Cargando…

Association of Admission Functional Status and Body Mass Index with Mortality in Patients Receiving Chronic Dialysis: A Nationwide Observational Cohort Study

INTRODUCTION: Chronic kidney disease (CKD) significantly affects activities of daily living (ADLs) before and after the initiation of dialysis, particularly in elderly individuals. However, the impact of admission functional status on dialysis patients’ outcome is not fully understood. This study ai...

Descripción completa

Detalles Bibliográficos
Autores principales:	Mandai, Shintaro, Koide, Takaaki, Fujiki, Tamami, Mori, Yutaro, Ando, Fumiaki, Susa, Koichiro, Mori, Takayasu, Iimori, Soichiro, Naito, Shotaro, Sohara, Eisei, Uchida, Shinichi, Fushimi, Kiyohide, Rai, Tatemitsu
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Japan Medical Association 2023
Materias:	Original Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10628309/ https://www.ncbi.nlm.nih.gov/pubmed/37941718 http://dx.doi.org/10.31662/jmaj.2022-0188

Ejemplares similares

Burden of kidney disease on the discrepancy between reasons for hospital admission and death: An observational cohort study
por: Mandai, Shintaro, et al.
Publicado: (2021)

ZNF185 prevents stress fiber formation through the inhibition of RhoA in endothelial cells
por: Suzuki, Soichiro, et al.
Publicado: (2023)

Dialysis Case Volume Associated With In-Hospital Mortality in Maintenance Dialysis Patients
por: Mandai, Shintaro, et al.
Publicado: (2017)

Chronic kidney disease causes blood-brain barrier breakdown via urea-activated matrix metalloproteinase-2 and insolubility of tau protein
por: Matsuki, Hisazumi, et al.
Publicado: (2023)

Short-term prognosis of emergently hospitalized dialysis-independent chronic kidney disease patients: A nationwide retrospective cohort study in Japan
por: Kikuchi, Hiroaki, et al.
Publicado: (2018)

Tolvaptan activates the Nrf2/HO-1 antioxidant pathway through PERK phosphorylation
por: Fujiki, Tamami, et al.
Publicado: (2019)

Rapidly progressive IgA nephropathy with membranoproliferative glomerulonephritis-like lesions in an elderly man following the third dose of an mRNA COVID-19 vaccine: a case report
por: Morimoto, Nobuhisa, et al.
Publicado: (2023)

LRBA is essential for urinary concentration and body water homeostasis
por: Hara, Yu, et al.
Publicado: (2022)

Deletion of Alox15 improves kidney dysfunction and inhibits fibrosis by increased PGD(2) in the kidney
por: Takahashi, Naohiro, et al.
Publicado: (2021)

Loop diuretics are associated with greater risk of sarcopenia in patients with non-dialysis-dependent chronic kidney disease
por: Ishikawa, Seiko, et al.
Publicado: (2018)

Sodium–calcium exchanger 1 is the key molecule for urinary potassium excretion against acute hyperkalemia
por: Shoda, Wakana, et al.
Publicado: (2020)

Prognosis of chronic kidney disease with normal-range proteinuria: The CKD-ROUTE study
por: Iimori, Soichiro, et al.
Publicado: (2018)

The proteasome inhibitor bortezomib attenuates renal fibrosis in mice via the suppression of TGF-β1
por: Zeniya, Moko, et al.
Publicado: (2017)

WNK1 regulates skeletal muscle cell hypertrophy by modulating the nuclear localization and transcriptional activity of FOXO4
por: Mandai, Shintaro, et al.
Publicado: (2018)

NCC regulation by WNK signal cascade
por: Uchida, Shinichi, et al.
Publicado: (2023)

Loop diuretics affect skeletal myoblast differentiation and exercise-induced muscle hypertrophy
por: Mandai, Shintaro, et al.
Publicado: (2017)

Drug-Repositioning Screening for Keap1-Nrf2 Binding Inhibitors using Fluorescence Correlation Spectroscopy
por: Yoshizaki, Yuki, et al.
Publicado: (2017)

Acute poststreptococcal glomerulonephritis with acute interstitial nephritis related to streptococcal pyrogenic exotoxin B
por: Ando, Fumiaki, et al.
Publicado: (2013)

Wnt5a induces renal AQP2 expression by activating calcineurin signalling pathway
por: Ando, Fumiaki, et al.
Publicado: (2016)

AKAPs-PKA disruptors increase AQP2 activity independently of vasopressin in a model of nephrogenic diabetes insipidus
por: Ando, Fumiaki, et al.
Publicado: (2018)

Regulation of with-no-lysine kinase signaling by Kelch-like proteins
por: Uchida, Shinichi, et al.
Publicado: (2014)

Genetic Background and Clinicopathologic Features of Adult-onset Nephronophthisis
por: Fujimaru, Takuya, et al.
Publicado: (2021)

Encephalopathy Induced by High Plasma and Cerebrospinal Fluid Ceftriaxone Concentrations in a Hemodialysis Patient
por: Suzuki, Soichiro, et al.
Publicado: (2019)

Generation and analysis of knock-in mice carrying pseudohypoaldosteronism type II-causing mutations in the cullin 3 gene
por: Araki, Yuya, et al.
Publicado: (2015)

Role of ClC-K and barttin in low potassium-induced sodium chloride cotransporter activation and hypertension in mouse kidney
por: Nomura, Naohiro, et al.
Publicado: (2018)

Inherited, not acquired, Gitelman syndrome in a patient with Sjögren’s syndrome: importance of genetic testing to distinguish the two forms
por: Mishima, Eikan, et al.
Publicado: (2017)

WNK4 is the major WNK positively regulating NCC in the mouse kidney
por: Takahashi, Daiei, et al.
Publicado: (2014)

Acquired Gitelman Syndrome in an Anti-SSA Antibody-positive Patient with a SLC12A3 Heterozygous Mutation
por: Kusuda, Takeshi, et al.
Publicado: (2016)

Fibronectin glomerulopathy
por: Ishimoto, Ikue, et al.
Publicado: (2013)

WNK4 is an Adipogenic Factor and Its Deletion Reduces Diet-Induced Obesity in Mice
por: Takahashi, Daiei, et al.
Publicado: (2017)

Salt suppresses IFNγ inducible chemokines through the IFNγ-JAK1-STAT1 signaling pathway in proximal tubular cells
por: Arai, Yohei, et al.
Publicado: (2017)

A case of Gitelman syndrome: our experience with a patient treated in clinical practice on a local island
por: Chinen, Takashi, et al.
Publicado: (2019)

Congenital nephrogenic diabetes insipidus presenting as osmotic demyelination syndrome in infancy: A case report
por: Kobayashi, Satoru, et al.
Publicado: (2022)

Acute Insulin Stimulation Induces Phosphorylation of the Na-Cl Cotransporter in Cultured Distal mpkDCT Cells and Mouse Kidney
por: Sohara, Eisei, et al.
Publicado: (2011)

Case of hereditary kidney disease presenting thin basement membrane with a single heterozygous variant of Intersectin 2
por: Kondo, Madoka, et al.
Publicado: (2023)

A minor role of WNK3 in regulating phosphorylation of renal NKCC2 and NCC co-transporters in vivo
por: Oi, Katsuyuki, et al.
Publicado: (2011)

A novel SLC5A2 heterozygous variant in a family with familial renal glucosuria
por: Hatano, Maho, et al.
Publicado: (2022)

Non-urate transporter 1, non-glucose transporter member 9-related renal hypouricemia and acute renal failure accompanied by hyperbilirubinemia after anaerobic exercise: a case report
por: Furuto, Yoshitaka, et al.
Publicado: (2019)

Transplantation of a kidney with a heterozygous mutation in the SLC22A12 (URAT1) gene causing renal hypouricemia: a case report
por: Tsuji, Kiyokazu, et al.
Publicado: (2020)

Infective endocarditis in a patient with lupus nephritis who was undergoing immunosuppressive therapy: A case of survival
por: Ihara, Katsuhito, et al.
Publicado: (2017)

Cannot write session to /tmp/vufind_sessions/sess_lomnjrfpdp1t7b0felpgmf3heb