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Progranulin and Its Receptor Predict Kidney Function Decline in Patients With Type 2 Diabetes
Progranulin (PGRN), a growth factor, is abundantly expressed in a broad range of tissues and cell types with pleiotropic functions including inflammation, neurodegeneration, and facilitating lysosome acidification. PGRN binds to TNF receptors (TNFR) and inhibits downstream inflammatory signaling pat...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9012489/ https://www.ncbi.nlm.nih.gov/pubmed/35432201 http://dx.doi.org/10.3389/fendo.2022.849457 |
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author | Murakoshi, Maki Gohda, Tomohito Sakuma, Hiroko Shibata, Terumi Adachi, Eri Kishida, Chiaki Ichikawa, Saki Koshida, Takeo Kamei, Nozomu Suzuki, Yusuke |
author_facet | Murakoshi, Maki Gohda, Tomohito Sakuma, Hiroko Shibata, Terumi Adachi, Eri Kishida, Chiaki Ichikawa, Saki Koshida, Takeo Kamei, Nozomu Suzuki, Yusuke |
author_sort | Murakoshi, Maki |
collection | PubMed |
description | Progranulin (PGRN), a growth factor, is abundantly expressed in a broad range of tissues and cell types with pleiotropic functions including inflammation, neurodegeneration, and facilitating lysosome acidification. PGRN binds to TNF receptors (TNFR) and inhibits downstream inflammatory signaling pathways. TNFR is a well-known predictor of glomerular filtration rate (GFR) decline in a variety of diseases. Therefore, we measured circulating PGRN in addition to TNFR using an enzyme-linked immunosorbent assay and explored whether it predicted renal prognosis in 201 Japanese patients with type 2 diabetes. During a median follow-up of 7.6 years, 21 participants reached primary renal endpoint, which involves a decline of at least 57% in eGFR from baseline, or the onset of end-stage renal disease. Univariate Cox regression analysis revealed that classical renal measures (GFR and albuminuria), two TNF-related biomarkers (PGRN and TNFR), and BMI were associated with this outcome. Multivariate analysis demonstrated that high levels of PGRN [HR 2.50 (95%CI 2.47–2.52)] or TNFR1 [HR 5.38 (95%CI 5.26–5.50)] were associated with this outcome after adjusting for relevant covariates. The high levels of PGRN as well as TNFR1 were associated with a risk of primary renal outcome in patients with type 2 diabetes after adjusting for established risk factors. |
format | Online Article Text |
id | pubmed-9012489 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90124892022-04-16 Progranulin and Its Receptor Predict Kidney Function Decline in Patients With Type 2 Diabetes Murakoshi, Maki Gohda, Tomohito Sakuma, Hiroko Shibata, Terumi Adachi, Eri Kishida, Chiaki Ichikawa, Saki Koshida, Takeo Kamei, Nozomu Suzuki, Yusuke Front Endocrinol (Lausanne) Endocrinology Progranulin (PGRN), a growth factor, is abundantly expressed in a broad range of tissues and cell types with pleiotropic functions including inflammation, neurodegeneration, and facilitating lysosome acidification. PGRN binds to TNF receptors (TNFR) and inhibits downstream inflammatory signaling pathways. TNFR is a well-known predictor of glomerular filtration rate (GFR) decline in a variety of diseases. Therefore, we measured circulating PGRN in addition to TNFR using an enzyme-linked immunosorbent assay and explored whether it predicted renal prognosis in 201 Japanese patients with type 2 diabetes. During a median follow-up of 7.6 years, 21 participants reached primary renal endpoint, which involves a decline of at least 57% in eGFR from baseline, or the onset of end-stage renal disease. Univariate Cox regression analysis revealed that classical renal measures (GFR and albuminuria), two TNF-related biomarkers (PGRN and TNFR), and BMI were associated with this outcome. Multivariate analysis demonstrated that high levels of PGRN [HR 2.50 (95%CI 2.47–2.52)] or TNFR1 [HR 5.38 (95%CI 5.26–5.50)] were associated with this outcome after adjusting for relevant covariates. The high levels of PGRN as well as TNFR1 were associated with a risk of primary renal outcome in patients with type 2 diabetes after adjusting for established risk factors. Frontiers Media S.A. 2022-04-01 /pmc/articles/PMC9012489/ /pubmed/35432201 http://dx.doi.org/10.3389/fendo.2022.849457 Text en Copyright © 2022 Murakoshi, Gohda, Sakuma, Shibata, Adachi, Kishida, Ichikawa, Koshida, Kamei and Suzuki https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Endocrinology Murakoshi, Maki Gohda, Tomohito Sakuma, Hiroko Shibata, Terumi Adachi, Eri Kishida, Chiaki Ichikawa, Saki Koshida, Takeo Kamei, Nozomu Suzuki, Yusuke Progranulin and Its Receptor Predict Kidney Function Decline in Patients With Type 2 Diabetes |
title | Progranulin and Its Receptor Predict Kidney Function Decline in Patients With Type 2 Diabetes |
title_full | Progranulin and Its Receptor Predict Kidney Function Decline in Patients With Type 2 Diabetes |
title_fullStr | Progranulin and Its Receptor Predict Kidney Function Decline in Patients With Type 2 Diabetes |
title_full_unstemmed | Progranulin and Its Receptor Predict Kidney Function Decline in Patients With Type 2 Diabetes |
title_short | Progranulin and Its Receptor Predict Kidney Function Decline in Patients With Type 2 Diabetes |
title_sort | progranulin and its receptor predict kidney function decline in patients with type 2 diabetes |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9012489/ https://www.ncbi.nlm.nih.gov/pubmed/35432201 http://dx.doi.org/10.3389/fendo.2022.849457 |
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