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The Level of Urine Dipstick Proteinuria and Its Relation to the Risk of Incident Cholelithiasis

BACKGROUND: Previous studies have suggested the potential association between renal diseases and gallstone. The extent of proteinuria is recognized as a marker for the severity of chronic kidney disease. However, little data is available to identify the risk of incident gallstone according to the le...

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Autores principales: Park, Sung Keun, Jung, Ju Young, Oh, Chang-Mo, Kim, Min-Ho, Ha, Eunhee, Lee, Dong-Young, Kim, Jung-Wook, Kang, Hee Yong, Ryoo, Jae-Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japan Epidemiological Association 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7738639/
https://www.ncbi.nlm.nih.gov/pubmed/31956168
http://dx.doi.org/10.2188/jea.JE20190223
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author Park, Sung Keun
Jung, Ju Young
Oh, Chang-Mo
Kim, Min-Ho
Ha, Eunhee
Lee, Dong-Young
Kim, Jung-Wook
Kang, Hee Yong
Ryoo, Jae-Hong
author_facet Park, Sung Keun
Jung, Ju Young
Oh, Chang-Mo
Kim, Min-Ho
Ha, Eunhee
Lee, Dong-Young
Kim, Jung-Wook
Kang, Hee Yong
Ryoo, Jae-Hong
author_sort Park, Sung Keun
collection PubMed
description BACKGROUND: Previous studies have suggested the potential association between renal diseases and gallstone. The extent of proteinuria is recognized as a marker for the severity of chronic kidney disease. However, little data is available to identify the risk of incident gallstone according to the level of proteinuria. METHODS: Using a data of 207,356 Koreans registered in National Health Insurance Database, we evaluated the risk of gallstone according to the levels of urine dipstick proteinuria through an average follow-up of 4.36 years. Study subjects were divided into 3 groups by urine dipstick proteinuria (negative: 0, mild: 1+ and heavy: 2+ or greater). Multivariate Cox-proportional hazard model was used to assess the adjusted hazard ratios (HRs) and 95% confidence intervals (CIs) for incident cholelithiasis according to urine dipstick proteinuria. RESULTS: The group with higher urine dipstick proteinuria had worse metabolic, renal, and hepatic profiles than those without proteinuria, which were similarly observed in the group with incident cholelithiasis. The heavy proteinuria group had the greatest incidence of cholelithiasis (2.39%), followed by mild (1.54%) and negative proteinuria groups (1.39%). Analysis for multivariate Cox-proportional hazard model indicated that the heavy proteinuria group had higher risk of cholelithiasis than other groups (negative: reference, mild proteinuria: HR 0.97 [95% CI, 0.74–1.26], and heavy proteinuria: HR 1.46 [95% CI, 1.09–1.96]). CONCLUSION: Urine dipstick proteinuria of 2+ or greater was significantly associated with increased risk for incident gallstone.
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spelling pubmed-77386392021-01-05 The Level of Urine Dipstick Proteinuria and Its Relation to the Risk of Incident Cholelithiasis Park, Sung Keun Jung, Ju Young Oh, Chang-Mo Kim, Min-Ho Ha, Eunhee Lee, Dong-Young Kim, Jung-Wook Kang, Hee Yong Ryoo, Jae-Hong J Epidemiol Original Article BACKGROUND: Previous studies have suggested the potential association between renal diseases and gallstone. The extent of proteinuria is recognized as a marker for the severity of chronic kidney disease. However, little data is available to identify the risk of incident gallstone according to the level of proteinuria. METHODS: Using a data of 207,356 Koreans registered in National Health Insurance Database, we evaluated the risk of gallstone according to the levels of urine dipstick proteinuria through an average follow-up of 4.36 years. Study subjects were divided into 3 groups by urine dipstick proteinuria (negative: 0, mild: 1+ and heavy: 2+ or greater). Multivariate Cox-proportional hazard model was used to assess the adjusted hazard ratios (HRs) and 95% confidence intervals (CIs) for incident cholelithiasis according to urine dipstick proteinuria. RESULTS: The group with higher urine dipstick proteinuria had worse metabolic, renal, and hepatic profiles than those without proteinuria, which were similarly observed in the group with incident cholelithiasis. The heavy proteinuria group had the greatest incidence of cholelithiasis (2.39%), followed by mild (1.54%) and negative proteinuria groups (1.39%). Analysis for multivariate Cox-proportional hazard model indicated that the heavy proteinuria group had higher risk of cholelithiasis than other groups (negative: reference, mild proteinuria: HR 0.97 [95% CI, 0.74–1.26], and heavy proteinuria: HR 1.46 [95% CI, 1.09–1.96]). CONCLUSION: Urine dipstick proteinuria of 2+ or greater was significantly associated with increased risk for incident gallstone. Japan Epidemiological Association 2021-01-05 /pmc/articles/PMC7738639/ /pubmed/31956168 http://dx.doi.org/10.2188/jea.JE20190223 Text en © 2020 Sung Keun Park et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Original Article
Park, Sung Keun
Jung, Ju Young
Oh, Chang-Mo
Kim, Min-Ho
Ha, Eunhee
Lee, Dong-Young
Kim, Jung-Wook
Kang, Hee Yong
Ryoo, Jae-Hong
The Level of Urine Dipstick Proteinuria and Its Relation to the Risk of Incident Cholelithiasis
title The Level of Urine Dipstick Proteinuria and Its Relation to the Risk of Incident Cholelithiasis
title_full The Level of Urine Dipstick Proteinuria and Its Relation to the Risk of Incident Cholelithiasis
title_fullStr The Level of Urine Dipstick Proteinuria and Its Relation to the Risk of Incident Cholelithiasis
title_full_unstemmed The Level of Urine Dipstick Proteinuria and Its Relation to the Risk of Incident Cholelithiasis
title_short The Level of Urine Dipstick Proteinuria and Its Relation to the Risk of Incident Cholelithiasis
title_sort level of urine dipstick proteinuria and its relation to the risk of incident cholelithiasis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7738639/
https://www.ncbi.nlm.nih.gov/pubmed/31956168
http://dx.doi.org/10.2188/jea.JE20190223
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