Title | Lipoprotein lipase variants interact with polyunsaturated fatty acids for obesity traits in women: replication in two populations. |
Publication Type | Journal Article |
Year of Publication | 2014 |
Authors | Ma Y, Tucker KL, Smith CE, Lee YC, Huang T, Richardson K, Parnell LD, Lai CQ, Young KL, Justice AE, Shao Y, North KE |
Secondary Authors | Ordovás JM |
Journal | Nutr Metab Cardiovasc Dis |
Volume | 24 |
Issue | 12 |
Pagination | 1323-9 |
Date Published | 2014 Dec |
ISSN | 1590-3729 |
Keywords | Aged, Aged, 80 and over, Atherosclerosis, Body Mass Index, Boston, Diet, European Continental Ancestry Group, Fatty Acids, Unsaturated, Feeding Behavior, Female, Hispanic Americans, Humans, Indians, North American, Linkage Disequilibrium, Lipoprotein Lipase, Male, Middle Aged, Obesity, Polymorphism, Single Nucleotide |
Abstract | BACKGROUND AND AIMS: Lipoprotein lipase (LPL) is a candidate gene for obesity based on its role in triglyceride hydrolysis and the partitioning of fatty acids towards storage or oxidation. Whether dietary fatty acids modify LPL associated obesity risk is unknown. METHODS AND RESULTS: We examined five single nucleotide polymorphisms (SNPs) (rs320, rs2083637, rs17411031, rs13702, rs2197089) for potential interaction with dietary fatty acids for obesity traits in 1171 participants (333 men and 838 women, aged 45-75 y) of the Boston Puerto Rican Health Study (BPRHS). In women, SNP rs320 interacted with dietary polyunsaturated fatty acids (PUFA) for body mass index (BMI) (P = 0.002) and waist circumference (WC) (P = 0.001) respectively. Higher intake of PUFA was associated with lower BMI and WC in homozygotes of the major allele (TT) (P = 0.01 and 0.005) but not in minor allele carriers (TG and GG). These interactions were replicated in an independent population, African American women of the Atherosclerosis Risk in Communities (ARIC) study (n = 1334). CONCLUSION: Dietary PUFA modulated the association of LPL rs320 with obesity traits in two independent populations. These interactions may be relevant to the dietary management of obesity, particularly in women. |
DOI | 10.1016/j.numecd.2014.07.003 |
Alternate Journal | Nutr Metab Cardiovasc Dis |
PubMed ID | 25156894 |
PubMed Central ID | PMC4356006 |
Grant List | HHSN268201100012C / HL / NHLBI NIH HHS / United States P50 HL105185 / HL / NHLBI NIH HHS / United States P01 AG023394 / AG / NIA NIH HHS / United States HHSN268201100009I / HL / NHLBI NIH HHS / United States HHSN268201100010C / HL / NHLBI NIH HHS / United States HHSN268201100008C / HL / NHLBI NIH HHS / United States HHSN268201100005G / HL / NHLBI NIH HHS / United States HHSN268201100008I / HL / NHLBI NIH HHS / United States HHSN268201100007C / HL / NHLBI NIH HHS / United States P01AG023394 / AG / NIA NIH HHS / United States K08HL112845-01 / HL / NHLBI NIH HHS / United States HHSN268201100011I / HL / NHLBI NIH HHS / United States HHSN268201100011C / HL / NHLBI NIH HHS / United States R01 DK075681 / DK / NIDDK NIH HHS / United States HL54776 / HL / NHLBI NIH HHS / United States HHSN268201100006C / HL / NHLBI NIH HHS / United States HHSN268201100005I / HL / NHLBI NIH HHS / United States R01 DK089256 / DK / NIDDK NIH HHS / United States R01 DK075030 / DK / NIDDK NIH HHS / United States DK075030 / DK / NIDDK NIH HHS / United States HHSN268201100009C / HL / NHLBI NIH HHS / United States HHSN268201100005C / HL / NHLBI NIH HHS / United States HHSN268201100007I / HL / NHLBI NIH HHS / United States R01 HD057194 / HD / NICHD NIH HHS / United States L60 MD003562 / MD / NIMHD NIH HHS / United States T32 HL007055 / HL / NHLBI NIH HHS / United States R01 HL054776 / HL / NHLBI NIH HHS / United States K08 HL112845 / HL / NHLBI NIH HHS / United States |