<?xml version="1.0" encoding="UTF-8" ?>
<oai_dc:dc schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
<dc:title>A common APOE polymorphism is an independent risk factor for reduced glomerular filtration rate in the Spanish RENASTUR cohort</dc:title>
<dc:creator>Gómez, Juan</dc:creator>
<dc:creator>Tavira, Beatriz</dc:creator>
<dc:creator>Tranche, Salvador</dc:creator>
<dc:creator>Ortega, Francisco</dc:creator>
<dc:creator>Rodríguez, M. Isabel</dc:creator>
<dc:creator>Sánchez, Emilio</dc:creator>
<dc:creator>Marín, Rafael</dc:creator>
<dc:creator>Corao, Ana I.</dc:creator>
<dc:creator>Arenas, Jorge</dc:creator>
<dc:creator>Álvarez, Victoria</dc:creator>
<dc:subject>APOE polymorphisms</dc:subject>
<dc:subject>Type 2 diabetes mellitus glomerular filtration</dc:subject>
<dc:subject>Renal function</dc:subject>
<dc:description>Objective. APOE gene variants may contribute to risk of chronic kidney disease. Our aim was to determine whether the common APOE-ε2/ε3/ε4 polymorphism was associated with reduced estimated glomerular filtration rate (eGFR) in the Renastur population, a cohort of elderly individuals from the region Asturias (Northern Spain). Methods. A total of 743 Spanish Caucasian aged 55-85 were genotyped for the APOE-ε2/ ε3/ ε4 polymorphisms. Individuals with a previous diagnostic of renal disease were not eligible for the study. Participants with a documented history of type 2 diabetes (T2DM) or hypertension or who were receiving antidiabetic or antihypertensive drugs were classified as diabetics and hypertensives. The eGFR was calculated with the Modification of Diet in Renal Disease formulae, and those with an eGFR <60 ml/min/1.73 m2 (n=91) were considered as having renal impaired function. The effect of alleles and genotypes on clinical (hypertension, diabetes) and analytical findings was statistically determined. Results. In addition to age and T2DM, APOE-ε2 was significantly associated with eGFR<60 (p=0.002; OR= 2.30). This association remained statistically significant after correction by multiple variants. Although the effect of the APOE-ε2 on eGFR was seen among diabetics and non diabetics, the significance was stronger in the T2DM group Conclusion. The APOE-ε2 allele was a genetic risk factor for impaired renal function among healthy Spanish elderly individuals.</dc:description>
<dc:description>This work was supported by Red de Investigación Renal-REDINREN and Fondo de Investigaciones Sanitarias (grant 10/01971 to FO).</dc:description>
<dc:date>2013-04-16T08:31:35Z</dc:date>
<dc:date>2013-04-16T08:31:35Z</dc:date>
<dc:date>2013</dc:date>
<dc:type>postprint</dc:type>
<dc:identifier>https://ria.asturias.es/RIA/handle/123456789/2741</dc:identifier>
<dc:language>eng</dc:language>
<dc:relation>No, esta versión no ha sido citada</dc:relation>
<dc:rights>http://creativecommons.org/licenses/by-nc-sa/3.0/deed.es</dc:rights>
<dc:format>application/pdf</dc:format>
</oai_dc:dc>
<?xml version="1.0" encoding="UTF-8" ?>
<d:DIDL schemaLocation="urn:mpeg:mpeg21:2002:02-DIDL-NS http://standards.iso.org/ittf/PubliclyAvailableStandards/MPEG-21_schema_files/did/didl.xsd">
<d:DIDLInfo>
<dcterms:created schemaLocation="http://purl.org/dc/terms/ http://dublincore.org/schemas/xmls/qdc/dcterms.xsd">2013-04-16T08:31:35Z</dcterms:created>
</d:DIDLInfo>
<d:Item id="hdl_123456789_2741">
<d:Descriptor>
<d:Statement mimeType="application/xml; charset=utf-8">
<dii:Identifier schemaLocation="urn:mpeg:mpeg21:2002:01-DII-NS http://standards.iso.org/ittf/PubliclyAvailableStandards/MPEG-21_schema_files/dii/dii.xsd">urn:hdl:123456789/2741</dii:Identifier>
</d:Statement>
</d:Descriptor>
<d:Descriptor>
<d:Statement mimeType="application/xml; charset=utf-8">
<oai_dc:dc schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
<dc:title>A common APOE polymorphism is an independent risk factor for reduced glomerular filtration rate in the Spanish RENASTUR cohort</dc:title>
<dc:creator>Gómez, Juan</dc:creator>
<dc:creator>Tavira, Beatriz</dc:creator>
<dc:creator>Tranche, Salvador</dc:creator>
<dc:creator>Ortega, Francisco</dc:creator>
<dc:creator>Rodríguez, M. Isabel</dc:creator>
<dc:creator>Sánchez, Emilio</dc:creator>
<dc:creator>Marín, Rafael</dc:creator>
<dc:creator>Corao, Ana I.</dc:creator>
<dc:creator>Arenas, Jorge</dc:creator>
<dc:creator>Álvarez, Victoria</dc:creator>
<dc:subject>APOE polymorphisms</dc:subject>
<dc:subject>Type 2 diabetes mellitus glomerular filtration</dc:subject>
<dc:subject>Renal function</dc:subject>
<dc:description>Objective. APOE gene variants may contribute to risk of chronic kidney disease. Our aim was to determine whether the common APOE-ε2/ε3/ε4 polymorphism was associated with reduced estimated glomerular filtration rate (eGFR) in the Renastur population, a cohort of elderly individuals from the region Asturias (Northern Spain). Methods. A total of 743 Spanish Caucasian aged 55-85 were genotyped for the APOE-ε2/ ε3/ ε4 polymorphisms. Individuals with a previous diagnostic of renal disease were not eligible for the study. Participants with a documented history of type 2 diabetes (T2DM) or hypertension or who were receiving antidiabetic or antihypertensive drugs were classified as diabetics and hypertensives. The eGFR was calculated with the Modification of Diet in Renal Disease formulae, and those with an eGFR <60 ml/min/1.73 m2 (n=91) were considered as having renal impaired function. The effect of alleles and genotypes on clinical (hypertension, diabetes) and analytical findings was statistically determined. Results. In addition to age and T2DM, APOE-ε2 was significantly associated with eGFR<60 (p=0.002; OR= 2.30). This association remained statistically significant after correction by multiple variants. Although the effect of the APOE-ε2 on eGFR was seen among diabetics and non diabetics, the significance was stronger in the T2DM group Conclusion. The APOE-ε2 allele was a genetic risk factor for impaired renal function among healthy Spanish elderly individuals.</dc:description>
<dc:date>2013-04-16T08:31:35Z</dc:date>
<dc:date>2013-04-16T08:31:35Z</dc:date>
<dc:date>2013</dc:date>
<dc:type>postprint</dc:type>
<dc:identifier>https://ria.asturias.es/RIA/handle/123456789/2741</dc:identifier>
<dc:language>eng</dc:language>
<dc:relation>No, esta versión no ha sido citada</dc:relation>
<dc:rights>http://creativecommons.org/licenses/by-nc-sa/3.0/deed.es</dc:rights>
</oai_dc:dc>
</d:Statement>
</d:Descriptor>
<d:Component id="123456789_2741_1">
</d:Component>
</d:Item>
</d:DIDL>
<?xml version="1.0" encoding="UTF-8" ?>
<dim:dim schemaLocation="http://www.dspace.org/xmlns/dspace/dim http://www.dspace.org/schema/dim.xsd">
<dim:field element="contributor" mdschema="dc" qualifier="author">Gómez, Juan</dim:field>
<dim:field element="contributor" mdschema="dc" qualifier="author">Tavira, Beatriz</dim:field>
<dim:field element="contributor" mdschema="dc" qualifier="author">Tranche, Salvador</dim:field>
<dim:field element="contributor" mdschema="dc" qualifier="author">Ortega, Francisco</dim:field>
<dim:field element="contributor" mdschema="dc" qualifier="author">Rodríguez, M. Isabel</dim:field>
<dim:field element="contributor" mdschema="dc" qualifier="author">Sánchez, Emilio</dim:field>
<dim:field element="contributor" mdschema="dc" qualifier="author">Marín, Rafael</dim:field>
<dim:field element="contributor" mdschema="dc" qualifier="author">Corao, Ana I.</dim:field>
<dim:field element="contributor" mdschema="dc" qualifier="author">Arenas, Jorge</dim:field>
<dim:field element="contributor" mdschema="dc" qualifier="author">Álvarez, Victoria</dim:field>
<dim:field element="date" mdschema="dc" qualifier="accessioned">2013-04-16T08:31:35Z</dim:field>
<dim:field element="date" mdschema="dc" qualifier="available">2013-04-16T08:31:35Z</dim:field>
<dim:field element="date" mdschema="dc" qualifier="issued">2013</dim:field>
<dim:field element="identifier" mdschema="dc" qualifier="uri">https://ria.asturias.es/RIA/handle/123456789/2741</dim:field>
<dim:field element="description" lang="eng" mdschema="dc" qualifier="abstract">Objective. APOE gene variants may contribute to risk of chronic kidney disease. Our aim was to determine whether the common APOE-ε2/ε3/ε4 polymorphism was associated with reduced estimated glomerular filtration rate (eGFR) in the Renastur population, a cohort of elderly individuals from the region Asturias (Northern Spain). Methods. A total of 743 Spanish Caucasian aged 55-85 were genotyped for the APOE-ε2/ ε3/ ε4 polymorphisms. Individuals with a previous diagnostic of renal disease were not eligible for the study. Participants with a documented history of type 2 diabetes (T2DM) or hypertension or who were receiving antidiabetic or antihypertensive drugs were classified as diabetics and hypertensives. The eGFR was calculated with the Modification of Diet in Renal Disease formulae, and those with an eGFR <60 ml/min/1.73 m2 (n=91) were considered as having renal impaired function. The effect of alleles and genotypes on clinical (hypertension, diabetes) and analytical findings was statistically determined. Results. In addition to age and T2DM, APOE-ε2 was significantly associated with eGFR<60 (p=0.002; OR= 2.30). This association remained statistically significant after correction by multiple variants. Although the effect of the APOE-ε2 on eGFR was seen among diabetics and non diabetics, the significance was stronger in the T2DM group Conclusion. The APOE-ε2 allele was a genetic risk factor for impaired renal function among healthy Spanish elderly individuals.</dim:field>
<dim:field element="description" lang="eng" mdschema="dc" qualifier="sponsorship">This work was supported by Red de Investigación Renal-REDINREN and Fondo de Investigaciones Sanitarias (grant 10/01971 to FO).</dim:field>
<dim:field element="language" lang="eng" mdschema="dc" qualifier="iso">eng</dim:field>
<dim:field element="relation" lang="eng" mdschema="dc" qualifier="isreferencedby">No, esta versión no ha sido citada</dim:field>
<dim:field element="rights" lang="eng" mdschema="dc">http://creativecommons.org/licenses/by-nc-sa/3.0/deed.es</dim:field>
<dim:field element="subject" lang="eng" mdschema="dc">APOE polymorphisms</dim:field>
<dim:field element="subject" lang="eng" mdschema="dc">Type 2 diabetes mellitus glomerular filtration</dim:field>
<dim:field element="subject" lang="eng" mdschema="dc">Renal function</dim:field>
<dim:field element="title" lang="eng" mdschema="dc">A common APOE polymorphism is an independent risk factor for reduced glomerular filtration rate in the Spanish RENASTUR cohort</dim:field>
<dim:field element="type" lang="eng" mdschema="dc">postprint</dim:field>
</dim:dim>
<?xml version="1.0" encoding="UTF-8" ?>
<thesis schemaLocation="http://www.ndltd.org/standards/metadata/etdms/1.0/ http://www.ndltd.org/standards/metadata/etdms/1.0/etdms.xsd">
<title>A common APOE polymorphism is an independent risk factor for reduced glomerular filtration rate in the Spanish RENASTUR cohort</title>
<creator>Gómez, Juan</creator>
<creator>Tavira, Beatriz</creator>
<creator>Tranche, Salvador</creator>
<creator>Ortega, Francisco</creator>
<creator>Rodríguez, M. Isabel</creator>
<creator>Sánchez, Emilio</creator>
<creator>Marín, Rafael</creator>
<creator>Corao, Ana I.</creator>
<creator>Arenas, Jorge</creator>
<creator>Álvarez, Victoria</creator>
<subject>APOE polymorphisms</subject>
<subject>Type 2 diabetes mellitus glomerular filtration</subject>
<subject>Renal function</subject>
<description>Objective. APOE gene variants may contribute to risk of chronic kidney disease. Our aim was to determine whether the common APOE-ε2/ε3/ε4 polymorphism was associated with reduced estimated glomerular filtration rate (eGFR) in the Renastur population, a cohort of elderly individuals from the region Asturias (Northern Spain). Methods. A total of 743 Spanish Caucasian aged 55-85 were genotyped for the APOE-ε2/ ε3/ ε4 polymorphisms. Individuals with a previous diagnostic of renal disease were not eligible for the study. Participants with a documented history of type 2 diabetes (T2DM) or hypertension or who were receiving antidiabetic or antihypertensive drugs were classified as diabetics and hypertensives. The eGFR was calculated with the Modification of Diet in Renal Disease formulae, and those with an eGFR <60 ml/min/1.73 m2 (n=91) were considered as having renal impaired function. The effect of alleles and genotypes on clinical (hypertension, diabetes) and analytical findings was statistically determined. Results. In addition to age and T2DM, APOE-ε2 was significantly associated with eGFR<60 (p=0.002; OR= 2.30). This association remained statistically significant after correction by multiple variants. Although the effect of the APOE-ε2 on eGFR was seen among diabetics and non diabetics, the significance was stronger in the T2DM group Conclusion. The APOE-ε2 allele was a genetic risk factor for impaired renal function among healthy Spanish elderly individuals.</description>
<date>2013-04-16</date>
<date>2013-04-16</date>
<date>2013</date>
<type>postprint</type>
<identifier>https://ria.asturias.es/RIA/handle/123456789/2741</identifier>
<language>eng</language>
<relation>No, esta versión no ha sido citada</relation>
<rights>http://creativecommons.org/licenses/by-nc-sa/3.0/deed.es</rights>
</thesis>
<?xml version="1.0" encoding="UTF-8" ?>
<record schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
<leader>00925njm 22002777a 4500</leader>
<datafield ind1=" " ind2=" " tag="042">
<subfield code="a">dc</subfield>
</datafield>
<datafield ind1=" " ind2=" " tag="720">
<subfield code="a">Gómez, Juan</subfield>
<subfield code="e">author</subfield>
</datafield>
<datafield ind1=" " ind2=" " tag="720">
<subfield code="a">Tavira, Beatriz</subfield>
<subfield code="e">author</subfield>
</datafield>
<datafield ind1=" " ind2=" " tag="720">
<subfield code="a">Tranche, Salvador</subfield>
<subfield code="e">author</subfield>
</datafield>
<datafield ind1=" " ind2=" " tag="720">
<subfield code="a">Ortega, Francisco</subfield>
<subfield code="e">author</subfield>
</datafield>
<datafield ind1=" " ind2=" " tag="720">
<subfield code="a">Rodríguez, M. Isabel</subfield>
<subfield code="e">author</subfield>
</datafield>
<datafield ind1=" " ind2=" " tag="720">
<subfield code="a">Sánchez, Emilio</subfield>
<subfield code="e">author</subfield>
</datafield>
<datafield ind1=" " ind2=" " tag="720">
<subfield code="a">Marín, Rafael</subfield>
<subfield code="e">author</subfield>
</datafield>
<datafield ind1=" " ind2=" " tag="720">
<subfield code="a">Corao, Ana I.</subfield>
<subfield code="e">author</subfield>
</datafield>
<datafield ind1=" " ind2=" " tag="720">
<subfield code="a">Arenas, Jorge</subfield>
<subfield code="e">author</subfield>
</datafield>
<datafield ind1=" " ind2=" " tag="720">
<subfield code="a">Álvarez, Victoria</subfield>
<subfield code="e">author</subfield>
</datafield>
<datafield ind1=" " ind2=" " tag="260">
<subfield code="c">2013</subfield>
</datafield>
<datafield ind1=" " ind2=" " tag="520">
<subfield code="a">Objective. APOE gene variants may contribute to risk of chronic kidney disease. Our aim was to determine whether the common APOE-ε2/ε3/ε4 polymorphism was associated with reduced estimated glomerular filtration rate (eGFR) in the Renastur population, a cohort of elderly individuals from the region Asturias (Northern Spain). Methods. A total of 743 Spanish Caucasian aged 55-85 were genotyped for the APOE-ε2/ ε3/ ε4 polymorphisms. Individuals with a previous diagnostic of renal disease were not eligible for the study. Participants with a documented history of type 2 diabetes (T2DM) or hypertension or who were receiving antidiabetic or antihypertensive drugs were classified as diabetics and hypertensives. The eGFR was calculated with the Modification of Diet in Renal Disease formulae, and those with an eGFR <60 ml/min/1.73 m2 (n=91) were considered as having renal impaired function. The effect of alleles and genotypes on clinical (hypertension, diabetes) and analytical findings was statistically determined. Results. In addition to age and T2DM, APOE-ε2 was significantly associated with eGFR<60 (p=0.002; OR= 2.30). This association remained statistically significant after correction by multiple variants. Although the effect of the APOE-ε2 on eGFR was seen among diabetics and non diabetics, the significance was stronger in the T2DM group Conclusion. The APOE-ε2 allele was a genetic risk factor for impaired renal function among healthy Spanish elderly individuals.</subfield>
</datafield>
<datafield ind1="8" ind2=" " tag="024">
<subfield code="a">https://ria.asturias.es/RIA/handle/123456789/2741</subfield>
</datafield>
<datafield ind1=" " ind2=" " tag="653">
<subfield code="a">APOE polymorphisms</subfield>
</datafield>
<datafield ind1=" " ind2=" " tag="653">
<subfield code="a">Type 2 diabetes mellitus glomerular filtration</subfield>
</datafield>
<datafield ind1=" " ind2=" " tag="653">
<subfield code="a">Renal function</subfield>
</datafield>
<datafield ind1="0" ind2="0" tag="245">
<subfield code="a">A common APOE polymorphism is an independent risk factor for reduced glomerular filtration rate in the Spanish RENASTUR cohort</subfield>
</datafield>
</record>
<?xml version="1.0" encoding="UTF-8" ?>
<mets ID=" DSpace_ITEM_123456789-2741" OBJID=" hdl:123456789/2741" PROFILE="DSpace METS SIP Profile 1.0" TYPE="DSpace ITEM" schemaLocation="http://www.loc.gov/METS/ http://www.loc.gov/standards/mets/mets.xsd">
<metsHdr CREATEDATE="2023-01-14T18:25:44Z">
<agent ROLE="CUSTODIAN" TYPE="ORGANIZATION">
<name>RIA</name>
</agent>
</metsHdr>
<dmdSec ID="DMD_123456789_2741">
<mdWrap MDTYPE="MODS">
<xmlData schemaLocation="http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-1.xsd">
<mods:mods schemaLocation="http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-1.xsd">
<mods:name>
<mods:role>
<mods:roleTerm type="text">author</mods:roleTerm>
</mods:role>
<mods:namePart>Gómez, Juan</mods:namePart>
</mods:name>
<mods:name>
<mods:role>
<mods:roleTerm type="text">author</mods:roleTerm>
</mods:role>
<mods:namePart>Tavira, Beatriz</mods:namePart>
</mods:name>
<mods:name>
<mods:role>
<mods:roleTerm type="text">author</mods:roleTerm>
</mods:role>
<mods:namePart>Tranche, Salvador</mods:namePart>
</mods:name>
<mods:name>
<mods:role>
<mods:roleTerm type="text">author</mods:roleTerm>
</mods:role>
<mods:namePart>Ortega, Francisco</mods:namePart>
</mods:name>
<mods:name>
<mods:role>
<mods:roleTerm type="text">author</mods:roleTerm>
</mods:role>
<mods:namePart>Rodríguez, M. Isabel</mods:namePart>
</mods:name>
<mods:name>
<mods:role>
<mods:roleTerm type="text">author</mods:roleTerm>
</mods:role>
<mods:namePart>Sánchez, Emilio</mods:namePart>
</mods:name>
<mods:name>
<mods:role>
<mods:roleTerm type="text">author</mods:roleTerm>
</mods:role>
<mods:namePart>Marín, Rafael</mods:namePart>
</mods:name>
<mods:name>
<mods:role>
<mods:roleTerm type="text">author</mods:roleTerm>
</mods:role>
<mods:namePart>Corao, Ana I.</mods:namePart>
</mods:name>
<mods:name>
<mods:role>
<mods:roleTerm type="text">author</mods:roleTerm>
</mods:role>
<mods:namePart>Arenas, Jorge</mods:namePart>
</mods:name>
<mods:name>
<mods:role>
<mods:roleTerm type="text">author</mods:roleTerm>
</mods:role>
<mods:namePart>Álvarez, Victoria</mods:namePart>
</mods:name>
<mods:extension>
<mods:dateAccessioned encoding="iso8601">2013-04-16T08:31:35Z</mods:dateAccessioned>
</mods:extension>
<mods:extension>
<mods:dateAvailable encoding="iso8601">2013-04-16T08:31:35Z</mods:dateAvailable>
</mods:extension>
<mods:originInfo>
<mods:dateIssued encoding="iso8601">2013</mods:dateIssued>
</mods:originInfo>
<mods:identifier type="uri">https://ria.asturias.es/RIA/handle/123456789/2741</mods:identifier>
<mods:abstract>Objective. APOE gene variants may contribute to risk of chronic kidney disease. Our aim was to determine whether the common APOE-ε2/ε3/ε4 polymorphism was associated with reduced estimated glomerular filtration rate (eGFR) in the Renastur population, a cohort of elderly individuals from the region Asturias (Northern Spain). Methods. A total of 743 Spanish Caucasian aged 55-85 were genotyped for the APOE-ε2/ ε3/ ε4 polymorphisms. Individuals with a previous diagnostic of renal disease were not eligible for the study. Participants with a documented history of type 2 diabetes (T2DM) or hypertension or who were receiving antidiabetic or antihypertensive drugs were classified as diabetics and hypertensives. The eGFR was calculated with the Modification of Diet in Renal Disease formulae, and those with an eGFR <60 ml/min/1.73 m2 (n=91) were considered as having renal impaired function. The effect of alleles and genotypes on clinical (hypertension, diabetes) and analytical findings was statistically determined. Results. In addition to age and T2DM, APOE-ε2 was significantly associated with eGFR<60 (p=0.002; OR= 2.30). This association remained statistically significant after correction by multiple variants. Although the effect of the APOE-ε2 on eGFR was seen among diabetics and non diabetics, the significance was stronger in the T2DM group Conclusion. The APOE-ε2 allele was a genetic risk factor for impaired renal function among healthy Spanish elderly individuals.</mods:abstract>
<mods:language>
<mods:languageTerm authority="rfc3066">eng</mods:languageTerm>
</mods:language>
<mods:accessCondition type="useAndReproduction">http://creativecommons.org/licenses/by-nc-sa/3.0/deed.es</mods:accessCondition>
<mods:subject>
<mods:topic>APOE polymorphisms</mods:topic>
</mods:subject>
<mods:subject>
<mods:topic>Type 2 diabetes mellitus glomerular filtration</mods:topic>
</mods:subject>
<mods:subject>
<mods:topic>Renal function</mods:topic>
</mods:subject>
<mods:titleInfo>
<mods:title>A common APOE polymorphism is an independent risk factor for reduced glomerular filtration rate in the Spanish RENASTUR cohort</mods:title>
</mods:titleInfo>
<mods:genre>postprint</mods:genre>
</mods:mods>
</xmlData>
</mdWrap>
</dmdSec>
<amdSec ID="FO_123456789_2741_1">
<techMD ID="TECH_O_123456789_2741_1">
<mdWrap MDTYPE="PREMIS">
<xmlData schemaLocation="http://www.loc.gov/standards/premis http://www.loc.gov/standards/premis/PREMIS-v1-0.xsd">
<premis:premis>
<premis:object>
<premis:objectIdentifier>
<premis:objectIdentifierType>URL</premis:objectIdentifierType>
<premis:objectIdentifierValue>http://172.28.36.237:8080/jspui/bitstream/123456789/2741/1/Archivo.pdf</premis:objectIdentifierValue>
</premis:objectIdentifier>
<premis:objectCategory>File</premis:objectCategory>
<premis:objectCharacteristics>
<premis:fixity>
<premis:messageDigestAlgorithm>MD5</premis:messageDigestAlgorithm>
<premis:messageDigest>dc3e800945716acf991a50bd1d82d8ca</premis:messageDigest>
</premis:fixity>
<premis:size>217928</premis:size>
<premis:format>
<premis:formatDesignation>
<premis:formatName>application/pdf</premis:formatName>
</premis:formatDesignation>
</premis:format>
</premis:objectCharacteristics>
<premis:originalName>Archivo.pdf</premis:originalName>
</premis:object>
</premis:premis>
</xmlData>
</mdWrap>
</techMD>
</amdSec>
<fileSec>
<fileGrp USE="ORIGINAL">
<file ADMID="FO_123456789_2741_1" CHECKSUM="dc3e800945716acf991a50bd1d82d8ca" CHECKSUMTYPE="MD5" GROUPID="GROUP_BITSTREAM_123456789_2741_1" ID="BITSTREAM_ORIGINAL_123456789_2741_1" MIMETYPE="application/pdf" SEQ="1" SIZE="217928">
</file>
</fileGrp>
</fileSec>
<structMap LABEL="DSpace Object" TYPE="LOGICAL">
<div ADMID="DMD_123456789_2741" TYPE="DSpace Object Contents">
<div TYPE="DSpace BITSTREAM">
</div>
</div>
</structMap>
</mets>
<?xml version="1.0" encoding="UTF-8" ?>
<mods:mods schemaLocation="http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-1.xsd">
<mods:name>
<mods:namePart>Gómez, Juan</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>Tavira, Beatriz</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>Tranche, Salvador</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>Ortega, Francisco</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>Rodríguez, M. Isabel</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>Sánchez, Emilio</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>Marín, Rafael</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>Corao, Ana I.</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>Arenas, Jorge</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>Álvarez, Victoria</mods:namePart>
</mods:name>
<mods:extension>
<mods:dateAvailable encoding="iso8601">2013-04-16T08:31:35Z</mods:dateAvailable>
</mods:extension>
<mods:extension>
<mods:dateAccessioned encoding="iso8601">2013-04-16T08:31:35Z</mods:dateAccessioned>
</mods:extension>
<mods:originInfo>
<mods:dateIssued encoding="iso8601">2013</mods:dateIssued>
</mods:originInfo>
<mods:identifier type="uri">https://ria.asturias.es/RIA/handle/123456789/2741</mods:identifier>
<mods:abstract>Objective. APOE gene variants may contribute to risk of chronic kidney disease. Our aim was to determine whether the common APOE-ε2/ε3/ε4 polymorphism was associated with reduced estimated glomerular filtration rate (eGFR) in the Renastur population, a cohort of elderly individuals from the region Asturias (Northern Spain). Methods. A total of 743 Spanish Caucasian aged 55-85 were genotyped for the APOE-ε2/ ε3/ ε4 polymorphisms. Individuals with a previous diagnostic of renal disease were not eligible for the study. Participants with a documented history of type 2 diabetes (T2DM) or hypertension or who were receiving antidiabetic or antihypertensive drugs were classified as diabetics and hypertensives. The eGFR was calculated with the Modification of Diet in Renal Disease formulae, and those with an eGFR <60 ml/min/1.73 m2 (n=91) were considered as having renal impaired function. The effect of alleles and genotypes on clinical (hypertension, diabetes) and analytical findings was statistically determined. Results. In addition to age and T2DM, APOE-ε2 was significantly associated with eGFR<60 (p=0.002; OR= 2.30). This association remained statistically significant after correction by multiple variants. Although the effect of the APOE-ε2 on eGFR was seen among diabetics and non diabetics, the significance was stronger in the T2DM group Conclusion. The APOE-ε2 allele was a genetic risk factor for impaired renal function among healthy Spanish elderly individuals.</mods:abstract>
<mods:language>
<mods:languageTerm>eng</mods:languageTerm>
</mods:language>
<mods:accessCondition type="useAndReproduction">http://creativecommons.org/licenses/by-nc-sa/3.0/deed.es</mods:accessCondition>
<mods:subject>
<mods:topic>APOE polymorphisms</mods:topic>
</mods:subject>
<mods:subject>
<mods:topic>Type 2 diabetes mellitus glomerular filtration</mods:topic>
</mods:subject>
<mods:subject>
<mods:topic>Renal function</mods:topic>
</mods:subject>
<mods:titleInfo>
<mods:title>A common APOE polymorphism is an independent risk factor for reduced glomerular filtration rate in the Spanish RENASTUR cohort</mods:title>
</mods:titleInfo>
<mods:genre>postprint</mods:genre>
</mods:mods>
<?xml version="1.0" encoding="UTF-8" ?>
<atom:entry schemaLocation="http://www.w3.org/2005/Atom http://www.kbcafe.com/rss/atom.xsd.xml">
<atom:id>https://ria.asturias.es/RIA/handle/123456789/2741/ore.xml</atom:id>
<atom:published>2013-04-16T08:31:35Z</atom:published>
<atom:updated>2013-04-16T08:31:35Z</atom:updated>
<atom:source>
<atom:generator>RIA</atom:generator>
</atom:source>
<atom:title>A common APOE polymorphism is an independent risk factor for reduced glomerular filtration rate in the Spanish RENASTUR cohort</atom:title>
<atom:author>
<atom:name>Gómez, Juan</atom:name>
</atom:author>
<atom:author>
<atom:name>Tavira, Beatriz</atom:name>
</atom:author>
<atom:author>
<atom:name>Tranche, Salvador</atom:name>
</atom:author>
<atom:author>
<atom:name>Ortega, Francisco</atom:name>
</atom:author>
<atom:author>
<atom:name>Rodríguez, M. Isabel</atom:name>
</atom:author>
<atom:author>
<atom:name>Sánchez, Emilio</atom:name>
</atom:author>
<atom:author>
<atom:name>Marín, Rafael</atom:name>
</atom:author>
<atom:author>
<atom:name>Corao, Ana I.</atom:name>
</atom:author>
<atom:author>
<atom:name>Arenas, Jorge</atom:name>
</atom:author>
<atom:author>
<atom:name>Álvarez, Victoria</atom:name>
</atom:author>
<oreatom:triples>
<rdf:Description about="https://ria.asturias.es/RIA/handle/123456789/2741/ore.xml#atom">
<dcterms:modified>2013-04-16T08:31:35Z</dcterms:modified>
</rdf:Description>
<rdf:Description about="http://172.28.36.237:8080/jspui/bitstream/123456789/2741/1/Archivo.pdf">
<dcterms:description>ORIGINAL</dcterms:description>
</rdf:Description>
</oreatom:triples>
</atom:entry>
<?xml version="1.0" encoding="UTF-8" ?>
<qdc:qualifieddc schemaLocation="http://purl.org/dc/elements/1.1/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dc.xsd http://purl.org/dc/terms/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dcterms.xsd http://dspace.org/qualifieddc/ http://www.ukoln.ac.uk/metadata/dcmi/xmlschema/qualifieddc.xsd">
<dc:title>A common APOE polymorphism is an independent risk factor for reduced glomerular filtration rate in the Spanish RENASTUR cohort</dc:title>
<dc:creator>Gómez, Juan</dc:creator>
<dc:creator>Tavira, Beatriz</dc:creator>
<dc:creator>Tranche, Salvador</dc:creator>
<dc:creator>Ortega, Francisco</dc:creator>
<dc:creator>Rodríguez, M. Isabel</dc:creator>
<dc:creator>Sánchez, Emilio</dc:creator>
<dc:creator>Marín, Rafael</dc:creator>
<dc:creator>Corao, Ana I.</dc:creator>
<dc:creator>Arenas, Jorge</dc:creator>
<dc:creator>Álvarez, Victoria</dc:creator>
<dc:subject>APOE polymorphisms</dc:subject>
<dc:subject>Type 2 diabetes mellitus glomerular filtration</dc:subject>
<dc:subject>Renal function</dc:subject>
<dcterms:abstract>Objective. APOE gene variants may contribute to risk of chronic kidney disease. Our aim was to determine whether the common APOE-ε2/ε3/ε4 polymorphism was associated with reduced estimated glomerular filtration rate (eGFR) in the Renastur population, a cohort of elderly individuals from the region Asturias (Northern Spain). Methods. A total of 743 Spanish Caucasian aged 55-85 were genotyped for the APOE-ε2/ ε3/ ε4 polymorphisms. Individuals with a previous diagnostic of renal disease were not eligible for the study. Participants with a documented history of type 2 diabetes (T2DM) or hypertension or who were receiving antidiabetic or antihypertensive drugs were classified as diabetics and hypertensives. The eGFR was calculated with the Modification of Diet in Renal Disease formulae, and those with an eGFR <60 ml/min/1.73 m2 (n=91) were considered as having renal impaired function. The effect of alleles and genotypes on clinical (hypertension, diabetes) and analytical findings was statistically determined. Results. In addition to age and T2DM, APOE-ε2 was significantly associated with eGFR<60 (p=0.002; OR= 2.30). This association remained statistically significant after correction by multiple variants. Although the effect of the APOE-ε2 on eGFR was seen among diabetics and non diabetics, the significance was stronger in the T2DM group Conclusion. The APOE-ε2 allele was a genetic risk factor for impaired renal function among healthy Spanish elderly individuals.</dcterms:abstract>
<dcterms:dateAccepted>2013-04-16T08:31:35Z</dcterms:dateAccepted>
<dcterms:available>2013-04-16T08:31:35Z</dcterms:available>
<dcterms:created>2013-04-16T08:31:35Z</dcterms:created>
<dcterms:issued>2013</dcterms:issued>
<dc:type>postprint</dc:type>
<dc:identifier>https://ria.asturias.es/RIA/handle/123456789/2741</dc:identifier>
<dc:language>eng</dc:language>
<dc:relation>No, esta versión no ha sido citada</dc:relation>
<dc:rights>http://creativecommons.org/licenses/by-nc-sa/3.0/deed.es</dc:rights>
</qdc:qualifieddc>
<?xml version="1.0" encoding="UTF-8" ?>
<rdf:RDF schemaLocation="http://www.openarchives.org/OAI/2.0/rdf/ http://www.openarchives.org/OAI/2.0/rdf.xsd">
<ow:Publication about="oai:http://172.28.36.237/:123456789/2741">
<dc:title>A common APOE polymorphism is an independent risk factor for reduced glomerular filtration rate in the Spanish RENASTUR cohort</dc:title>
<dc:creator>Gómez, Juan</dc:creator>
<dc:creator>Tavira, Beatriz</dc:creator>
<dc:creator>Tranche, Salvador</dc:creator>
<dc:creator>Ortega, Francisco</dc:creator>
<dc:creator>Rodríguez, M. Isabel</dc:creator>
<dc:creator>Sánchez, Emilio</dc:creator>
<dc:creator>Marín, Rafael</dc:creator>
<dc:creator>Corao, Ana I.</dc:creator>
<dc:creator>Arenas, Jorge</dc:creator>
<dc:creator>Álvarez, Victoria</dc:creator>
<dc:subject>APOE polymorphisms</dc:subject>
<dc:subject>Type 2 diabetes mellitus glomerular filtration</dc:subject>
<dc:subject>Renal function</dc:subject>
<dc:description>Objective. APOE gene variants may contribute to risk of chronic kidney disease. Our aim was to determine whether the common APOE-ε2/ε3/ε4 polymorphism was associated with reduced estimated glomerular filtration rate (eGFR) in the Renastur population, a cohort of elderly individuals from the region Asturias (Northern Spain). Methods. A total of 743 Spanish Caucasian aged 55-85 were genotyped for the APOE-ε2/ ε3/ ε4 polymorphisms. Individuals with a previous diagnostic of renal disease were not eligible for the study. Participants with a documented history of type 2 diabetes (T2DM) or hypertension or who were receiving antidiabetic or antihypertensive drugs were classified as diabetics and hypertensives. The eGFR was calculated with the Modification of Diet in Renal Disease formulae, and those with an eGFR <60 ml/min/1.73 m2 (n=91) were considered as having renal impaired function. The effect of alleles and genotypes on clinical (hypertension, diabetes) and analytical findings was statistically determined. Results. In addition to age and T2DM, APOE-ε2 was significantly associated with eGFR<60 (p=0.002; OR= 2.30). This association remained statistically significant after correction by multiple variants. Although the effect of the APOE-ε2 on eGFR was seen among diabetics and non diabetics, the significance was stronger in the T2DM group Conclusion. The APOE-ε2 allele was a genetic risk factor for impaired renal function among healthy Spanish elderly individuals.</dc:description>
<dc:date>2013-04-16T08:31:35Z</dc:date>
<dc:date>2013-04-16T08:31:35Z</dc:date>
<dc:date>2013</dc:date>
<dc:type>postprint</dc:type>
<dc:identifier>https://ria.asturias.es/RIA/handle/123456789/2741</dc:identifier>
<dc:language>eng</dc:language>
<dc:relation>No, esta versión no ha sido citada</dc:relation>
<dc:rights>http://creativecommons.org/licenses/by-nc-sa/3.0/deed.es</dc:rights>
</ow:Publication>
</rdf:RDF>
<?xml version="1.0" encoding="UTF-8" ?>
<metadata schemaLocation="http://www.lyncode.com/xoai http://www.lyncode.com/xsd/xoai.xsd">
<element name="dc">
<element name="contributor">
<element name="author">
<element name="none">
<field name="value">Gómez, Juan</field>
<field name="value">Tavira, Beatriz</field>
<field name="value">Tranche, Salvador</field>
<field name="value">Ortega, Francisco</field>
<field name="value">Rodríguez, M. Isabel</field>
<field name="value">Sánchez, Emilio</field>
<field name="value">Marín, Rafael</field>
<field name="value">Corao, Ana I.</field>
<field name="value">Arenas, Jorge</field>
<field name="value">Álvarez, Victoria</field>
</element>
</element>
</element>
<element name="date">
<element name="accessioned">
<element name="none">
<field name="value">2013-04-16T08:31:35Z</field>
</element>
</element>
<element name="available">
<element name="none">
<field name="value">2013-04-16T08:31:35Z</field>
</element>
</element>
<element name="issued">
<element name="none">
<field name="value">2013</field>
</element>
</element>
</element>
<element name="identifier">
<element name="uri">
<element name="none">
<field name="value">https://ria.asturias.es/RIA/handle/123456789/2741</field>
</element>
</element>
</element>
<element name="description">
<element name="abstract">
<element name="eng">
<field name="value">Objective. APOE gene variants may contribute to risk of chronic kidney disease. Our aim was to determine whether the common APOE-ε2/ε3/ε4 polymorphism was associated with reduced estimated glomerular filtration rate (eGFR) in the Renastur population, a cohort of elderly individuals from the region Asturias (Northern Spain). Methods. A total of 743 Spanish Caucasian aged 55-85 were genotyped for the APOE-ε2/ ε3/ ε4 polymorphisms. Individuals with a previous diagnostic of renal disease were not eligible for the study. Participants with a documented history of type 2 diabetes (T2DM) or hypertension or who were receiving antidiabetic or antihypertensive drugs were classified as diabetics and hypertensives. The eGFR was calculated with the Modification of Diet in Renal Disease formulae, and those with an eGFR <60 ml/min/1.73 m2 (n=91) were considered as having renal impaired function. The effect of alleles and genotypes on clinical (hypertension, diabetes) and analytical findings was statistically determined. Results. In addition to age and T2DM, APOE-ε2 was significantly associated with eGFR<60 (p=0.002; OR= 2.30). This association remained statistically significant after correction by multiple variants. Although the effect of the APOE-ε2 on eGFR was seen among diabetics and non diabetics, the significance was stronger in the T2DM group Conclusion. The APOE-ε2 allele was a genetic risk factor for impaired renal function among healthy Spanish elderly individuals.</field>
</element>
</element>
<element name="sponsorship">
<element name="eng">
<field name="value">This work was supported by Red de Investigación Renal-REDINREN and Fondo de Investigaciones Sanitarias (grant 10/01971 to FO).</field>
</element>
</element>
</element>
<element name="language">
<element name="iso">
<element name="eng">
<field name="value">eng</field>
</element>
</element>
</element>
<element name="relation">
<element name="isreferencedby">
<element name="eng">
<field name="value">No, esta versión no ha sido citada</field>
</element>
</element>
</element>
<element name="rights">
<element name="eng">
<field name="value">http://creativecommons.org/licenses/by-nc-sa/3.0/deed.es</field>
</element>
</element>
<element name="subject">
<element name="eng">
<field name="value">APOE polymorphisms</field>
<field name="value">Type 2 diabetes mellitus glomerular filtration</field>
<field name="value">Renal function</field>
</element>
</element>
<element name="title">
<element name="eng">
<field name="value">A common APOE polymorphism is an independent risk factor for reduced glomerular filtration rate in the Spanish RENASTUR cohort</field>
</element>
</element>
<element name="type">
<element name="eng">
<field name="value">postprint</field>
</element>
</element>
</element>
<element name="bundles">
<element name="bundle">
<field name="name">ORIGINAL</field>
<element name="bitstreams">
<element name="bitstream">
<field name="name">Archivo.pdf</field>
<field name="originalName">Archivo.pdf</field>
<field name="format">application/pdf</field>
<field name="size">217928</field>
<field name="url">http://172.28.36.237:8080/jspui/bitstream/123456789/2741/1/Archivo.pdf</field>
<field name="checksum">dc3e800945716acf991a50bd1d82d8ca</field>
<field name="checksumAlgorithm">MD5</field>
<field name="sid">1</field>
</element>
</element>
</element>
</element>
<element name="others">
<field name="handle">123456789/2741</field>
<field name="identifier">oai:http://172.28.36.237/:123456789/2741</field>
<field name="lastModifyDate">2018-04-24 12:04:27.752</field>
</element>
<element name="repository">
<field name="name">RIA</field>
<field name="mail">gemma.gonzalez@ricoh.es</field>
</element>
</metadata>