<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Demarco VG</submitter><funding>NIA NIH HHS</funding><funding>NHLBI NIH HHS</funding><pagination>159-71</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3529378</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>154(1)</volume><pubmed_abstract>Obesity and a nondipping circadian blood pressure (BP) pattern are associated with diastolic dysfunction. Ectopic lipid accumulation is increasingly recognized as an important metabolic abnormality contributing to diastolic dysfunction. However, little is known about the contribution of different lipids and the composition of lipid analytes to diastolic dysfunction. We have performed functional and structural studies and analyzed cardiac lipid profile at two time points during progression to diastolic dysfunction in a genetic model of obesity. Serial cardiac magnetic resonance imaging and telemetric measures of BP between 12 and 15 wk of age in obese male db/db mice indicated a nondipping circadian BP pattern and normal diastolic function at 12 wk that progressed to a deteriorating nondipp</pubmed_abstract><journal>Endocrinology</journal><pubmed_title>Obesity-related alterations in cardiac lipid profile and nondipping blood pressure pattern during transition to diastolic dysfunction in male db/db mice.</pubmed_title><pmcid>PMC3529378</pmcid><funding_grant_id>R01 HL074214</funding_grant_id><funding_grant_id>R21 HL111906</funding_grant_id><funding_grant_id>AG040638</funding_grant_id><funding_grant_id>HL-074214</funding_grant_id><funding_grant_id>R03 AG040638</funding_grant_id><funding_grant_id>HL-73101</funding_grant_id><funding_grant_id>HL107910</funding_grant_id><funding_grant_id>R01 HL073101</funding_grant_id><funding_grant_id>R01 HL107910</funding_grant_id><funding_grant_id>HL-111906</funding_grant_id><pubmed_authors>Albert CJ</pubmed_authors><pubmed_authors>Henriksen EJ</pubmed_authors><pubmed_authors>Lally JW</pubmed_authors><pubmed_authors>Demarco VG</pubmed_authors><pubmed_authors>Ma L</pubmed_authors><pubmed_authors>Johnson MS</pubmed_authors><pubmed_authors>Yang M</pubmed_authors><pubmed_authors>Whaley-Connell AT</pubmed_authors><pubmed_authors>Ford DA</pubmed_authors><pubmed_authors>Habibi J</pubmed_authors><pubmed_authors>Ford CA</pubmed_authors><pubmed_authors>Hayden MR</pubmed_authors><pubmed_authors>Sowers JR</pubmed_authors><pubmed_authors>Prasannarong M</pubmed_authors><pubmed_authors>Aroor AR</pubmed_authors></additional><is_claimable>false</is_claimable><name>Obesity-related alterations in cardiac lipid profile and nondipping blood pressure pattern during transition to diastolic dysfunction in male db/db mice.</name><description>Obesity and a nondipping circadian blood pressure (BP) pattern are associated with diastolic dysfunction. Ectopic lipid accumulation is increasingly recognized as an important metabolic abnormality contributing to diastolic dysfunction. However, little is known about the contribution of different lipids and the composition of lipid analytes to diastolic dysfunction. We have performed functional and structural studies and analyzed cardiac lipid profile at two time points during progression to diastolic dysfunction in a genetic model of obesity. Serial cardiac magnetic resonance imaging and telemetric measures of BP between 12 and 15 wk of age in obese male db/db mice indicated a nondipping circadian BP pattern and normal diastolic function at 12 wk that progressed to a deteriorating nondipp</description><dates><release>2013-01-01T00:00:00Z</release><publication>2013 Jan</publication><modification>2025-05-18T11:57:57.224Z</modification><creation>2025-05-18T11:57:57.224Z</creation></dates><accession>S-EPMC3529378</accession><cross_references><pubmed>23142808</pubmed><doi>10.1210/en.2012-1835</doi></cross_references></HashMap>