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Interdialytic Weight Gain Effects on Hemoglobin Concentration and Cardiovascular Events
INTRODUCTION: Although predialysis hemoglobin concentration is affected by interdialytic weight gain (IDWG), the interaction between these parameters is not well understood. METHODS: Using data from the Japanese Dialysis Outcomes and Practice Pattern Study phases 1–5, we analyzed patients who underw...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7572305/ https://www.ncbi.nlm.nih.gov/pubmed/33102959 http://dx.doi.org/10.1016/j.ekir.2020.07.027 |
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author | Hara, Takashi Kimachi, Miho Akizawa, Tadao Fukuhara, Shunichi Yamamoto, Yosuke |
author_facet | Hara, Takashi Kimachi, Miho Akizawa, Tadao Fukuhara, Shunichi Yamamoto, Yosuke |
author_sort | Hara, Takashi |
collection | PubMed |
description | INTRODUCTION: Although predialysis hemoglobin concentration is affected by interdialytic weight gain (IDWG), the interaction between these parameters is not well understood. METHODS: Using data from the Japanese Dialysis Outcomes and Practice Pattern Study phases 1–5, we analyzed patients who underwent maintenance hemodialysis. The exposure variable was hemoglobin concentration, and the effect modifier was IDWG at baseline. These 2 categorical variables were then combined and analyzed. The primary outcome was major adverse cardiovascular events (MACEs). Hazard ratios were estimated using a Cox model for the association between exposure and MACEs after adjusting for potential confounders. We examined additive interactions between hemoglobin concentration and IDWG by calculating the relative excess risk due to interaction, which is defined as a departure from the additivity of effects. RESULTS: A total of 8234 patients were enrolled. During a median follow-up of 2.1 years, 1062 (12.9%) patients developed MACEs. In IDWG categories of <6%, adjusted hazard ratios for MACEs tended to be lower as hemoglobin concentration increased. In IDWG categories of ≥6%, point estimation of MACEs with hemoglobin concentration of ≥11.0 g/dl–<12.0 g/dl was higher than that with hemoglobin concentration of ≥10.0 g/dl–<11.0 g/dl. The relative excess risk due to interaction was 0.22 (95% confidence interval 0.02–0.42) between IDWG category of ≥6% and hemoglobin categories of ≥11.0 g/dl–<12.0 g/dl, indicating a synergistic interaction. CONCLUSIONS: The association between hemoglobin concentration and MACEs differed across IDWG. Consideration should be given to the upper limit of hemoglobin concentration in patients with high IDWG. |
format | Online Article Text |
id | pubmed-7572305 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-75723052020-10-23 Interdialytic Weight Gain Effects on Hemoglobin Concentration and Cardiovascular Events Hara, Takashi Kimachi, Miho Akizawa, Tadao Fukuhara, Shunichi Yamamoto, Yosuke Kidney Int Rep Clinical Research INTRODUCTION: Although predialysis hemoglobin concentration is affected by interdialytic weight gain (IDWG), the interaction between these parameters is not well understood. METHODS: Using data from the Japanese Dialysis Outcomes and Practice Pattern Study phases 1–5, we analyzed patients who underwent maintenance hemodialysis. The exposure variable was hemoglobin concentration, and the effect modifier was IDWG at baseline. These 2 categorical variables were then combined and analyzed. The primary outcome was major adverse cardiovascular events (MACEs). Hazard ratios were estimated using a Cox model for the association between exposure and MACEs after adjusting for potential confounders. We examined additive interactions between hemoglobin concentration and IDWG by calculating the relative excess risk due to interaction, which is defined as a departure from the additivity of effects. RESULTS: A total of 8234 patients were enrolled. During a median follow-up of 2.1 years, 1062 (12.9%) patients developed MACEs. In IDWG categories of <6%, adjusted hazard ratios for MACEs tended to be lower as hemoglobin concentration increased. In IDWG categories of ≥6%, point estimation of MACEs with hemoglobin concentration of ≥11.0 g/dl–<12.0 g/dl was higher than that with hemoglobin concentration of ≥10.0 g/dl–<11.0 g/dl. The relative excess risk due to interaction was 0.22 (95% confidence interval 0.02–0.42) between IDWG category of ≥6% and hemoglobin categories of ≥11.0 g/dl–<12.0 g/dl, indicating a synergistic interaction. CONCLUSIONS: The association between hemoglobin concentration and MACEs differed across IDWG. Consideration should be given to the upper limit of hemoglobin concentration in patients with high IDWG. Elsevier 2020-07-27 /pmc/articles/PMC7572305/ /pubmed/33102959 http://dx.doi.org/10.1016/j.ekir.2020.07.027 Text en © 2020 International Society of Nephrology. Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Clinical Research Hara, Takashi Kimachi, Miho Akizawa, Tadao Fukuhara, Shunichi Yamamoto, Yosuke Interdialytic Weight Gain Effects on Hemoglobin Concentration and Cardiovascular Events |
title | Interdialytic Weight Gain Effects on Hemoglobin Concentration and Cardiovascular Events |
title_full | Interdialytic Weight Gain Effects on Hemoglobin Concentration and Cardiovascular Events |
title_fullStr | Interdialytic Weight Gain Effects on Hemoglobin Concentration and Cardiovascular Events |
title_full_unstemmed | Interdialytic Weight Gain Effects on Hemoglobin Concentration and Cardiovascular Events |
title_short | Interdialytic Weight Gain Effects on Hemoglobin Concentration and Cardiovascular Events |
title_sort | interdialytic weight gain effects on hemoglobin concentration and cardiovascular events |
topic | Clinical Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7572305/ https://www.ncbi.nlm.nih.gov/pubmed/33102959 http://dx.doi.org/10.1016/j.ekir.2020.07.027 |
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