Serum L C3-II levels in type 2 diabetic patients with impaired renal functions
A total of 176 Turkish subjects were enrolled, of whom 26 were healthy, and 150 had type 2 diabetes mellitus. Under the light of American Diabetes Association criteria, we selected 150 patients and introduced them as type 2 DM. Patients were classified according to albumin urea ratio: 88 patients ha...
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description | A total of 176 Turkish subjects were enrolled, of whom 26 were healthy, and 150 had type 2 diabetes mellitus. Under the light of American Diabetes Association criteria, we selected 150 patients and introduced them as type 2 DM. Patients were classified according to albumin urea ratio: 88 patients had macroalbuminuria (ACR > 300 mg/g), 20 patients had microalbuminuria (ACR between 30 and 300 mg/g), and 42 had normoalbuminuria (ACR < 30 mg/g). According to eGFR values, T2DM patients were divided into six categories [standard to high (G1), slightly decreased (G2), slightly to moderately decreased (G3a), moderate to severely decreased (G3b), severely decreased (G4), and renal failure (G5)]. Proteinuria severity and eGFR stages were evaluated together and divided into three groups (Stage 1: Normoalbuminuria+G1/G2, Stage 2: Microalbuminuria+G3a/G3b, Stage 3: Macroalbuminuria+G5/G4).
There is no relationship between LC3-II levels and ACR in T2DM patients.
LC3-II has sufficient performance in the differential diagnosis of severe proteinuria.
[Display omitted]
•LC3-II levels were high in type 2 DM patients with DKD.•LC3-II elevation is higher in patients with severe proteinuria and advanced stage DKD.•The increase in LC3-II is accompanied by an increase in BCL-2 and TGF-β1.•The reason for the decrease in IL-1β in DKD may be inhibition due to the increase in LC3-II.•The increase in LC3-II can prevent tubular apoptosis by inhibiting the decrease in BCL-2.•Podocin levels are related to LC3-II in DKD patients.
This study was designed to evaluate serum LC3-II, BCL-2, IL-1β, TGF-β1, and podocin levels in.
type 2 diabetes (T2DM) patients with renal dysfunction.
176 Turkish subjects were enrolled, of whom 26 were healthy, and 150 had T2DM. Patients.
were classified according to albumin urea ratio: 88 patients had macroalbuminuria, 20.
patients had microalbuminuria, and 42 had normoalbuminuria. T2DM patients were also.
classified into three groups according to proteinuria and eGFR stages.
Increased serum LC3-II levels in patients with T2DM with increased urinary albumin.
extraction and impaired renal functions. There was a strong relationship between serum.
LC3-II levels and serum BCL-2, IL-1β, TGF-β1, and Podocin levels. The efficiency of LC3-
II as a diagnostic biomarker in the differential diagnosis of DM patients with.
macroproteinuria from DM patients with normoproteinuria was 75.4%.
It was thought that increased serum LC3-II levels in T2DM patients with impaired renal |
doi_str_mv | 10.1016/j.cyto.2024.156683 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_3073713940</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1043466624001868</els_id><sourcerecordid>3073713940</sourcerecordid><originalsourceid>FETCH-LOGICAL-c307t-4e2b8c8df1c6438575a52c127e4881570868185d5be1b88ff7ce4a8756b17a2c3</originalsourceid><addsrcrecordid>eNp90MtKAzEUBuAgiq3VF3AhWbqZmtskKbiR4qVQdKGuQyZzBlPmZpJR-vZOaXXp6pzFf_4DH0KXlMwpofJmM3fb1M0ZYWJOcyk1P0JTShYyI4Tx490ueCaklBN0FuOGELLgSp2iCdcLwRXXU_T8CmFo8BovebZa4Rq-oI7Ytzhte8AMl94WkLzDvU0e2hTxt08f2De99QFKHKC1Na6G1iXftfEcnVS2jnBxmDP0_nD_tnzK1i-Pq-XdOnOcqJQJYIV2uqyok4LrXOU2Z44yBUJrmiuipaY6L_MCaKF1VSkHwmqVy4Iqyxyfoet9bx-6zwFiMo2PDurattAN0YxfuKJ8IcgYZfuoC12MASrTB9_YsDWUmJ2j2Zido9k5mr3jeHR16B-KBsq_k1-4MXC7D4xc8OUhmOhGHwflyOKSKTv_X_8PRVuCUA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3073713940</pqid></control><display><type>article</type><title>Serum L C3-II levels in type 2 diabetic patients with impaired renal functions</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Ahmed Salıh Gezh, Shahab ; Deveci, Koksal ; Sivgin, Hakan ; Guzelgul, Figen</creator><creatorcontrib>Ahmed Salıh Gezh, Shahab ; Deveci, Koksal ; Sivgin, Hakan ; Guzelgul, Figen</creatorcontrib><description>A total of 176 Turkish subjects were enrolled, of whom 26 were healthy, and 150 had type 2 diabetes mellitus. Under the light of American Diabetes Association criteria, we selected 150 patients and introduced them as type 2 DM. Patients were classified according to albumin urea ratio: 88 patients had macroalbuminuria (ACR > 300 mg/g), 20 patients had microalbuminuria (ACR between 30 and 300 mg/g), and 42 had normoalbuminuria (ACR < 30 mg/g). According to eGFR values, T2DM patients were divided into six categories [standard to high (G1), slightly decreased (G2), slightly to moderately decreased (G3a), moderate to severely decreased (G3b), severely decreased (G4), and renal failure (G5)]. Proteinuria severity and eGFR stages were evaluated together and divided into three groups (Stage 1: Normoalbuminuria+G1/G2, Stage 2: Microalbuminuria+G3a/G3b, Stage 3: Macroalbuminuria+G5/G4).
There is no relationship between LC3-II levels and ACR in T2DM patients.
LC3-II has sufficient performance in the differential diagnosis of severe proteinuria.
[Display omitted]
•LC3-II levels were high in type 2 DM patients with DKD.•LC3-II elevation is higher in patients with severe proteinuria and advanced stage DKD.•The increase in LC3-II is accompanied by an increase in BCL-2 and TGF-β1.•The reason for the decrease in IL-1β in DKD may be inhibition due to the increase in LC3-II.•The increase in LC3-II can prevent tubular apoptosis by inhibiting the decrease in BCL-2.•Podocin levels are related to LC3-II in DKD patients.
This study was designed to evaluate serum LC3-II, BCL-2, IL-1β, TGF-β1, and podocin levels in.
type 2 diabetes (T2DM) patients with renal dysfunction.
176 Turkish subjects were enrolled, of whom 26 were healthy, and 150 had T2DM. Patients.
were classified according to albumin urea ratio: 88 patients had macroalbuminuria, 20.
patients had microalbuminuria, and 42 had normoalbuminuria. T2DM patients were also.
classified into three groups according to proteinuria and eGFR stages.
Increased serum LC3-II levels in patients with T2DM with increased urinary albumin.
extraction and impaired renal functions. There was a strong relationship between serum.
LC3-II levels and serum BCL-2, IL-1β, TGF-β1, and Podocin levels. The efficiency of LC3-
II as a diagnostic biomarker in the differential diagnosis of DM patients with.
macroproteinuria from DM patients with normoproteinuria was 75.4%.
It was thought that increased serum LC3-II levels in T2DM patients with impaired renal.
functions may cause renal podocyte damage. In these patients, serum LC3-II levels can be.
evaluated as a new biomarker to follow the development of renal damage.</description><identifier>ISSN: 1043-4666</identifier><identifier>ISSN: 1096-0023</identifier><identifier>EISSN: 1096-0023</identifier><identifier>DOI: 10.1016/j.cyto.2024.156683</identifier><identifier>PMID: 38943738</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Adult ; Aged ; Albuminuria - blood ; Autophagy ; BCL-2 ; Biomarkers - blood ; Diabetes Mellitus, Type 2 - blood ; Diabetes Mellitus, Type 2 - complications ; Diabetic Nephropathies - blood ; Diabetic Nephropathies - physiopathology ; DKD ; Female ; Glomerular Filtration Rate ; Humans ; Interleukin-1beta - blood ; Intracellular Signaling Peptides and Proteins ; Kidney - physiopathology ; LC3-II ; Male ; Membrane Proteins - blood ; Microtubule-Associated Proteins ; Middle Aged ; Podocin ; Proteinuria ; Proto-Oncogene Proteins c-bcl-2 - blood ; Transforming Growth Factor beta1 - blood</subject><ispartof>Cytokine (Philadelphia, Pa.), 2024-09, Vol.181, p.156683, Article 156683</ispartof><rights>2024</rights><rights>Copyright © 2024. Published by Elsevier Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c307t-4e2b8c8df1c6438575a52c127e4881570868185d5be1b88ff7ce4a8756b17a2c3</cites><orcidid>0000-0003-1531-8567</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1043466624001868$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38943738$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ahmed Salıh Gezh, Shahab</creatorcontrib><creatorcontrib>Deveci, Koksal</creatorcontrib><creatorcontrib>Sivgin, Hakan</creatorcontrib><creatorcontrib>Guzelgul, Figen</creatorcontrib><title>Serum L C3-II levels in type 2 diabetic patients with impaired renal functions</title><title>Cytokine (Philadelphia, Pa.)</title><addtitle>Cytokine</addtitle><description>A total of 176 Turkish subjects were enrolled, of whom 26 were healthy, and 150 had type 2 diabetes mellitus. Under the light of American Diabetes Association criteria, we selected 150 patients and introduced them as type 2 DM. Patients were classified according to albumin urea ratio: 88 patients had macroalbuminuria (ACR > 300 mg/g), 20 patients had microalbuminuria (ACR between 30 and 300 mg/g), and 42 had normoalbuminuria (ACR < 30 mg/g). According to eGFR values, T2DM patients were divided into six categories [standard to high (G1), slightly decreased (G2), slightly to moderately decreased (G3a), moderate to severely decreased (G3b), severely decreased (G4), and renal failure (G5)]. Proteinuria severity and eGFR stages were evaluated together and divided into three groups (Stage 1: Normoalbuminuria+G1/G2, Stage 2: Microalbuminuria+G3a/G3b, Stage 3: Macroalbuminuria+G5/G4).
There is no relationship between LC3-II levels and ACR in T2DM patients.
LC3-II has sufficient performance in the differential diagnosis of severe proteinuria.
[Display omitted]
•LC3-II levels were high in type 2 DM patients with DKD.•LC3-II elevation is higher in patients with severe proteinuria and advanced stage DKD.•The increase in LC3-II is accompanied by an increase in BCL-2 and TGF-β1.•The reason for the decrease in IL-1β in DKD may be inhibition due to the increase in LC3-II.•The increase in LC3-II can prevent tubular apoptosis by inhibiting the decrease in BCL-2.•Podocin levels are related to LC3-II in DKD patients.
This study was designed to evaluate serum LC3-II, BCL-2, IL-1β, TGF-β1, and podocin levels in.
type 2 diabetes (T2DM) patients with renal dysfunction.
176 Turkish subjects were enrolled, of whom 26 were healthy, and 150 had T2DM. Patients.
were classified according to albumin urea ratio: 88 patients had macroalbuminuria, 20.
patients had microalbuminuria, and 42 had normoalbuminuria. T2DM patients were also.
classified into three groups according to proteinuria and eGFR stages.
Increased serum LC3-II levels in patients with T2DM with increased urinary albumin.
extraction and impaired renal functions. There was a strong relationship between serum.
LC3-II levels and serum BCL-2, IL-1β, TGF-β1, and Podocin levels. The efficiency of LC3-
II as a diagnostic biomarker in the differential diagnosis of DM patients with.
macroproteinuria from DM patients with normoproteinuria was 75.4%.
It was thought that increased serum LC3-II levels in T2DM patients with impaired renal.
functions may cause renal podocyte damage. In these patients, serum LC3-II levels can be.
evaluated as a new biomarker to follow the development of renal damage.</description><subject>Adult</subject><subject>Aged</subject><subject>Albuminuria - blood</subject><subject>Autophagy</subject><subject>BCL-2</subject><subject>Biomarkers - blood</subject><subject>Diabetes Mellitus, Type 2 - blood</subject><subject>Diabetes Mellitus, Type 2 - complications</subject><subject>Diabetic Nephropathies - blood</subject><subject>Diabetic Nephropathies - physiopathology</subject><subject>DKD</subject><subject>Female</subject><subject>Glomerular Filtration Rate</subject><subject>Humans</subject><subject>Interleukin-1beta - blood</subject><subject>Intracellular Signaling Peptides and Proteins</subject><subject>Kidney - physiopathology</subject><subject>LC3-II</subject><subject>Male</subject><subject>Membrane Proteins - blood</subject><subject>Microtubule-Associated Proteins</subject><subject>Middle Aged</subject><subject>Podocin</subject><subject>Proteinuria</subject><subject>Proto-Oncogene Proteins c-bcl-2 - blood</subject><subject>Transforming Growth Factor beta1 - blood</subject><issn>1043-4666</issn><issn>1096-0023</issn><issn>1096-0023</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp90MtKAzEUBuAgiq3VF3AhWbqZmtskKbiR4qVQdKGuQyZzBlPmZpJR-vZOaXXp6pzFf_4DH0KXlMwpofJmM3fb1M0ZYWJOcyk1P0JTShYyI4Tx490ueCaklBN0FuOGELLgSp2iCdcLwRXXU_T8CmFo8BovebZa4Rq-oI7Ytzhte8AMl94WkLzDvU0e2hTxt08f2De99QFKHKC1Na6G1iXftfEcnVS2jnBxmDP0_nD_tnzK1i-Pq-XdOnOcqJQJYIV2uqyok4LrXOU2Z44yBUJrmiuipaY6L_MCaKF1VSkHwmqVy4Iqyxyfoet9bx-6zwFiMo2PDurattAN0YxfuKJ8IcgYZfuoC12MASrTB9_YsDWUmJ2j2Zido9k5mr3jeHR16B-KBsq_k1-4MXC7D4xc8OUhmOhGHwflyOKSKTv_X_8PRVuCUA</recordid><startdate>202409</startdate><enddate>202409</enddate><creator>Ahmed Salıh Gezh, Shahab</creator><creator>Deveci, Koksal</creator><creator>Sivgin, Hakan</creator><creator>Guzelgul, Figen</creator><general>Elsevier Ltd</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>7X8</scope><orcidid>https://orcid.org/0000-0003-1531-8567</orcidid></search><sort><creationdate>202409</creationdate><title>Serum L C3-II levels in type 2 diabetic patients with impaired renal functions</title><author>Ahmed Salıh Gezh, Shahab ; Deveci, Koksal ; Sivgin, Hakan ; Guzelgul, Figen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c307t-4e2b8c8df1c6438575a52c127e4881570868185d5be1b88ff7ce4a8756b17a2c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Albuminuria - blood</topic><topic>Autophagy</topic><topic>BCL-2</topic><topic>Biomarkers - blood</topic><topic>Diabetes Mellitus, Type 2 - blood</topic><topic>Diabetes Mellitus, Type 2 - complications</topic><topic>Diabetic Nephropathies - blood</topic><topic>Diabetic Nephropathies - physiopathology</topic><topic>DKD</topic><topic>Female</topic><topic>Glomerular Filtration Rate</topic><topic>Humans</topic><topic>Interleukin-1beta - blood</topic><topic>Intracellular Signaling Peptides and Proteins</topic><topic>Kidney - physiopathology</topic><topic>LC3-II</topic><topic>Male</topic><topic>Membrane Proteins - blood</topic><topic>Microtubule-Associated Proteins</topic><topic>Middle Aged</topic><topic>Podocin</topic><topic>Proteinuria</topic><topic>Proto-Oncogene Proteins c-bcl-2 - blood</topic><topic>Transforming Growth Factor beta1 - blood</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ahmed Salıh Gezh, Shahab</creatorcontrib><creatorcontrib>Deveci, Koksal</creatorcontrib><creatorcontrib>Sivgin, Hakan</creatorcontrib><creatorcontrib>Guzelgul, Figen</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Cytokine (Philadelphia, Pa.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ahmed Salıh Gezh, Shahab</au><au>Deveci, Koksal</au><au>Sivgin, Hakan</au><au>Guzelgul, Figen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Serum L C3-II levels in type 2 diabetic patients with impaired renal functions</atitle><jtitle>Cytokine (Philadelphia, Pa.)</jtitle><addtitle>Cytokine</addtitle><date>2024-09</date><risdate>2024</risdate><volume>181</volume><spage>156683</spage><pages>156683-</pages><artnum>156683</artnum><issn>1043-4666</issn><issn>1096-0023</issn><eissn>1096-0023</eissn><abstract>A total of 176 Turkish subjects were enrolled, of whom 26 were healthy, and 150 had type 2 diabetes mellitus. Under the light of American Diabetes Association criteria, we selected 150 patients and introduced them as type 2 DM. Patients were classified according to albumin urea ratio: 88 patients had macroalbuminuria (ACR > 300 mg/g), 20 patients had microalbuminuria (ACR between 30 and 300 mg/g), and 42 had normoalbuminuria (ACR < 30 mg/g). According to eGFR values, T2DM patients were divided into six categories [standard to high (G1), slightly decreased (G2), slightly to moderately decreased (G3a), moderate to severely decreased (G3b), severely decreased (G4), and renal failure (G5)]. Proteinuria severity and eGFR stages were evaluated together and divided into three groups (Stage 1: Normoalbuminuria+G1/G2, Stage 2: Microalbuminuria+G3a/G3b, Stage 3: Macroalbuminuria+G5/G4).
There is no relationship between LC3-II levels and ACR in T2DM patients.
LC3-II has sufficient performance in the differential diagnosis of severe proteinuria.
[Display omitted]
•LC3-II levels were high in type 2 DM patients with DKD.•LC3-II elevation is higher in patients with severe proteinuria and advanced stage DKD.•The increase in LC3-II is accompanied by an increase in BCL-2 and TGF-β1.•The reason for the decrease in IL-1β in DKD may be inhibition due to the increase in LC3-II.•The increase in LC3-II can prevent tubular apoptosis by inhibiting the decrease in BCL-2.•Podocin levels are related to LC3-II in DKD patients.
This study was designed to evaluate serum LC3-II, BCL-2, IL-1β, TGF-β1, and podocin levels in.
type 2 diabetes (T2DM) patients with renal dysfunction.
176 Turkish subjects were enrolled, of whom 26 were healthy, and 150 had T2DM. Patients.
were classified according to albumin urea ratio: 88 patients had macroalbuminuria, 20.
patients had microalbuminuria, and 42 had normoalbuminuria. T2DM patients were also.
classified into three groups according to proteinuria and eGFR stages.
Increased serum LC3-II levels in patients with T2DM with increased urinary albumin.
extraction and impaired renal functions. There was a strong relationship between serum.
LC3-II levels and serum BCL-2, IL-1β, TGF-β1, and Podocin levels. The efficiency of LC3-
II as a diagnostic biomarker in the differential diagnosis of DM patients with.
macroproteinuria from DM patients with normoproteinuria was 75.4%.
It was thought that increased serum LC3-II levels in T2DM patients with impaired renal.
functions may cause renal podocyte damage. In these patients, serum LC3-II levels can be.
evaluated as a new biomarker to follow the development of renal damage.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>38943738</pmid><doi>10.1016/j.cyto.2024.156683</doi><orcidid>https://orcid.org/0000-0003-1531-8567</orcidid></addata></record> |
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source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | Adult Aged Albuminuria - blood Autophagy BCL-2 Biomarkers - blood Diabetes Mellitus, Type 2 - blood Diabetes Mellitus, Type 2 - complications Diabetic Nephropathies - blood Diabetic Nephropathies - physiopathology DKD Female Glomerular Filtration Rate Humans Interleukin-1beta - blood Intracellular Signaling Peptides and Proteins Kidney - physiopathology LC3-II Male Membrane Proteins - blood Microtubule-Associated Proteins Middle Aged Podocin Proteinuria Proto-Oncogene Proteins c-bcl-2 - blood Transforming Growth Factor beta1 - blood |
title | Serum L C3-II levels in type 2 diabetic patients with impaired renal functions |
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