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The impact of microalbuminuria on overactive bladders: Results from a community‐based four‐year longitudinal study in Japan

Aims To investigate the longitudinal association of microalbuminuria with overactive bladder (OAB). Methods This longitudinal study investigated 561 participants of the Iwaki Health Promotion Project in both 2015 and 2019 in Japan. Microalbuminuria and OAB symptoms were assessed using the urine albu...

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Published in:Neurourology and urodynamics 2020-06, Vol.39 (5), p.1567-1575
Main Authors: Okamoto, Teppei, Hatakeyama, Shingo, Ando, Masataka, Songee, Jung, Imai, Atsushi, Hamano, Itsuto, Fujita, Naoki, Okamoto, Akiko, Yamamoto, Hayato, Yoneyama, Tohru, Yoneyama, Takahiro, Hashimoto, Yasuhiro, Ohyama, Chikara
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container_end_page 1575
container_issue 5
container_start_page 1567
container_title Neurourology and urodynamics
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creator Okamoto, Teppei
Hatakeyama, Shingo
Ando, Masataka
Songee, Jung
Imai, Atsushi
Hamano, Itsuto
Fujita, Naoki
Okamoto, Akiko
Yamamoto, Hayato
Yoneyama, Tohru
Yoneyama, Takahiro
Hashimoto, Yasuhiro
Ohyama, Chikara
description Aims To investigate the longitudinal association of microalbuminuria with overactive bladder (OAB). Methods This longitudinal study investigated 561 participants of the Iwaki Health Promotion Project in both 2015 and 2019 in Japan. Microalbuminuria and OAB symptoms were assessed using the urine albuminuria creatinine ratio (ACR) and the overactive bladder symptom score (OABSS), respectively. Urine ACR was defined as high if ≥9.3 mg/gCr. Differences in OABSS between 2015 and 2019 were evaluated as ∆OABSS. Participants were divided into two groups according to ΔOABSS: high (ΔOABSS > 1) and control (≤1). We used baseline data acquired in 2015, such as urine ACR, the Pittsburgh Sleep Quality Index (PSQI), and arterial stiffness expressed by brachial‐ankle pulse wave velocity (baPWV). Predictive factors of a ΔOABSS > 1 were assessed by multivariable logistic regression analysis. Results This study included 332 women and 229 men. Of those, 86 (34 males and 52 females) were classified into the ΔOABSS > 1 group. There were significant group differences in age, renal function, and hemoglobin A1c. Participants in the ΔOABSS > 1 had a higher prevalence of PSQI > 5, baPWV ≥ 1400 seconds/cm, and urine ACR ≥ 9.3 mg/gCr (49% vs 20%, P = .001) than those in the control group. Multivariable analysis revealed that PSQI > 5 (odds ratio [OR], 2.57; 95% confidence interval [CI], 1.15‐4.60; P = .002) and urine ACR ≥ 9.3 mg/gCr (OR, 1.93; 95% CI, 1.15‐3.23; P = .013) were independent risk factors for ΔOABSS > 1. Conclusions Microalbuminuria may be an independent risk indicator for OAB symptom exacerbation.
doi_str_mv 10.1002/nau.24405
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Methods This longitudinal study investigated 561 participants of the Iwaki Health Promotion Project in both 2015 and 2019 in Japan. Microalbuminuria and OAB symptoms were assessed using the urine albuminuria creatinine ratio (ACR) and the overactive bladder symptom score (OABSS), respectively. Urine ACR was defined as high if ≥9.3 mg/gCr. Differences in OABSS between 2015 and 2019 were evaluated as ∆OABSS. Participants were divided into two groups according to ΔOABSS: high (ΔOABSS &gt; 1) and control (≤1). We used baseline data acquired in 2015, such as urine ACR, the Pittsburgh Sleep Quality Index (PSQI), and arterial stiffness expressed by brachial‐ankle pulse wave velocity (baPWV). Predictive factors of a ΔOABSS &gt; 1 were assessed by multivariable logistic regression analysis. Results This study included 332 women and 229 men. Of those, 86 (34 males and 52 females) were classified into the ΔOABSS &gt; 1 group. There were significant group differences in age, renal function, and hemoglobin A1c. Participants in the ΔOABSS &gt; 1 had a higher prevalence of PSQI &gt; 5, baPWV ≥ 1400 seconds/cm, and urine ACR ≥ 9.3 mg/gCr (49% vs 20%, P = .001) than those in the control group. Multivariable analysis revealed that PSQI &gt; 5 (odds ratio [OR], 2.57; 95% confidence interval [CI], 1.15‐4.60; P = .002) and urine ACR ≥ 9.3 mg/gCr (OR, 1.93; 95% CI, 1.15‐3.23; P = .013) were independent risk factors for ΔOABSS &gt; 1. Conclusions Microalbuminuria may be an independent risk indicator for OAB symptom exacerbation.</description><identifier>ISSN: 0733-2467</identifier><identifier>EISSN: 1520-6777</identifier><identifier>DOI: 10.1002/nau.24405</identifier><identifier>PMID: 32460389</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Adult ; Aged ; Albuminuria - complications ; Albuminuria - physiopathology ; Albuminuria - urine ; Ankle ; Ankle Brachial Index ; arterial stiffness ; Brachial Artery - physiopathology ; Creatinine ; Creatinine - urine ; Female ; Hemoglobin ; Humans ; Japan ; Longitudinal Studies ; Male ; microalbuminuria ; Middle Aged ; overactive bladder ; Pulse Wave Analysis ; Renal function ; risk factor ; Risk Factors ; Sleep ; sleep disturbance ; Urinary Bladder, Overactive - complications ; Urinary Bladder, Overactive - physiopathology ; Urinary Bladder, Overactive - urine ; Urine ; Vascular Stiffness - physiology</subject><ispartof>Neurourology and urodynamics, 2020-06, Vol.39 (5), p.1567-1575</ispartof><rights>2020 Wiley Periodicals LLC</rights><rights>2020 Wiley Periodicals LLC.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4195-f6feb22211803cc8366b958c18ace333e20572867161650fb742b20858c9d2433</citedby><cites>FETCH-LOGICAL-c4195-f6feb22211803cc8366b958c18ace333e20572867161650fb742b20858c9d2433</cites><orcidid>0000-0002-3750-3811 ; 0000-0002-0026-4079</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32460389$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Okamoto, Teppei</creatorcontrib><creatorcontrib>Hatakeyama, Shingo</creatorcontrib><creatorcontrib>Ando, Masataka</creatorcontrib><creatorcontrib>Songee, Jung</creatorcontrib><creatorcontrib>Imai, Atsushi</creatorcontrib><creatorcontrib>Hamano, Itsuto</creatorcontrib><creatorcontrib>Fujita, Naoki</creatorcontrib><creatorcontrib>Okamoto, Akiko</creatorcontrib><creatorcontrib>Yamamoto, Hayato</creatorcontrib><creatorcontrib>Yoneyama, Tohru</creatorcontrib><creatorcontrib>Yoneyama, Takahiro</creatorcontrib><creatorcontrib>Hashimoto, Yasuhiro</creatorcontrib><creatorcontrib>Ohyama, Chikara</creatorcontrib><title>The impact of microalbuminuria on overactive bladders: Results from a community‐based four‐year longitudinal study in Japan</title><title>Neurourology and urodynamics</title><addtitle>Neurourol Urodyn</addtitle><description>Aims To investigate the longitudinal association of microalbuminuria with overactive bladder (OAB). Methods This longitudinal study investigated 561 participants of the Iwaki Health Promotion Project in both 2015 and 2019 in Japan. Microalbuminuria and OAB symptoms were assessed using the urine albuminuria creatinine ratio (ACR) and the overactive bladder symptom score (OABSS), respectively. Urine ACR was defined as high if ≥9.3 mg/gCr. Differences in OABSS between 2015 and 2019 were evaluated as ∆OABSS. Participants were divided into two groups according to ΔOABSS: high (ΔOABSS &gt; 1) and control (≤1). We used baseline data acquired in 2015, such as urine ACR, the Pittsburgh Sleep Quality Index (PSQI), and arterial stiffness expressed by brachial‐ankle pulse wave velocity (baPWV). Predictive factors of a ΔOABSS &gt; 1 were assessed by multivariable logistic regression analysis. Results This study included 332 women and 229 men. Of those, 86 (34 males and 52 females) were classified into the ΔOABSS &gt; 1 group. There were significant group differences in age, renal function, and hemoglobin A1c. Participants in the ΔOABSS &gt; 1 had a higher prevalence of PSQI &gt; 5, baPWV ≥ 1400 seconds/cm, and urine ACR ≥ 9.3 mg/gCr (49% vs 20%, P = .001) than those in the control group. Multivariable analysis revealed that PSQI &gt; 5 (odds ratio [OR], 2.57; 95% confidence interval [CI], 1.15‐4.60; P = .002) and urine ACR ≥ 9.3 mg/gCr (OR, 1.93; 95% CI, 1.15‐3.23; P = .013) were independent risk factors for ΔOABSS &gt; 1. Conclusions Microalbuminuria may be an independent risk indicator for OAB symptom exacerbation.</description><subject>Adult</subject><subject>Aged</subject><subject>Albuminuria - complications</subject><subject>Albuminuria - physiopathology</subject><subject>Albuminuria - urine</subject><subject>Ankle</subject><subject>Ankle Brachial Index</subject><subject>arterial stiffness</subject><subject>Brachial Artery - physiopathology</subject><subject>Creatinine</subject><subject>Creatinine - urine</subject><subject>Female</subject><subject>Hemoglobin</subject><subject>Humans</subject><subject>Japan</subject><subject>Longitudinal Studies</subject><subject>Male</subject><subject>microalbuminuria</subject><subject>Middle Aged</subject><subject>overactive bladder</subject><subject>Pulse Wave Analysis</subject><subject>Renal function</subject><subject>risk factor</subject><subject>Risk Factors</subject><subject>Sleep</subject><subject>sleep disturbance</subject><subject>Urinary Bladder, Overactive - complications</subject><subject>Urinary Bladder, Overactive - physiopathology</subject><subject>Urinary Bladder, Overactive - urine</subject><subject>Urine</subject><subject>Vascular Stiffness - physiology</subject><issn>0733-2467</issn><issn>1520-6777</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp10clu1TAYBWALgejlwoIXQJbYlEVaT4kddlVFGVSBhNp15Dh_wJWHix0XZVUegWfkSXB7CwskVp4-HTs5CD2n5IgSwo6DLkdMCNI-QBvaMtJ0UsqHaEMk5w0TnTxAT3K-IoQoLvrH6IDXTcJVv0E3F18BW7_TZsFxxt6aFLUbi7ehJKtxDDheQ6rH9hrw6PQ0Qcqv8WfIxS0Zzyl6rLGJ3pdgl_XXj5-jzjDhOZZUFyvohF0MX-xSJhu0w7lOVmwD_qB3OjxFj2btMjy7H7fo8uzNxem75vzT2_enJ-eNEbRvm7mbYWSMUaoIN0bxrhv7VhmqtAHOOTDSSqY6STvatWQepWAjI6qSfmKC8y063OfuUvxWIC-Dt9mAczpALHlggshWCVXtFr38h17Vb6lPv1WUt_XyO_Vqr-oPyznBPOyS9TqtAyXDbStDbWW4a6XaF_eJZfQw_ZV_aqjgeA--Wwfr_5OGjyeX-8jfvVCYVg</recordid><startdate>202006</startdate><enddate>202006</enddate><creator>Okamoto, Teppei</creator><creator>Hatakeyama, Shingo</creator><creator>Ando, Masataka</creator><creator>Songee, Jung</creator><creator>Imai, Atsushi</creator><creator>Hamano, Itsuto</creator><creator>Fujita, Naoki</creator><creator>Okamoto, Akiko</creator><creator>Yamamoto, Hayato</creator><creator>Yoneyama, Tohru</creator><creator>Yoneyama, Takahiro</creator><creator>Hashimoto, Yasuhiro</creator><creator>Ohyama, Chikara</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>7TK</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-3750-3811</orcidid><orcidid>https://orcid.org/0000-0002-0026-4079</orcidid></search><sort><creationdate>202006</creationdate><title>The impact of microalbuminuria on overactive bladders: Results from a community‐based four‐year longitudinal study in Japan</title><author>Okamoto, Teppei ; Hatakeyama, Shingo ; Ando, Masataka ; Songee, Jung ; Imai, Atsushi ; Hamano, Itsuto ; Fujita, Naoki ; Okamoto, Akiko ; Yamamoto, Hayato ; Yoneyama, Tohru ; Yoneyama, Takahiro ; Hashimoto, Yasuhiro ; Ohyama, Chikara</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4195-f6feb22211803cc8366b958c18ace333e20572867161650fb742b20858c9d2433</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Albuminuria - complications</topic><topic>Albuminuria - physiopathology</topic><topic>Albuminuria - urine</topic><topic>Ankle</topic><topic>Ankle Brachial Index</topic><topic>arterial stiffness</topic><topic>Brachial Artery - physiopathology</topic><topic>Creatinine</topic><topic>Creatinine - urine</topic><topic>Female</topic><topic>Hemoglobin</topic><topic>Humans</topic><topic>Japan</topic><topic>Longitudinal Studies</topic><topic>Male</topic><topic>microalbuminuria</topic><topic>Middle Aged</topic><topic>overactive bladder</topic><topic>Pulse Wave Analysis</topic><topic>Renal function</topic><topic>risk factor</topic><topic>Risk Factors</topic><topic>Sleep</topic><topic>sleep disturbance</topic><topic>Urinary Bladder, Overactive - complications</topic><topic>Urinary Bladder, Overactive - physiopathology</topic><topic>Urinary Bladder, Overactive - urine</topic><topic>Urine</topic><topic>Vascular Stiffness - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Okamoto, Teppei</creatorcontrib><creatorcontrib>Hatakeyama, Shingo</creatorcontrib><creatorcontrib>Ando, Masataka</creatorcontrib><creatorcontrib>Songee, Jung</creatorcontrib><creatorcontrib>Imai, Atsushi</creatorcontrib><creatorcontrib>Hamano, Itsuto</creatorcontrib><creatorcontrib>Fujita, Naoki</creatorcontrib><creatorcontrib>Okamoto, Akiko</creatorcontrib><creatorcontrib>Yamamoto, Hayato</creatorcontrib><creatorcontrib>Yoneyama, Tohru</creatorcontrib><creatorcontrib>Yoneyama, Takahiro</creatorcontrib><creatorcontrib>Hashimoto, Yasuhiro</creatorcontrib><creatorcontrib>Ohyama, Chikara</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Neurourology and urodynamics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Okamoto, Teppei</au><au>Hatakeyama, Shingo</au><au>Ando, Masataka</au><au>Songee, Jung</au><au>Imai, Atsushi</au><au>Hamano, Itsuto</au><au>Fujita, Naoki</au><au>Okamoto, Akiko</au><au>Yamamoto, Hayato</au><au>Yoneyama, Tohru</au><au>Yoneyama, Takahiro</au><au>Hashimoto, Yasuhiro</au><au>Ohyama, Chikara</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The impact of microalbuminuria on overactive bladders: Results from a community‐based four‐year longitudinal study in Japan</atitle><jtitle>Neurourology and urodynamics</jtitle><addtitle>Neurourol Urodyn</addtitle><date>2020-06</date><risdate>2020</risdate><volume>39</volume><issue>5</issue><spage>1567</spage><epage>1575</epage><pages>1567-1575</pages><issn>0733-2467</issn><eissn>1520-6777</eissn><abstract>Aims To investigate the longitudinal association of microalbuminuria with overactive bladder (OAB). Methods This longitudinal study investigated 561 participants of the Iwaki Health Promotion Project in both 2015 and 2019 in Japan. Microalbuminuria and OAB symptoms were assessed using the urine albuminuria creatinine ratio (ACR) and the overactive bladder symptom score (OABSS), respectively. Urine ACR was defined as high if ≥9.3 mg/gCr. Differences in OABSS between 2015 and 2019 were evaluated as ∆OABSS. Participants were divided into two groups according to ΔOABSS: high (ΔOABSS &gt; 1) and control (≤1). We used baseline data acquired in 2015, such as urine ACR, the Pittsburgh Sleep Quality Index (PSQI), and arterial stiffness expressed by brachial‐ankle pulse wave velocity (baPWV). Predictive factors of a ΔOABSS &gt; 1 were assessed by multivariable logistic regression analysis. Results This study included 332 women and 229 men. Of those, 86 (34 males and 52 females) were classified into the ΔOABSS &gt; 1 group. There were significant group differences in age, renal function, and hemoglobin A1c. Participants in the ΔOABSS &gt; 1 had a higher prevalence of PSQI &gt; 5, baPWV ≥ 1400 seconds/cm, and urine ACR ≥ 9.3 mg/gCr (49% vs 20%, P = .001) than those in the control group. Multivariable analysis revealed that PSQI &gt; 5 (odds ratio [OR], 2.57; 95% confidence interval [CI], 1.15‐4.60; P = .002) and urine ACR ≥ 9.3 mg/gCr (OR, 1.93; 95% CI, 1.15‐3.23; P = .013) were independent risk factors for ΔOABSS &gt; 1. Conclusions Microalbuminuria may be an independent risk indicator for OAB symptom exacerbation.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>32460389</pmid><doi>10.1002/nau.24405</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-3750-3811</orcidid><orcidid>https://orcid.org/0000-0002-0026-4079</orcidid></addata></record>
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1520-6777
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subjects Adult
Aged
Albuminuria - complications
Albuminuria - physiopathology
Albuminuria - urine
Ankle
Ankle Brachial Index
arterial stiffness
Brachial Artery - physiopathology
Creatinine
Creatinine - urine
Female
Hemoglobin
Humans
Japan
Longitudinal Studies
Male
microalbuminuria
Middle Aged
overactive bladder
Pulse Wave Analysis
Renal function
risk factor
Risk Factors
Sleep
sleep disturbance
Urinary Bladder, Overactive - complications
Urinary Bladder, Overactive - physiopathology
Urinary Bladder, Overactive - urine
Urine
Vascular Stiffness - physiology
title The impact of microalbuminuria on overactive bladders: Results from a community‐based four‐year longitudinal study in Japan
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