Japanese population but never investigated. We evaluated the whole thiamine concentration in newly hospitalized elderly patients (≥65 y old) with infectious diseases. Evaluations were performed on admission and at days 6-8 of hospitalization with liquid chromatography tandem mass spectrometry (LC/MS/MS). As a result, we enrolled a total of 471 patients from September 2015 to December 2016. The median thiamine concentration was 46 ng/mL (IQR, 37-58 ng/mL). Only 7 patients (1%) had thiamine concentrations below 20 ng/mL (66 nmol/L) on admission. Five of these patients were bedridden and unable to eat food by themselves, and the other two patients used loop diuretics for chronic heart failure. The thiamine concentration declined in most patients (84%) at days 6-8 of admission, regardless of their dietary intake during hospitalization. In conclusion, a low thiamine concentration was not prevalent among newly hospitalized elderly patients with infectious diseases. However, the thiamine concentration significantly decreased during the 6-8 d of hospitalization.


Assuntos
Envelhecimento/sangue , Hospitalização , Infecções/sangue , Tiamina/sangue , Idoso , Idoso de 80 Anos ou mais , Feminino , Hospitais Comunitários/estatística & dados numéricos , Humanos , Japão/epidemiologia , Masculino , Deficiência de Tiamina/epidemiologia
2.
Sex Transm Dis ; 31(3): 192-5, 2004 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-15076934

RESUMO

BACKGROUND: The tiny (T)-strain mycoplasmas, designated in 1974 as Ureaplasma urealyticum, have been divided into 2 species, Ureaplasma parvum (biovar 1) and U. urealyticum (biovar 2), but association of each of these species with nongonococcal urethritis (NGU) remains unclear. GOAL: The goal of this study was to determine whether U. parvum (biovar 1) or U. urealyticum (biovar 2) is associated with NGU. STUDY DESIGN: The prevalences of U. parvum (biovar 1) and U. urealyticum (biovar 2) in 572 patients with urethritis were compared with those in 141 men without urethritis. RESULTS: The prevalence of U. urealyticum (biovar 2) in men with NGU (15.8%) or with nonchlamydial NGU (18.0%) was significantly higher than that in men without urethritis (7.8%). The prevalence of U. parvum (biovar 1) in men with NGU (8.5%) or with nonchlamydial NGU (11.1%) did not differ significantly from that in men without urethritis (13.5%). CONCLUSION: Our results showed a significant association between U. urealyticum (biovar 2) and NGU. They also suggest that the presence of U. parvum (biovar 1) in the male urethra might be the result of colonization.


Assuntos
Infecções por Ureaplasma/epidemiologia , Ureaplasma urealyticum , Uretrite/epidemiologia , Uretrite/microbiologia , Adolescente , Adulto , Idoso , Estudos de Casos e Controles , Infecções por Chlamydia/epidemiologia , Chlamydia trachomatis , Humanos , Japão/epidemiologia , Masculino , Pessoa de Meia-Idade , Prevalência
3.
J Clin Microbiol ; 41(5): 1850-5, 2003 May.
Artigo em Inglês | MEDLINE | ID: mdl-12734216

RESUMO

We present a method for detecting the presence of Mycoplasma genitalium, Mycoplasma hominis, Ureaplasma parvum, and Ureaplasma urealyticum organisms, which are thought to be associated with nongonococcal urethritis (NGU) and other genitourinary infections, in clinical samples. This method consists of PCR amplification of a part of the 16S rRNA gene followed by 96-well microtiter plate hybridization assay using four species-specific capture probes to detect the targets. To test the efficacy of this method, we applied it to the detection of the four species in the urine of patients with NGU. There were no cross-reactions with other human mycoplasmas or ureaplasmas, and the PCR-microtiter plate hybridization assay detected as few as 10 copies of the 16S rRNA gene of each of the four species. Based on these results, this PCR-microtiter plate hybridization assay can be considered an effective tool for the diagnosis of genitourinary infections with mycoplasmas or ureaplasmas.


Assuntos
Infecções por Mycoplasma/diagnóstico , Infecções por Mycoplasma/microbiologia , Reação em Cadeia da Polimerase/métodos , Infecções por Ureaplasma/diagnóstico , Infecções por Ureaplasma/microbiologia , Uretrite/diagnóstico , Uretrite/microbiologia , Técnicas Bacteriológicas/métodos , Técnicas Bacteriológicas/estatística & dados numéricos , Sequência de Bases , DNA Bacteriano/genética , DNA Bacteriano/isolamento & purificação , Humanos , Masculino , Mycoplasma/genética , Mycoplasma/isolamento & purificação , Mycoplasma hominis/genética , Mycoplasma hominis/isolamento & purificação , Hibridização de Ácido Nucleico , Reação em Cadeia da Polimerase/estatística & dados numéricos , RNA Bacteriano/genética , RNA Ribossômico 16S/genética , Sensibilidade e Especificidade , Ureaplasma/genética , Ureaplasma/isolamento & purificação , Ureaplasma urealyticum/genética , Ureaplasma urealyticum/isolamento & purificação
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