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1.
J Ren Nutr ; 30(1): 31-35, 2020 01.
Article in English | MEDLINE | ID: mdl-30956092

ABSTRACT

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.


Subject(s)
Constipation/complications , Cresols/blood , Cresols/urine , Indican/blood , Indican/urine , Renal Insufficiency, Chronic/complications , Sulfuric Acid Esters/blood , Sulfuric Acid Esters/urine , Constipation/blood , Constipation/urine , Cross-Sectional Studies , Defecation , Female , Humans , Male , Middle Aged , Renal Insufficiency, Chronic/blood , Renal Insufficiency, Chronic/urine
2.
Food Funct ; 9(12): 6508-6516, 2018 Dec 13.
Article in English | MEDLINE | ID: mdl-30468238

ABSTRACT

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.


Subject(s)
Cresols/urine , Indican/urine , Oxidative Stress/drug effects , Prebiotics/administration & dosage , Renal Insufficiency, Chronic/diet therapy , Starch/metabolism , Sulfuric Acid Esters/urine , Adult , Anthropometry , Biomarkers/blood , Biomarkers/urine , C-Reactive Protein/metabolism , Female , Humans , Interleukin-6/blood , Male , Middle Aged , Pilot Projects , Renal Dialysis , Renal Insufficiency, Chronic/blood , Renal Insufficiency, Chronic/therapy , Renal Insufficiency, Chronic/urine , Thiobarbituric Acid Reactive Substances/metabolism , Urine/chemistry , Zea mays/chemistry , Zea mays/metabolism
4.
Bol. méd. Hosp. Infant. Méx ; 44(7): 402-4, jul. 1987. tab
Article in Spanish | LILACS | ID: lil-46881

ABSTRACT

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


Subject(s)
Child, Preschool , Child , Adolescent , Indican/urine , Intestines/microbiology , Respiratory Function Tests , Tinidazole/pharmacology , Hydrogen/analysis , Tinidazole/urine
6.
Bol Med Hosp Infant Mex ; 35(1): 137-44, 1978.
Article in Spanish | MEDLINE | ID: mdl-339926

ABSTRACT

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.


Subject(s)
Indican/urine , Kwashiorkor/urine , Analysis of Variance , Animals , Cattle , Creatinine/urine , Diarrhea, Infantile/metabolism , Diarrhea, Infantile/urine , Diet Therapy , Escherichia coli/metabolism , Female , Humans , Infant , Intestine, Small/microbiology , Kwashiorkor/metabolism , Kwashiorkor/therapy , Male , Milk/metabolism , Tryptophan/metabolism
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