Prevalence and Risk Factors of MASLD and Liver Fibrosis amongst the Penitentiary Population in Catalonia: The PRISONAFLD Study
The prevalence of chronic non-communicable diseases, particularly metabolic syndrome (MetS), has increased among the prison population. Nevertheless, we have limited data on metabolic dysfunction-associated steatotic liver disease (MASLD), the hepatic manifestation of this syndrome. We aimed to inve...
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creator | Rivera-Esteban, Jesús Jiménez-Masip, Alba Muñoz-Martínez, Sergio Augustin, Salvador Guerrero, Rafael A Gabriel-Medina, Pablo Ferrer-Costa, Roser Rodríguez-Frías, Francisco Turu, Elisabet Marco, Andrés Pericàs, Juan M On Behalf Of The Prisonafld Study Group Collaborators |
description | The prevalence of chronic non-communicable diseases, particularly metabolic syndrome (MetS), has increased among the prison population. Nevertheless, we have limited data on metabolic dysfunction-associated steatotic liver disease (MASLD), the hepatic manifestation of this syndrome. We aimed to investigate the prevalence and risk factors of MASLD and MASLD-associated liver fibrosis in the penitentiary population in Catalonia, Spain.
A cross-sectional observational study involving eight penitentiary centers. Participants had at least one metabolic disorder and were at a closed-regimen penitentiary. Individuals with concomitant liver diseases and/or alcohol risk consumption were excluded. Significant fibrosis and MASLD were defined as liver stiffness ≥8 kPa and a controlled attenuation parameter ≥275 dB/m by vibration-controlled transient elastography (VCTE), respectively. After exclusions, metabolic inmates with VCTE were analyzed. Logistic regression analysis was performed to identify predictors of MASLD and MASLD-associated significant fibrosis.
Out of the 4338 inmates studied, 1290 (29.7%) had metabolic disorders, and 646 (14.9%) underwent VCTE. The mean age was 48.0 years (SD 12.1), and 89.5% were male. MASLD prevalence was 33.9%. Significant fibrosis and MASLD-associated significant fibrosis were found in 16.4% and 9.4% of inmates, respectively. In the multivariate analysis, T2D, waist circumference, MetS, and higher ALT values were identified as independent risk factors for MASLD and MASLD-associated significant fibrosis amongst the prison population.
Metabolic disorders including MASLD are highly prevalent among inmates. The prevalence of significant fibrosis seems notably higher than that of the general population, underscoring the need for targeted screening programs and therapeutic interventions in the incarcerated population. |
doi_str_mv | 10.3390/jcm12237276 |
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A cross-sectional observational study involving eight penitentiary centers. Participants had at least one metabolic disorder and were at a closed-regimen penitentiary. Individuals with concomitant liver diseases and/or alcohol risk consumption were excluded. Significant fibrosis and MASLD were defined as liver stiffness ≥8 kPa and a controlled attenuation parameter ≥275 dB/m by vibration-controlled transient elastography (VCTE), respectively. After exclusions, metabolic inmates with VCTE were analyzed. Logistic regression analysis was performed to identify predictors of MASLD and MASLD-associated significant fibrosis.
Out of the 4338 inmates studied, 1290 (29.7%) had metabolic disorders, and 646 (14.9%) underwent VCTE. The mean age was 48.0 years (SD 12.1), and 89.5% were male. MASLD prevalence was 33.9%. Significant fibrosis and MASLD-associated significant fibrosis were found in 16.4% and 9.4% of inmates, respectively. In the multivariate analysis, T2D, waist circumference, MetS, and higher ALT values were identified as independent risk factors for MASLD and MASLD-associated significant fibrosis amongst the prison population.
Metabolic disorders including MASLD are highly prevalent among inmates. The prevalence of significant fibrosis seems notably higher than that of the general population, underscoring the need for targeted screening programs and therapeutic interventions in the incarcerated population.</description><identifier>ISSN: 2077-0383</identifier><identifier>EISSN: 2077-0383</identifier><identifier>DOI: 10.3390/jcm12237276</identifier><identifier>PMID: 38068330</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Alcohol ; Blood pressure ; Chronic illnesses ; Clinical medicine ; Communicable diseases ; Demographic aspects ; Development and progression ; Diabetes ; Fatty liver ; Fibrosis ; Health aspects ; Hepatitis C ; Hypertension ; Infectious diseases ; Liver cirrhosis ; Liver diseases ; Medical research ; Medicine, Experimental ; Metabolic disorders ; Metabolic syndrome ; Obesity ; Population-based studies ; Prisoners ; Prisons ; Risk factors ; Statistics ; Substance abuse treatment ; Type 2 diabetes ; Womens health</subject><ispartof>Journal of clinical medicine, 2023-11, Vol.12 (23), p.7276</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><rights>2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c379t-9c01286a10bcb3864dab447ea5d582fc56493b476d9f7e505cfcc8a1bf63c7603</cites><orcidid>0000-0003-4357-8817 ; 0000-0003-0663-0575 ; 0000-0003-3079-6364 ; 0000-0002-9128-7013 ; 0000-0002-8925-3172</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38068330$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rivera-Esteban, Jesús</creatorcontrib><creatorcontrib>Jiménez-Masip, Alba</creatorcontrib><creatorcontrib>Muñoz-Martínez, Sergio</creatorcontrib><creatorcontrib>Augustin, Salvador</creatorcontrib><creatorcontrib>Guerrero, Rafael A</creatorcontrib><creatorcontrib>Gabriel-Medina, Pablo</creatorcontrib><creatorcontrib>Ferrer-Costa, Roser</creatorcontrib><creatorcontrib>Rodríguez-Frías, Francisco</creatorcontrib><creatorcontrib>Turu, Elisabet</creatorcontrib><creatorcontrib>Marco, Andrés</creatorcontrib><creatorcontrib>Pericàs, Juan M</creatorcontrib><creatorcontrib>On Behalf Of The Prisonafld Study Group Collaborators</creatorcontrib><creatorcontrib>on behalf of the PRISONAFLD Study Group Collaborators</creatorcontrib><title>Prevalence and Risk Factors of MASLD and Liver Fibrosis amongst the Penitentiary Population in Catalonia: The PRISONAFLD Study</title><title>Journal of clinical medicine</title><addtitle>J Clin Med</addtitle><description>The prevalence of chronic non-communicable diseases, particularly metabolic syndrome (MetS), has increased among the prison population. Nevertheless, we have limited data on metabolic dysfunction-associated steatotic liver disease (MASLD), the hepatic manifestation of this syndrome. We aimed to investigate the prevalence and risk factors of MASLD and MASLD-associated liver fibrosis in the penitentiary population in Catalonia, Spain.
A cross-sectional observational study involving eight penitentiary centers. Participants had at least one metabolic disorder and were at a closed-regimen penitentiary. Individuals with concomitant liver diseases and/or alcohol risk consumption were excluded. Significant fibrosis and MASLD were defined as liver stiffness ≥8 kPa and a controlled attenuation parameter ≥275 dB/m by vibration-controlled transient elastography (VCTE), respectively. After exclusions, metabolic inmates with VCTE were analyzed. Logistic regression analysis was performed to identify predictors of MASLD and MASLD-associated significant fibrosis.
Out of the 4338 inmates studied, 1290 (29.7%) had metabolic disorders, and 646 (14.9%) underwent VCTE. The mean age was 48.0 years (SD 12.1), and 89.5% were male. MASLD prevalence was 33.9%. Significant fibrosis and MASLD-associated significant fibrosis were found in 16.4% and 9.4% of inmates, respectively. In the multivariate analysis, T2D, waist circumference, MetS, and higher ALT values were identified as independent risk factors for MASLD and MASLD-associated significant fibrosis amongst the prison population.
Metabolic disorders including MASLD are highly prevalent among inmates. The prevalence of significant fibrosis seems notably higher than that of the general population, underscoring the need for targeted screening programs and therapeutic interventions in the incarcerated population.</description><subject>Alcohol</subject><subject>Blood pressure</subject><subject>Chronic illnesses</subject><subject>Clinical medicine</subject><subject>Communicable diseases</subject><subject>Demographic aspects</subject><subject>Development and progression</subject><subject>Diabetes</subject><subject>Fatty liver</subject><subject>Fibrosis</subject><subject>Health aspects</subject><subject>Hepatitis C</subject><subject>Hypertension</subject><subject>Infectious diseases</subject><subject>Liver cirrhosis</subject><subject>Liver diseases</subject><subject>Medical research</subject><subject>Medicine, Experimental</subject><subject>Metabolic disorders</subject><subject>Metabolic syndrome</subject><subject>Obesity</subject><subject>Population-based studies</subject><subject>Prisoners</subject><subject>Prisons</subject><subject>Risk factors</subject><subject>Statistics</subject><subject>Substance abuse treatment</subject><subject>Type 2 diabetes</subject><subject>Womens health</subject><issn>2077-0383</issn><issn>2077-0383</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNptkc1PHCEYxompqUY99W5IemnSrDIww0dvm23Xmmx149ozYRiwbGdgBcbES_922aqtNYUDBH7v8755HgDeVeiEEIFO13qoMCYMM7oD9jFibIIIJ29e3PfAUUprVBbnNa7YW7BHOKKcELQPfi2juVO98dpA5Tt45dJPOFc6h5hgsPDbdLX4_Ptn4e5MhHPXxpBcgmoI_iZlmH8YuDTeZeOzU_EeLsNm7FV2wUPn4Uxl1Qfv1Cd4vSWvzleXF9N50Vzlsbs_BLtW9ckcPZ0H4Pv8y_Xs62RxeXY-my4mmjCRJ0KjCnOqKtTqlnBad6qta2ZU0zUcW93QWpC2ZrQTlpkGNdpqzVXVWko0o4gcgA-PupsYbkeTshxc0qbvlTdhTBILhEVTHOMFff8KXYcx-jKdxFyIujSs6V_qppgnnbchR6W3onLKWMMFasi27cl_qLI7MzgdvLGuvP9T8PGxQBeXUzRWbqIbiq2yQnIbuHwReKGPn0Yd28F0f9jneMkDFcmi2g</recordid><startdate>20231124</startdate><enddate>20231124</enddate><creator>Rivera-Esteban, Jesús</creator><creator>Jiménez-Masip, Alba</creator><creator>Muñoz-Martínez, Sergio</creator><creator>Augustin, Salvador</creator><creator>Guerrero, Rafael A</creator><creator>Gabriel-Medina, Pablo</creator><creator>Ferrer-Costa, Roser</creator><creator>Rodríguez-Frías, Francisco</creator><creator>Turu, Elisabet</creator><creator>Marco, Andrés</creator><creator>Pericàs, Juan M</creator><creator>On Behalf Of The Prisonafld Study Group Collaborators</creator><general>MDPI AG</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-4357-8817</orcidid><orcidid>https://orcid.org/0000-0003-0663-0575</orcidid><orcidid>https://orcid.org/0000-0003-3079-6364</orcidid><orcidid>https://orcid.org/0000-0002-9128-7013</orcidid><orcidid>https://orcid.org/0000-0002-8925-3172</orcidid></search><sort><creationdate>20231124</creationdate><title>Prevalence and Risk Factors of MASLD and Liver Fibrosis amongst the Penitentiary Population in Catalonia: The PRISONAFLD Study</title><author>Rivera-Esteban, Jesús ; Jiménez-Masip, Alba ; Muñoz-Martínez, Sergio ; Augustin, Salvador ; Guerrero, Rafael A ; Gabriel-Medina, Pablo ; Ferrer-Costa, Roser ; Rodríguez-Frías, Francisco ; Turu, Elisabet ; Marco, Andrés ; Pericàs, Juan M ; On Behalf Of The Prisonafld Study Group Collaborators</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c379t-9c01286a10bcb3864dab447ea5d582fc56493b476d9f7e505cfcc8a1bf63c7603</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Alcohol</topic><topic>Blood pressure</topic><topic>Chronic illnesses</topic><topic>Clinical medicine</topic><topic>Communicable diseases</topic><topic>Demographic aspects</topic><topic>Development and progression</topic><topic>Diabetes</topic><topic>Fatty liver</topic><topic>Fibrosis</topic><topic>Health aspects</topic><topic>Hepatitis C</topic><topic>Hypertension</topic><topic>Infectious diseases</topic><topic>Liver cirrhosis</topic><topic>Liver diseases</topic><topic>Medical research</topic><topic>Medicine, Experimental</topic><topic>Metabolic disorders</topic><topic>Metabolic syndrome</topic><topic>Obesity</topic><topic>Population-based studies</topic><topic>Prisoners</topic><topic>Prisons</topic><topic>Risk factors</topic><topic>Statistics</topic><topic>Substance abuse treatment</topic><topic>Type 2 diabetes</topic><topic>Womens health</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rivera-Esteban, Jesús</creatorcontrib><creatorcontrib>Jiménez-Masip, Alba</creatorcontrib><creatorcontrib>Muñoz-Martínez, Sergio</creatorcontrib><creatorcontrib>Augustin, Salvador</creatorcontrib><creatorcontrib>Guerrero, Rafael A</creatorcontrib><creatorcontrib>Gabriel-Medina, Pablo</creatorcontrib><creatorcontrib>Ferrer-Costa, Roser</creatorcontrib><creatorcontrib>Rodríguez-Frías, Francisco</creatorcontrib><creatorcontrib>Turu, Elisabet</creatorcontrib><creatorcontrib>Marco, Andrés</creatorcontrib><creatorcontrib>Pericàs, Juan M</creatorcontrib><creatorcontrib>On Behalf Of The Prisonafld Study Group Collaborators</creatorcontrib><creatorcontrib>on behalf of the PRISONAFLD Study Group Collaborators</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Access via ProQuest (Open Access)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of clinical medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rivera-Esteban, Jesús</au><au>Jiménez-Masip, Alba</au><au>Muñoz-Martínez, Sergio</au><au>Augustin, Salvador</au><au>Guerrero, Rafael A</au><au>Gabriel-Medina, Pablo</au><au>Ferrer-Costa, Roser</au><au>Rodríguez-Frías, Francisco</au><au>Turu, Elisabet</au><au>Marco, Andrés</au><au>Pericàs, Juan M</au><au>On Behalf Of The Prisonafld Study Group Collaborators</au><aucorp>on behalf of the PRISONAFLD Study Group Collaborators</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prevalence and Risk Factors of MASLD and Liver Fibrosis amongst the Penitentiary Population in Catalonia: The PRISONAFLD Study</atitle><jtitle>Journal of clinical medicine</jtitle><addtitle>J Clin Med</addtitle><date>2023-11-24</date><risdate>2023</risdate><volume>12</volume><issue>23</issue><spage>7276</spage><pages>7276-</pages><issn>2077-0383</issn><eissn>2077-0383</eissn><abstract>The prevalence of chronic non-communicable diseases, particularly metabolic syndrome (MetS), has increased among the prison population. Nevertheless, we have limited data on metabolic dysfunction-associated steatotic liver disease (MASLD), the hepatic manifestation of this syndrome. We aimed to investigate the prevalence and risk factors of MASLD and MASLD-associated liver fibrosis in the penitentiary population in Catalonia, Spain.
A cross-sectional observational study involving eight penitentiary centers. Participants had at least one metabolic disorder and were at a closed-regimen penitentiary. Individuals with concomitant liver diseases and/or alcohol risk consumption were excluded. Significant fibrosis and MASLD were defined as liver stiffness ≥8 kPa and a controlled attenuation parameter ≥275 dB/m by vibration-controlled transient elastography (VCTE), respectively. After exclusions, metabolic inmates with VCTE were analyzed. Logistic regression analysis was performed to identify predictors of MASLD and MASLD-associated significant fibrosis.
Out of the 4338 inmates studied, 1290 (29.7%) had metabolic disorders, and 646 (14.9%) underwent VCTE. The mean age was 48.0 years (SD 12.1), and 89.5% were male. MASLD prevalence was 33.9%. Significant fibrosis and MASLD-associated significant fibrosis were found in 16.4% and 9.4% of inmates, respectively. In the multivariate analysis, T2D, waist circumference, MetS, and higher ALT values were identified as independent risk factors for MASLD and MASLD-associated significant fibrosis amongst the prison population.
Metabolic disorders including MASLD are highly prevalent among inmates. The prevalence of significant fibrosis seems notably higher than that of the general population, underscoring the need for targeted screening programs and therapeutic interventions in the incarcerated population.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>38068330</pmid><doi>10.3390/jcm12237276</doi><orcidid>https://orcid.org/0000-0003-4357-8817</orcidid><orcidid>https://orcid.org/0000-0003-0663-0575</orcidid><orcidid>https://orcid.org/0000-0003-3079-6364</orcidid><orcidid>https://orcid.org/0000-0002-9128-7013</orcidid><orcidid>https://orcid.org/0000-0002-8925-3172</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Alcohol Blood pressure Chronic illnesses Clinical medicine Communicable diseases Demographic aspects Development and progression Diabetes Fatty liver Fibrosis Health aspects Hepatitis C Hypertension Infectious diseases Liver cirrhosis Liver diseases Medical research Medicine, Experimental Metabolic disorders Metabolic syndrome Obesity Population-based studies Prisoners Prisons Risk factors Statistics Substance abuse treatment Type 2 diabetes Womens health |
title | Prevalence and Risk Factors of MASLD and Liver Fibrosis amongst the Penitentiary Population in Catalonia: The PRISONAFLD Study |
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