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Impacts of Sex Differences in Pulse Pressure among Patients with Chronic Kidney Disease
Introduction: Though disease-related differences between the sexes have increasingly attracted attention, the renal impact of pulse pressure (PP) in patients with chronic kidney disease (CKD) has never been investigated comprehensively in relation to differences associated with sex. We aimed to exam...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6963663/ https://www.ncbi.nlm.nih.gov/pubmed/31835400 http://dx.doi.org/10.3390/jpm9040052 |
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author | Kataoka, Hiroshi Sawara, Yukako Kawachi, Keiko Manabe, Shun Mochizuki, Toshio Nitta, Kosaku |
author_facet | Kataoka, Hiroshi Sawara, Yukako Kawachi, Keiko Manabe, Shun Mochizuki, Toshio Nitta, Kosaku |
author_sort | Kataoka, Hiroshi |
collection | PubMed |
description | Introduction: Though disease-related differences between the sexes have increasingly attracted attention, the renal impact of pulse pressure (PP) in patients with chronic kidney disease (CKD) has never been investigated comprehensively in relation to differences associated with sex. We aimed to examine sex differences in PP as a related factor of CKD progression from the perspective of atherosclerosis. Methods: A total of 156 patients with CKD matched according to age and estimated glomerular filtration rate (eGFR) were separated into sex-based cohorts. Multivariate Cox proportional hazards analyses were performed to identify factors associated with renal outcomes. Kaplan–Meier analyses were performed to assess disease progression, which was defined as a ≥50% estimated glomerular filtration rate (eGFR) decline or end-stage renal disease. Results: The mean age of the study participants was 58.9 ± 13.1 years, and the median follow-up period was 114.0 months. A multivariate Cox regression analysis showed that PP was significantly associated with disease progression among the entire cohort (p = 0.007). In the sex-based sub-cohort analyses, PP was significantly associated with disease progression in men (p = 0.0004) but not in women. Among the entire cohort, PP was correlated positively with age (p = 0.03) and negatively with high-density lipoprotein-cholesterol (HDL-C) level (p = 0.003). PP was significantly correlated with visceral fat area (VFA) (p = 0.04) and hemoglobin level (p = 0.04) in men and with HDL-C level (p = 0.003) in women. Conclusion: A high PP is a significant related factor of CKD progression, especially in men, in whom it is significantly associated with greater VFA and lower hemoglobin level. |
format | Online Article Text |
id | pubmed-6963663 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-69636632020-01-27 Impacts of Sex Differences in Pulse Pressure among Patients with Chronic Kidney Disease Kataoka, Hiroshi Sawara, Yukako Kawachi, Keiko Manabe, Shun Mochizuki, Toshio Nitta, Kosaku J Pers Med Article Introduction: Though disease-related differences between the sexes have increasingly attracted attention, the renal impact of pulse pressure (PP) in patients with chronic kidney disease (CKD) has never been investigated comprehensively in relation to differences associated with sex. We aimed to examine sex differences in PP as a related factor of CKD progression from the perspective of atherosclerosis. Methods: A total of 156 patients with CKD matched according to age and estimated glomerular filtration rate (eGFR) were separated into sex-based cohorts. Multivariate Cox proportional hazards analyses were performed to identify factors associated with renal outcomes. Kaplan–Meier analyses were performed to assess disease progression, which was defined as a ≥50% estimated glomerular filtration rate (eGFR) decline or end-stage renal disease. Results: The mean age of the study participants was 58.9 ± 13.1 years, and the median follow-up period was 114.0 months. A multivariate Cox regression analysis showed that PP was significantly associated with disease progression among the entire cohort (p = 0.007). In the sex-based sub-cohort analyses, PP was significantly associated with disease progression in men (p = 0.0004) but not in women. Among the entire cohort, PP was correlated positively with age (p = 0.03) and negatively with high-density lipoprotein-cholesterol (HDL-C) level (p = 0.003). PP was significantly correlated with visceral fat area (VFA) (p = 0.04) and hemoglobin level (p = 0.04) in men and with HDL-C level (p = 0.003) in women. Conclusion: A high PP is a significant related factor of CKD progression, especially in men, in whom it is significantly associated with greater VFA and lower hemoglobin level. MDPI 2019-12-09 /pmc/articles/PMC6963663/ /pubmed/31835400 http://dx.doi.org/10.3390/jpm9040052 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Kataoka, Hiroshi Sawara, Yukako Kawachi, Keiko Manabe, Shun Mochizuki, Toshio Nitta, Kosaku Impacts of Sex Differences in Pulse Pressure among Patients with Chronic Kidney Disease |
title | Impacts of Sex Differences in Pulse Pressure among Patients with Chronic Kidney Disease |
title_full | Impacts of Sex Differences in Pulse Pressure among Patients with Chronic Kidney Disease |
title_fullStr | Impacts of Sex Differences in Pulse Pressure among Patients with Chronic Kidney Disease |
title_full_unstemmed | Impacts of Sex Differences in Pulse Pressure among Patients with Chronic Kidney Disease |
title_short | Impacts of Sex Differences in Pulse Pressure among Patients with Chronic Kidney Disease |
title_sort | impacts of sex differences in pulse pressure among patients with chronic kidney disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6963663/ https://www.ncbi.nlm.nih.gov/pubmed/31835400 http://dx.doi.org/10.3390/jpm9040052 |
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