<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12</volume><submitter>Vimaleswaran KS</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Apolipoprotein (apo)B is the structural apoprotein of intestinally- and liver- derived lipoproteins and plays an important role in the transport of triacylglycerol (TAG) and cholesterol. Previous studies have examined the association between the APOB insertion/deletion (ins/del) polymorphism (rs17240441) and postprandial lipaemia in response to a single meal; however the findings have been inconsistent with studies often underpowered to detect genotype-lipaemia associations, focused mainly on men, or with limited postprandial characterisation of participants. In the present study, using a novel sequential test meal protocol which more closely mimics habitual eating patterns, we investigated the impact of APOB ins/del polymorphism on postprandial TAG, non-esterified fatty acids, glucose and insulin levels in healthy adults.&lt;h4>Findings&lt;/h4>Healthy participants (n = 147) consumed a standard test breakfast (0 min; 49 g fat) and lunch (330 min; 29 g fat), with blood samples collected before (fasting) and on 11 subsequent occasions until 480 min after the test breakfast. The ins/ins homozygotes had higher fasting total cholesterol, LDL-cholesterol, TAG, insulin and HOMA-IR and lower HDL-cholesterol than del/del homozygotes (P &lt; 0.017). A higher area under the time response curve (AUC) was evident for the postprandial TAG (P &lt; 0.001) and insulin (P = 0.032) responses in the ins/ins homozygotes relative to the del/del homozygotes, where the genotype explained 35% and 7% of the variation in the TAG and insulin AUCs, respectively.&lt;h4>Conclusions&lt;/h4>In summary, our findings indicate that the APOB ins/del polymorphism is likely to be an important genetic determinant of the large inter-individual variability in the postprandial TAG and insulin responses to dietary fat intake.</pubmed_abstract><journal>Nutrition &amp; metabolism</journal><pagination>7</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4365815</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The APOB insertion/deletion polymorphism (rs17240441) influences postprandial lipaemia in healthy adults.</pubmed_title><pmcid>PMC4365815</pmcid><pubmed_authors>Lovegrove JA</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Minihane AM</pubmed_authors><pubmed_authors>Vimaleswaran KS</pubmed_authors><pubmed_authors>Williams CM</pubmed_authors><pubmed_authors>Gill R</pubmed_authors><pubmed_authors>Jackson KG</pubmed_authors></additional><is_claimable>false</is_claimable><name>The APOB insertion/deletion polymorphism (rs17240441) influences postprandial lipaemia in healthy adults.</name><description>&lt;h4>Background&lt;/h4>Apolipoprotein (apo)B is the structural apoprotein of intestinally- and liver- derived lipoproteins and plays an important role in the transport of triacylglycerol (TAG) and cholesterol. Previous studies have examined the association between the APOB insertion/deletion (ins/del) polymorphism (rs17240441) and postprandial lipaemia in response to a single meal; however the findings have been inconsistent with studies often underpowered to detect genotype-lipaemia associations, focused mainly on men, or with limited postprandial characterisation of participants. In the present study, using a novel sequential test meal protocol which more closely mimics habitual eating patterns, we investigated the impact of APOB ins/del polymorphism on postprandial TAG, non-esterified fatty acids, glucose and insulin levels in healthy adults.&lt;h4>Findings&lt;/h4>Healthy participants (n = 147) consumed a standard test breakfast (0 min; 49 g fat) and lunch (330 min; 29 g fat), with blood samples collected before (fasting) and on 11 subsequent occasions until 480 min after the test breakfast. The ins/ins homozygotes had higher fasting total cholesterol, LDL-cholesterol, TAG, insulin and HOMA-IR and lower HDL-cholesterol than del/del homozygotes (P &lt; 0.017). A higher area under the time response curve (AUC) was evident for the postprandial TAG (P &lt; 0.001) and insulin (P = 0.032) responses in the ins/ins homozygotes relative to the del/del homozygotes, where the genotype explained 35% and 7% of the variation in the TAG and insulin AUCs, respectively.&lt;h4>Conclusions&lt;/h4>In summary, our findings indicate that the APOB ins/del polymorphism is likely to be an important genetic determinant of the large inter-individual variability in the postprandial TAG and insulin responses to dietary fat intake.</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015</publication><modification>2024-11-15T12:10:31.424Z</modification><creation>2019-06-06T14:08:42Z</creation></dates><accession>S-EPMC4365815</accession><cross_references><pubmed>25793007</pubmed><doi>10.1186/s12986-015-0002-9</doi></cross_references></HashMap>