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Decreased Serum Osteocalcin is an Independent Risk Factor for Metabolic Dysfunction-Associated Fatty Liver Disease in Type 2 Diabetes
Purpose: The association between serum osteocalcin (OCN) levels and metabolic dysfunction-associated fatty liver disease (MAFLD) is still controversial. Moreover, few studies have explored their relationship in type 2 diabetes mellitus (T2DM) patients so far. The present study aimed to investigate t...
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Published in: | Diabetes, metabolic syndrome and obesity metabolic syndrome and obesity, 2022-01, Vol.15, p.3717-3728 |
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description | Purpose: The association between serum osteocalcin (OCN) levels and metabolic dysfunction-associated fatty liver disease (MAFLD) is still controversial. Moreover, few studies have explored their relationship in type 2 diabetes mellitus (T2DM) patients so far. The present study aimed to investigate the association of serum OCN levels with MAFLD in Chinese T2DM patients. Methods: This cross-sectional, real-world study included 1889 Chinese T2DM inpatients. MAFLD was diagnosed by abdominal ultrasonography. Participants were divided into four groups according to serum OCN quartiles, among which the clinical characteristics were compared. The association of serum OCN levels with the presence of MAFLD was also analyzed in subjects. Results: After controlling for sex, age, and diabetes duration, the prevalence of MAFLD significantly decreased across the serum OCN quartiles (55.3%, 52.0%, 48.6%, and 42.1% for the first, second, third, and fourth quartiles, respectively, P < 0.001 for trend). A fully adjusted multiple logistic regression analysis showed that serum OCN levels were independently and negatively associated with the presence of MAFLD in T2DM patients (odds ratio, 0.832; 95% confidence interval, 0.719-0.962; P = 0.013). Furthermore, there were significant decreases in HOMA-IR (P = 0.001 for trend) and C-reactive protein (P < 0.001 for trend) levels across the serum OCN quartiles after controlling for sex, age, and diabetes duration. Conclusion: Serum OCN levels were independently and negatively associated with the presence of MAFLD in Chinese T2DM patients, partially due to the improvement of insulin resistance and inflammation mediated by OCN. Serum OCN may be used as a biomarker to assess the risk of MAFLD in T2DM patients. Keywords: diabetes mellitus, type 2, metabolic dysfunction-associated fatty liver disease, osteocalcin, insulin resistance, inflammation |
doi_str_mv | 10.2147/DMSO.S389794 |
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fullrecord | <record><control><sourceid>gale_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_cd5ef675dd45434ab1aa2e09774208f7</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A730419675</galeid><doaj_id>oai_doaj_org_article_cd5ef675dd45434ab1aa2e09774208f7</doaj_id><sourcerecordid>A730419675</sourcerecordid><originalsourceid>FETCH-LOGICAL-c553t-dabaa9362ba74549e144af869f28ae27e04760420f2032871692c4bb5f17d0b93</originalsourceid><addsrcrecordid>eNptklGr0zAUgIsoeLneN39AQBAf3EzStGlfhMud08EuA3d9DqfpyZbZNTNJL-wH-L9N3dA7saFNOf3yHc7pybLXjE45E_LD7H69mq7zqpa1eJZdMSariaRUPn_y_jK7CWFHx0tSwflV9nOG2iMEbMka_bAnqxDRaei07YkNBHqy6Fs8YHr0kXy14TuZg47OE5Pue4zQuM5qMjsGM_Q6WtdPbkNw2kJM0jnEeCRL-4iezGwYM5FkfjgekPAUgQYjhlfZCwNdwJvzfp19m396uPsyWa4-L-5ulxNdFHmctNAA1HnJG5CiEDUyIcBUZW14BcglUiHLVBc1nOa8kqysuRZNUxgmW9rU-XW2OHlbBzt18HYP_qgcWPU74PxGgY9Wd6h0W6ApZdG2KVMuoGEAHGktZfJXRibXx5PrMDR7bHVqj4fuQnr5pbdbtXGPqpas5lWZBO_OAu9-DBii2tugseugRzcExaWQPKXLR_TNP-jODb5PrUpUUbBEMfmX2kAqwPbGpbx6lKpbmVPB6lRPoqb_odJqcW-169HYFL848PbJgS1CF7fBdcP4q8Ml-P4Eau9C8Gj-NINRNc6oGmdUnWc0_wVlTdeU</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2755177417</pqid></control><display><type>article</type><title>Decreased Serum Osteocalcin is an Independent Risk Factor for Metabolic Dysfunction-Associated Fatty Liver Disease in Type 2 Diabetes</title><source>Open Access: PubMed Central</source><source>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</source><source>Taylor & Francis (Open access)</source><creator>Wang, Yu-Jie ; Jin, Chun-Hua ; Ke, Jiang-Feng ; Wang, Jun-Wei ; Ma, Yi-Lin ; Lu, Jun-Xi ; Li, Mei-Fang ; Li, Lian-Xi</creator><creatorcontrib>Wang, Yu-Jie ; Jin, Chun-Hua ; Ke, Jiang-Feng ; Wang, Jun-Wei ; Ma, Yi-Lin ; Lu, Jun-Xi ; Li, Mei-Fang ; Li, Lian-Xi</creatorcontrib><description>Purpose: The association between serum osteocalcin (OCN) levels and metabolic dysfunction-associated fatty liver disease (MAFLD) is still controversial. Moreover, few studies have explored their relationship in type 2 diabetes mellitus (T2DM) patients so far. The present study aimed to investigate the association of serum OCN levels with MAFLD in Chinese T2DM patients. Methods: This cross-sectional, real-world study included 1889 Chinese T2DM inpatients. MAFLD was diagnosed by abdominal ultrasonography. Participants were divided into four groups according to serum OCN quartiles, among which the clinical characteristics were compared. The association of serum OCN levels with the presence of MAFLD was also analyzed in subjects. Results: After controlling for sex, age, and diabetes duration, the prevalence of MAFLD significantly decreased across the serum OCN quartiles (55.3%, 52.0%, 48.6%, and 42.1% for the first, second, third, and fourth quartiles, respectively, P < 0.001 for trend). A fully adjusted multiple logistic regression analysis showed that serum OCN levels were independently and negatively associated with the presence of MAFLD in T2DM patients (odds ratio, 0.832; 95% confidence interval, 0.719-0.962; P = 0.013). Furthermore, there were significant decreases in HOMA-IR (P = 0.001 for trend) and C-reactive protein (P < 0.001 for trend) levels across the serum OCN quartiles after controlling for sex, age, and diabetes duration. Conclusion: Serum OCN levels were independently and negatively associated with the presence of MAFLD in Chinese T2DM patients, partially due to the improvement of insulin resistance and inflammation mediated by OCN. Serum OCN may be used as a biomarker to assess the risk of MAFLD in T2DM patients. Keywords: diabetes mellitus, type 2, metabolic dysfunction-associated fatty liver disease, osteocalcin, insulin resistance, inflammation</description><identifier>ISSN: 1178-7007</identifier><identifier>EISSN: 1178-7007</identifier><identifier>DOI: 10.2147/DMSO.S389794</identifier><language>eng</language><publisher>Macclesfield: Dove Medical Press Limited</publisher><subject>Abdomen ; Age ; Blood pressure ; Body mass index ; C-reactive protein ; Cholesterol ; Comparative analysis ; Diabetes ; diabetes mellitus ; Fatty liver ; Glucose ; High density lipoprotein ; Hypertension ; inflammation ; Insulin resistance ; Laboratories ; Lipoproteins ; Liver diseases ; Medical colleges ; Medical research ; Medicine, Experimental ; metabolic dysfunction-associated fatty liver disease ; Metabolic syndrome ; Obesity ; Original Research ; osteocalcin ; Peptides ; Risk factors ; type 2 ; Type 2 diabetes ; Ultrasonic imaging ; Ultrasound imaging ; Variance analysis ; Womens health</subject><ispartof>Diabetes, metabolic syndrome and obesity, 2022-01, Vol.15, p.3717-3728</ispartof><rights>COPYRIGHT 2022 Dove Medical Press Limited</rights><rights>2022. This work is licensed under https://creativecommons.org/licenses/by-nc/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2022 Wang et al. 2022 Wang et al.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c553t-dabaa9362ba74549e144af869f28ae27e04760420f2032871692c4bb5f17d0b93</citedby><cites>FETCH-LOGICAL-c553t-dabaa9362ba74549e144af869f28ae27e04760420f2032871692c4bb5f17d0b93</cites><orcidid>0000-0001-6073-4901 ; 0000-0003-0937-4300</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2755177417/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2755177417?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids></links><search><creatorcontrib>Wang, Yu-Jie</creatorcontrib><creatorcontrib>Jin, Chun-Hua</creatorcontrib><creatorcontrib>Ke, Jiang-Feng</creatorcontrib><creatorcontrib>Wang, Jun-Wei</creatorcontrib><creatorcontrib>Ma, Yi-Lin</creatorcontrib><creatorcontrib>Lu, Jun-Xi</creatorcontrib><creatorcontrib>Li, Mei-Fang</creatorcontrib><creatorcontrib>Li, Lian-Xi</creatorcontrib><title>Decreased Serum Osteocalcin is an Independent Risk Factor for Metabolic Dysfunction-Associated Fatty Liver Disease in Type 2 Diabetes</title><title>Diabetes, metabolic syndrome and obesity</title><description>Purpose: The association between serum osteocalcin (OCN) levels and metabolic dysfunction-associated fatty liver disease (MAFLD) is still controversial. Moreover, few studies have explored their relationship in type 2 diabetes mellitus (T2DM) patients so far. The present study aimed to investigate the association of serum OCN levels with MAFLD in Chinese T2DM patients. Methods: This cross-sectional, real-world study included 1889 Chinese T2DM inpatients. MAFLD was diagnosed by abdominal ultrasonography. Participants were divided into four groups according to serum OCN quartiles, among which the clinical characteristics were compared. The association of serum OCN levels with the presence of MAFLD was also analyzed in subjects. Results: After controlling for sex, age, and diabetes duration, the prevalence of MAFLD significantly decreased across the serum OCN quartiles (55.3%, 52.0%, 48.6%, and 42.1% for the first, second, third, and fourth quartiles, respectively, P < 0.001 for trend). A fully adjusted multiple logistic regression analysis showed that serum OCN levels were independently and negatively associated with the presence of MAFLD in T2DM patients (odds ratio, 0.832; 95% confidence interval, 0.719-0.962; P = 0.013). Furthermore, there were significant decreases in HOMA-IR (P = 0.001 for trend) and C-reactive protein (P < 0.001 for trend) levels across the serum OCN quartiles after controlling for sex, age, and diabetes duration. Conclusion: Serum OCN levels were independently and negatively associated with the presence of MAFLD in Chinese T2DM patients, partially due to the improvement of insulin resistance and inflammation mediated by OCN. Serum OCN may be used as a biomarker to assess the risk of MAFLD in T2DM patients. Keywords: diabetes mellitus, type 2, metabolic dysfunction-associated fatty liver disease, osteocalcin, insulin resistance, inflammation</description><subject>Abdomen</subject><subject>Age</subject><subject>Blood pressure</subject><subject>Body mass index</subject><subject>C-reactive protein</subject><subject>Cholesterol</subject><subject>Comparative analysis</subject><subject>Diabetes</subject><subject>diabetes mellitus</subject><subject>Fatty liver</subject><subject>Glucose</subject><subject>High density lipoprotein</subject><subject>Hypertension</subject><subject>inflammation</subject><subject>Insulin resistance</subject><subject>Laboratories</subject><subject>Lipoproteins</subject><subject>Liver diseases</subject><subject>Medical colleges</subject><subject>Medical research</subject><subject>Medicine, Experimental</subject><subject>metabolic dysfunction-associated fatty liver disease</subject><subject>Metabolic syndrome</subject><subject>Obesity</subject><subject>Original Research</subject><subject>osteocalcin</subject><subject>Peptides</subject><subject>Risk factors</subject><subject>type 2</subject><subject>Type 2 diabetes</subject><subject>Ultrasonic imaging</subject><subject>Ultrasound imaging</subject><subject>Variance analysis</subject><subject>Womens health</subject><issn>1178-7007</issn><issn>1178-7007</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptklGr0zAUgIsoeLneN39AQBAf3EzStGlfhMud08EuA3d9DqfpyZbZNTNJL-wH-L9N3dA7saFNOf3yHc7pybLXjE45E_LD7H69mq7zqpa1eJZdMSariaRUPn_y_jK7CWFHx0tSwflV9nOG2iMEbMka_bAnqxDRaei07YkNBHqy6Fs8YHr0kXy14TuZg47OE5Pue4zQuM5qMjsGM_Q6WtdPbkNw2kJM0jnEeCRL-4iezGwYM5FkfjgekPAUgQYjhlfZCwNdwJvzfp19m396uPsyWa4-L-5ulxNdFHmctNAA1HnJG5CiEDUyIcBUZW14BcglUiHLVBc1nOa8kqysuRZNUxgmW9rU-XW2OHlbBzt18HYP_qgcWPU74PxGgY9Wd6h0W6ApZdG2KVMuoGEAHGktZfJXRibXx5PrMDR7bHVqj4fuQnr5pbdbtXGPqpas5lWZBO_OAu9-DBii2tugseugRzcExaWQPKXLR_TNP-jODb5PrUpUUbBEMfmX2kAqwPbGpbx6lKpbmVPB6lRPoqb_odJqcW-169HYFL848PbJgS1CF7fBdcP4q8Ml-P4Eau9C8Gj-NINRNc6oGmdUnWc0_wVlTdeU</recordid><startdate>20220101</startdate><enddate>20220101</enddate><creator>Wang, Yu-Jie</creator><creator>Jin, Chun-Hua</creator><creator>Ke, Jiang-Feng</creator><creator>Wang, Jun-Wei</creator><creator>Ma, Yi-Lin</creator><creator>Lu, Jun-Xi</creator><creator>Li, Mei-Fang</creator><creator>Li, Lian-Xi</creator><general>Dove Medical Press Limited</general><general>Taylor & Francis Ltd</general><general>Dove</general><general>Dove Medical Press</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7XB</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</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>GNUQQ</scope><scope>GUQSH</scope><scope>KB0</scope><scope>M2O</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-6073-4901</orcidid><orcidid>https://orcid.org/0000-0003-0937-4300</orcidid></search><sort><creationdate>20220101</creationdate><title>Decreased Serum Osteocalcin is an Independent Risk Factor for Metabolic Dysfunction-Associated Fatty Liver Disease in Type 2 Diabetes</title><author>Wang, Yu-Jie ; Jin, Chun-Hua ; Ke, Jiang-Feng ; Wang, Jun-Wei ; Ma, Yi-Lin ; Lu, Jun-Xi ; Li, Mei-Fang ; Li, Lian-Xi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c553t-dabaa9362ba74549e144af869f28ae27e04760420f2032871692c4bb5f17d0b93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Abdomen</topic><topic>Age</topic><topic>Blood pressure</topic><topic>Body mass index</topic><topic>C-reactive protein</topic><topic>Cholesterol</topic><topic>Comparative analysis</topic><topic>Diabetes</topic><topic>diabetes mellitus</topic><topic>Fatty liver</topic><topic>Glucose</topic><topic>High density lipoprotein</topic><topic>Hypertension</topic><topic>inflammation</topic><topic>Insulin resistance</topic><topic>Laboratories</topic><topic>Lipoproteins</topic><topic>Liver diseases</topic><topic>Medical colleges</topic><topic>Medical research</topic><topic>Medicine, Experimental</topic><topic>metabolic dysfunction-associated fatty liver disease</topic><topic>Metabolic syndrome</topic><topic>Obesity</topic><topic>Original Research</topic><topic>osteocalcin</topic><topic>Peptides</topic><topic>Risk factors</topic><topic>type 2</topic><topic>Type 2 diabetes</topic><topic>Ultrasonic imaging</topic><topic>Ultrasound imaging</topic><topic>Variance analysis</topic><topic>Womens health</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Yu-Jie</creatorcontrib><creatorcontrib>Jin, Chun-Hua</creatorcontrib><creatorcontrib>Ke, Jiang-Feng</creatorcontrib><creatorcontrib>Wang, Jun-Wei</creatorcontrib><creatorcontrib>Ma, Yi-Lin</creatorcontrib><creatorcontrib>Lu, Jun-Xi</creatorcontrib><creatorcontrib>Li, Mei-Fang</creatorcontrib><creatorcontrib>Li, Lian-Xi</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Nursing and Allied Health Journals</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: 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 Central Student</collection><collection>Research Library Prep</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Open Access: DOAJ - Directory of Open Access Journals</collection><jtitle>Diabetes, metabolic syndrome and obesity</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Yu-Jie</au><au>Jin, Chun-Hua</au><au>Ke, Jiang-Feng</au><au>Wang, Jun-Wei</au><au>Ma, Yi-Lin</au><au>Lu, Jun-Xi</au><au>Li, Mei-Fang</au><au>Li, Lian-Xi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Decreased Serum Osteocalcin is an Independent Risk Factor for Metabolic Dysfunction-Associated Fatty Liver Disease in Type 2 Diabetes</atitle><jtitle>Diabetes, metabolic syndrome and obesity</jtitle><date>2022-01-01</date><risdate>2022</risdate><volume>15</volume><spage>3717</spage><epage>3728</epage><pages>3717-3728</pages><issn>1178-7007</issn><eissn>1178-7007</eissn><abstract>Purpose: The association between serum osteocalcin (OCN) levels and metabolic dysfunction-associated fatty liver disease (MAFLD) is still controversial. Moreover, few studies have explored their relationship in type 2 diabetes mellitus (T2DM) patients so far. The present study aimed to investigate the association of serum OCN levels with MAFLD in Chinese T2DM patients. Methods: This cross-sectional, real-world study included 1889 Chinese T2DM inpatients. MAFLD was diagnosed by abdominal ultrasonography. Participants were divided into four groups according to serum OCN quartiles, among which the clinical characteristics were compared. The association of serum OCN levels with the presence of MAFLD was also analyzed in subjects. Results: After controlling for sex, age, and diabetes duration, the prevalence of MAFLD significantly decreased across the serum OCN quartiles (55.3%, 52.0%, 48.6%, and 42.1% for the first, second, third, and fourth quartiles, respectively, P < 0.001 for trend). A fully adjusted multiple logistic regression analysis showed that serum OCN levels were independently and negatively associated with the presence of MAFLD in T2DM patients (odds ratio, 0.832; 95% confidence interval, 0.719-0.962; P = 0.013). Furthermore, there were significant decreases in HOMA-IR (P = 0.001 for trend) and C-reactive protein (P < 0.001 for trend) levels across the serum OCN quartiles after controlling for sex, age, and diabetes duration. Conclusion: Serum OCN levels were independently and negatively associated with the presence of MAFLD in Chinese T2DM patients, partially due to the improvement of insulin resistance and inflammation mediated by OCN. Serum OCN may be used as a biomarker to assess the risk of MAFLD in T2DM patients. Keywords: diabetes mellitus, type 2, metabolic dysfunction-associated fatty liver disease, osteocalcin, insulin resistance, inflammation</abstract><cop>Macclesfield</cop><pub>Dove Medical Press Limited</pub><doi>10.2147/DMSO.S389794</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0001-6073-4901</orcidid><orcidid>https://orcid.org/0000-0003-0937-4300</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Abdomen Age Blood pressure Body mass index C-reactive protein Cholesterol Comparative analysis Diabetes diabetes mellitus Fatty liver Glucose High density lipoprotein Hypertension inflammation Insulin resistance Laboratories Lipoproteins Liver diseases Medical colleges Medical research Medicine, Experimental metabolic dysfunction-associated fatty liver disease Metabolic syndrome Obesity Original Research osteocalcin Peptides Risk factors type 2 Type 2 diabetes Ultrasonic imaging Ultrasound imaging Variance analysis Womens health |
title | Decreased Serum Osteocalcin is an Independent Risk Factor for Metabolic Dysfunction-Associated Fatty Liver Disease in Type 2 Diabetes |
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