<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9(2)</volume><submitter>Marrachelli VG</submitter><pubmed_abstract>To identify factors related with the risk to develop microalbuminuria using combined genomic and metabolomic values from a general population study. One thousand five hundred and two subjects, Caucasian, more than 18 years, representative of the general population, were included. Blood pressure measurement and albumin/creatinine ratio were measured in a urine sample. Using SNPlex, 1251 SNPs potentially associated to urinary albumin excretion (UAE) were analyzed. Serum metabolomic profile was assessed by 1H NMR spectra using a Brucker Advance DRX 600 spectrometer. From the total population, 1217 (mean age 54 ± 19, 50.6% men, ACR>30 mg/g in 81 subjects) with high genotyping call rate were analysed. A characteristic metabolomic profile, which included products from mitochondrial and extra mit</pubmed_abstract><journal>PloS one</journal><pagination>e98227</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4053470</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Genomic and metabolomic profile associated to microalbuminuria.</pubmed_title><pmcid>PMC4053470</pmcid><pubmed_authors>Mansego ML</pubmed_authors><pubmed_authors>Segura R</pubmed_authors><pubmed_authors>Chaves FJ</pubmed_authors><pubmed_authors>Galan I</pubmed_authors><pubmed_authors>Martin-Escudero JC</pubmed_authors><pubmed_authors>Marrachelli VG</pubmed_authors><pubmed_authors>Marin P</pubmed_authors><pubmed_authors>Lliso G</pubmed_authors><pubmed_authors>Morales JM</pubmed_authors><pubmed_authors>Briongos L</pubmed_authors><pubmed_authors>Redon J</pubmed_authors><pubmed_authors>Monleon D</pubmed_authors><pubmed_authors>Martinez F</pubmed_authors><pubmed_authors>Rentero P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Genomic and metabolomic profile associated to microalbuminuria.</name><description>To identify factors related with the risk to develop microalbuminuria using combined genomic and metabolomic values from a general population study. One thousand five hundred and two subjects, Caucasian, more than 18 years, representative of the general population, were included. Blood pressure measurement and albumin/creatinine ratio were measured in a urine sample. Using SNPlex, 1251 SNPs potentially associated to urinary albumin excretion (UAE) were analyzed. Serum metabolomic profile was assessed by 1H NMR spectra using a Brucker Advance DRX 600 spectrometer. From the total population, 1217 (mean age 54 ± 19, 50.6% men, ACR>30 mg/g in 81 subjects) with high genotyping call rate were analysed. A characteristic metabolomic profile, which included products from mitochondrial and extra mit</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014</publication><modification>2026-05-02T20:00:10.556Z</modification><creation>2019-03-26T23:26:12Z</creation></dates><accession>S-EPMC4053470</accession><cross_references><pubmed>24918908</pubmed><doi>10.1371/journal.pone.0098227</doi></cross_references></HashMap>