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Diversity of the midstream urine microbiome in adults with chronic kidney disease

PURPOSE: To examine the characteristics of the midstream urine microbiome in adults with stage 3–5 non-dialysis-dependent chronic kidney disease (CKD). METHODS: Patients with non-dialysis-dependent CKD (estimated glomerular filtration rate [eGFR] < 60 ml/min/1.73 m(2)) and diuretic use were recru...

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Autores principales: Kramer, Holly, Kuffel, Gina, Thomas-White, Krystal, Wolfe, Alan J., Vellanki, Kavitha, Leehey, David J., Bansal, Vinod K., Brubaker, Linda, Flanigan, Robert, Koval, Julia, Wadhwa, Anuradha, Zilliox, Michael J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5986845/
https://www.ncbi.nlm.nih.gov/pubmed/29651696
http://dx.doi.org/10.1007/s11255-018-1860-7
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author Kramer, Holly
Kuffel, Gina
Thomas-White, Krystal
Wolfe, Alan J.
Vellanki, Kavitha
Leehey, David J.
Bansal, Vinod K.
Brubaker, Linda
Flanigan, Robert
Koval, Julia
Wadhwa, Anuradha
Zilliox, Michael J.
author_facet Kramer, Holly
Kuffel, Gina
Thomas-White, Krystal
Wolfe, Alan J.
Vellanki, Kavitha
Leehey, David J.
Bansal, Vinod K.
Brubaker, Linda
Flanigan, Robert
Koval, Julia
Wadhwa, Anuradha
Zilliox, Michael J.
author_sort Kramer, Holly
collection PubMed
description PURPOSE: To examine the characteristics of the midstream urine microbiome in adults with stage 3–5 non-dialysis-dependent chronic kidney disease (CKD). METHODS: Patients with non-dialysis-dependent CKD (estimated glomerular filtration rate [eGFR] < 60 ml/min/1.73 m(2)) and diuretic use were recruited from outpatient nephrology clinics. Midstream voided urine specimens were collected using the clean-catch method. The bacterial composition was determined by sequencing the hypervariable (V4) region of the bacterial 16S ribosomal RNA gene. Extraction negative controls (no urine) were included to assess the contribution of extraneous DNA from possible sources of contamination. Midstream urine microbiome diversity was assessed with the inverse Simpson, Chao and Shannon indices. The diversity measures were further examined by demographic characteristics and by comorbidities. RESULTS: The cohort of 41 women and 36 men with detectable bacterial DNA in their urine samples had a mean age of 71.5 years (standard deviation [SD] 7.9) years (range 60–91 years). The majority were white (68.0%) and a substantial minority were African-American (29.3%) The mean eGFR was 27.2 (SD 13.6) ml/min/1.73 m(2). Most men (72.2%) were circumcised and 16.6% reported a remote history of prostate cancer. Many midstream voided urine specimens were dominated (> 50% reads) by the genera Corynebacterium (n = 11), Staphylococcus (n = 9), Streptococcus (n = 7), Lactobacillus (n = 7), Gardnerella (n = 7), Prevotella (n = 4), Escherichia_Shigella (n = 3), and Enterobacteriaceae (n = 2); the rest lacked a dominant genus. The samples had high levels of diversity, as measured by the inverse Simpson [7.24 (95% CI 6.76, 7.81)], Chao [558.24 (95% CI 381.70, 879.35)], and Shannon indices [2.60 (95% CI 2.51, 2.69)]. Diversity measures were generally higher in participants with urgency urinary incontinence and higher estimated glomerular filtration rate (eGFR). After controlling for demographics and diabetes status, microbiome diversity was significantly associated with estimated eGFR (P < 0.05). CONCLUSIONS: The midstream voided urine microbiome of older adults with stage 3–5 non-dialysis-dependent CKD is diverse. Greater microbiome diversity is associated with higher eGFR.
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spelling pubmed-59868452018-06-12 Diversity of the midstream urine microbiome in adults with chronic kidney disease Kramer, Holly Kuffel, Gina Thomas-White, Krystal Wolfe, Alan J. Vellanki, Kavitha Leehey, David J. Bansal, Vinod K. Brubaker, Linda Flanigan, Robert Koval, Julia Wadhwa, Anuradha Zilliox, Michael J. Int Urol Nephrol Nephrology - Original Paper PURPOSE: To examine the characteristics of the midstream urine microbiome in adults with stage 3–5 non-dialysis-dependent chronic kidney disease (CKD). METHODS: Patients with non-dialysis-dependent CKD (estimated glomerular filtration rate [eGFR] < 60 ml/min/1.73 m(2)) and diuretic use were recruited from outpatient nephrology clinics. Midstream voided urine specimens were collected using the clean-catch method. The bacterial composition was determined by sequencing the hypervariable (V4) region of the bacterial 16S ribosomal RNA gene. Extraction negative controls (no urine) were included to assess the contribution of extraneous DNA from possible sources of contamination. Midstream urine microbiome diversity was assessed with the inverse Simpson, Chao and Shannon indices. The diversity measures were further examined by demographic characteristics and by comorbidities. RESULTS: The cohort of 41 women and 36 men with detectable bacterial DNA in their urine samples had a mean age of 71.5 years (standard deviation [SD] 7.9) years (range 60–91 years). The majority were white (68.0%) and a substantial minority were African-American (29.3%) The mean eGFR was 27.2 (SD 13.6) ml/min/1.73 m(2). Most men (72.2%) were circumcised and 16.6% reported a remote history of prostate cancer. Many midstream voided urine specimens were dominated (> 50% reads) by the genera Corynebacterium (n = 11), Staphylococcus (n = 9), Streptococcus (n = 7), Lactobacillus (n = 7), Gardnerella (n = 7), Prevotella (n = 4), Escherichia_Shigella (n = 3), and Enterobacteriaceae (n = 2); the rest lacked a dominant genus. The samples had high levels of diversity, as measured by the inverse Simpson [7.24 (95% CI 6.76, 7.81)], Chao [558.24 (95% CI 381.70, 879.35)], and Shannon indices [2.60 (95% CI 2.51, 2.69)]. Diversity measures were generally higher in participants with urgency urinary incontinence and higher estimated glomerular filtration rate (eGFR). After controlling for demographics and diabetes status, microbiome diversity was significantly associated with estimated eGFR (P < 0.05). CONCLUSIONS: The midstream voided urine microbiome of older adults with stage 3–5 non-dialysis-dependent CKD is diverse. Greater microbiome diversity is associated with higher eGFR. Springer Netherlands 2018-04-12 2018 /pmc/articles/PMC5986845/ /pubmed/29651696 http://dx.doi.org/10.1007/s11255-018-1860-7 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Nephrology - Original Paper
Kramer, Holly
Kuffel, Gina
Thomas-White, Krystal
Wolfe, Alan J.
Vellanki, Kavitha
Leehey, David J.
Bansal, Vinod K.
Brubaker, Linda
Flanigan, Robert
Koval, Julia
Wadhwa, Anuradha
Zilliox, Michael J.
Diversity of the midstream urine microbiome in adults with chronic kidney disease
title Diversity of the midstream urine microbiome in adults with chronic kidney disease
title_full Diversity of the midstream urine microbiome in adults with chronic kidney disease
title_fullStr Diversity of the midstream urine microbiome in adults with chronic kidney disease
title_full_unstemmed Diversity of the midstream urine microbiome in adults with chronic kidney disease
title_short Diversity of the midstream urine microbiome in adults with chronic kidney disease
title_sort diversity of the midstream urine microbiome in adults with chronic kidney disease
topic Nephrology - Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5986845/
https://www.ncbi.nlm.nih.gov/pubmed/29651696
http://dx.doi.org/10.1007/s11255-018-1860-7
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