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1.
J Ren Nutr ; 30(1): 31-35, 2020 01.
Artigo em Inglês | MEDLINE | ID: mdl-30956092

RESUMO

OBJECTIVE: The aim of this study is to evaluate the association between bowel habits and microbial-derived uremic toxins p-cresyl sulfate (PCS) and indoxyl sulfate (IS) in patients with non-dialysis-dependent chronic kidney disease (NDD-CKD). DESIGN AND METHODS: This is a cross-sectional analysis including 43 nondiabetic NDD-CKD patients (58% men; 59.0 ± 13.5 years; estimated glomerular filtration rate, 21.3 ± 7.9 mL/min/1.73 m2). Bowel habit was assessed by the Bristol Stool Scale (BSS <3, characterized by hard consistency of stools and/or low frequency of evacuation and BSS ≥3, representing a more regular bowel habit) and by the Rome III criteria. PCS and IS (serum, free and total; urinary, total) were determined by high-performance liquid chromatography. Dietary intake was assessed by the 3-day food records. RESULTS: The frequency of constipation assessed by BSS and Rome III criteria was 33% (n = 14/43) and 35% (n = 15/43), respectively. The BSS <3 exhibited higher PCS, independent of renal function and dietary protein-fiber ratio (ß [95% confidence interval {CI}]: serum, total PCS = 1.54 [1.06-2.23], P = .02; serum free PCS = 1.40 [1.00-1.97], P = .05; urinary PCS = 1.78 [1.10-2.90], P < .02). According to the Rome III criteria, a tendency for a higher serum total PCS (ß [95% CI]: 1.39 [0.95-2.03 µmol/L], P = .09) and a significantly higher urinary PCS (ß [95% CI]: 1.80 [1.11-2.94 µmol/24 h], P = .02) was found in constipated participants. No effect of a compromised bowel habit (Rome III criteria or BSS) was found on IS. CONCLUSION: Constipation may lead to production of PCS in nondiabetic NDD-CKD patients.


Assuntos
Constipação Intestinal/complicações , Cresóis/sangue , Cresóis/urina , Indicã/sangue , Indicã/urina , Insuficiência Renal Crônica/complicações , Ésteres do Ácido Sulfúrico/sangue , Ésteres do Ácido Sulfúrico/urina , Constipação Intestinal/sangue , Constipação Intestinal/urina , Estudos Transversais , Defecação , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Insuficiência Renal Crônica/sangue , Insuficiência Renal Crônica/urina
2.
Food Funct ; 9(12): 6508-6516, 2018 Dec 13.
Artigo em Inglês | MEDLINE | ID: mdl-30468238

RESUMO

An imbalance of gut microbiota is considered a new cardiovascular risk factor for chronic kidney disease (CKD) patients, since it is directly associated with increased uremic toxin production, inflammation and oxidative stress. Strategies such as prebiotic supplementation have been suggested to mitigate these complications. We hypothesized that prebiotic-resistant starch could ameliorate uremic toxins levels, oxidative stress, and inflammatory states in hemodialysis (HD) patients. This pilot study evaluated 31 HD patients assigned to either resistant starch (16 g of resistant starch Hi-Maize® 260) or placebo (manioc flour) supplementation, which they received for 4 weeks on alternate days through cookies on dialysis days and powder in a sachet on non-dialysis days. Levels of interleukin (IL)-6, high-sensitive C-reactive protein, thiobarbituric acid reactive substances plasma (TBARS), protein carbonylation, indoxyl sulfate (IS) and p-cresyl sulfate were measured. Anthropometric and biochemical parameters, as well as, food intake were also evaluated. As expected, resistant starch group increased fiber intake (p > 0.01), in addition the prebiotic supplementation reduced IL-6 (p = 0.01), TBARS (p > 0.01), and IS (p > 0.01) plasma levels. No significant differences were evident in the placebo group. Prebiotic-resistant starch supplementation seems to be a promising nutritional strategy to improve inflammation, oxidative stress and to reduce IS plasma levels in CKD patients on HD.


Assuntos
Cresóis/urina , Indicã/urina , Estresse Oxidativo/efeitos dos fármacos , Prebióticos/administração & dosagem , Insuficiência Renal Crônica/dietoterapia , Amido/metabolismo , Ésteres do Ácido Sulfúrico/urina , Adulto , Antropometria , Biomarcadores/sangue , Biomarcadores/urina , Proteína C-Reativa/metabolismo , Feminino , Humanos , Interleucina-6/sangue , Masculino , Pessoa de Meia-Idade , Projetos Piloto , Diálise Renal , Insuficiência Renal Crônica/sangue , Insuficiência Renal Crônica/terapia , Insuficiência Renal Crônica/urina , Substâncias Reativas com Ácido Tiobarbitúrico/metabolismo , Urina/química , Zea mays/química , Zea mays/metabolismo
4.
Bol. méd. Hosp. Infant. Méx ; 44(7): 402-4, jul. 1987. tab
Artigo em Espanhol | LILACS | ID: lil-46881

RESUMO

Con objeto de investigar si el efecto antimicrobiano del tinidazol modifica los resultados obtenidos con la prueba del hidrógeno espirado, siete días despupes de haber tomado una dosis de este medicamento, se realizó un estudio en escolares clínicamente sanos y bien nutridos. Los resultados no mostraron diferencias significativas entre las observaciones hachas antes y siete días después de dar el tinidazol. La excresión de indican tampoco mostró cambios significativos, lo cual indirectamente hace suponer que de haber acontecido algún cambio en la flora bacteriana intestinal por efecto del medicamento, una semana después ya se había recuperado


Assuntos
Pré-Escolar , Criança , Adolescente , Indicã/urina , Intestinos/microbiologia , Testes de Função Respiratória , Tinidazol/farmacologia , Hidrogênio/análise , Tinidazol/urina
6.
Bol Med Hosp Infant Mex ; 35(1): 137-44, 1978.
Artigo em Espanhol | MEDLINE | ID: mdl-339926

RESUMO

Most indican excreted in the urine comes from the degradation of tryptophan through the action of microorganisms dwelling within the intestinal lumen. Based on this knowledge, the excretion of this compound was investigated during the recovery process of 19 malnourished infants; thus, attempts were made to recognize indirectly whether quantitative modifications take place in the intestinal flora as the state of nutrition is re-established. The results do not suggest the presence of an important variation of the bacterial content within the intestine of these children, at least during the first four weeks of their recovery.


Assuntos
Indicã/urina , Kwashiorkor/urina , Análise de Variância , Animais , Bovinos , Creatinina/urina , Diarreia Infantil/metabolismo , Diarreia Infantil/urina , Dietoterapia , Escherichia coli/metabolismo , Feminino , Humanos , Lactente , Intestino Delgado/microbiologia , Kwashiorkor/metabolismo , Kwashiorkor/terapia , Masculino , Leite/metabolismo , Triptofano/metabolismo
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