TY - JOUR
T1 - Pentanucleotide repeat polymorphism, lipoprotein(a) levels, and risk of ischemic heart disease
AU - Kamstrup, Pia R
AU - Tybjaerg-Hansen, Anne
AU - Steffensen, Rolf
AU - Nordestgaard, Børge G
PY - 2008/10
Y1 - 2008/10
N2 - CONTEXT: Lipoprotein(a) is a cardiovascular risk factor. Levels of lipoprotein(a) are predominantly determined by apolipoprotein(a) gene variation, including a pentanucleotide repeat promoter polymorphism.OBJECTIVE: We tested the hypothesis that apolipoprotein(a) pentanucleotide repeat genotype predicts elevated lipoprotein(a) levels and risk of myocardial infarction (MI) and ischemic heart disease (IHD) in the general population.DESIGN: We used a cohort study of the Danish general population, The Copenhagen City Heart Study, including 10,276 individuals of which 860 and 1,781 developed MI and IHD, respectively, during up to 31 yr of follow-up, and a case-control study including 1,814 IHD patients and 5,076 controls. Follow-up was 100% complete.RESULTS: Allele frequencies were 0.0018, 0.0018, 0.6750, 0.1596, 0.1465, 0.0146, and 0.0004 for 6, 7, 8, 9, 10, 11, and 12 repeats, respectively. Mean lipoprotein(a) levels were 40, 36, and 27 mg/dl for individuals with 14-15, 16, and 17-22 repeats (sum of repeats on both alleles), respectively (trend, P < 0.001). Cumulative incidence of MI and IHD was increased for individuals with 14-15 vs. at least 16 repeats (log rank, P < 0.001 and P = 0.002). Multifactorially adjusted hazard ratios for 14-15 and 17-22 vs. 16 repeats were 3.1 (95% confidence interval, 1.6-5.8) and 1.0 (0.9-1.2) for MI and 2.2 (1.3-3.6) and 1.0 (0.9-1.1) for IHD. In the case-control study, multifactorially adjusted odds ratios for 14-15 and 17-22 vs. 16 repeats were 2.9 (1.1-7.8) and 0.9 (0.8-1.0) for MI and 2.5 (1.0-6.0) and 0.9 (0.8-1.0) for IHD.CONCLUSIONS: Apolipoprotein(a) 14-15 pentanucleotide repeats predict elevated levels of lipoprotein(a) and a 3- and 2-fold increased risk of MI and IHD in the general population.
AB - CONTEXT: Lipoprotein(a) is a cardiovascular risk factor. Levels of lipoprotein(a) are predominantly determined by apolipoprotein(a) gene variation, including a pentanucleotide repeat promoter polymorphism.OBJECTIVE: We tested the hypothesis that apolipoprotein(a) pentanucleotide repeat genotype predicts elevated lipoprotein(a) levels and risk of myocardial infarction (MI) and ischemic heart disease (IHD) in the general population.DESIGN: We used a cohort study of the Danish general population, The Copenhagen City Heart Study, including 10,276 individuals of which 860 and 1,781 developed MI and IHD, respectively, during up to 31 yr of follow-up, and a case-control study including 1,814 IHD patients and 5,076 controls. Follow-up was 100% complete.RESULTS: Allele frequencies were 0.0018, 0.0018, 0.6750, 0.1596, 0.1465, 0.0146, and 0.0004 for 6, 7, 8, 9, 10, 11, and 12 repeats, respectively. Mean lipoprotein(a) levels were 40, 36, and 27 mg/dl for individuals with 14-15, 16, and 17-22 repeats (sum of repeats on both alleles), respectively (trend, P < 0.001). Cumulative incidence of MI and IHD was increased for individuals with 14-15 vs. at least 16 repeats (log rank, P < 0.001 and P = 0.002). Multifactorially adjusted hazard ratios for 14-15 and 17-22 vs. 16 repeats were 3.1 (95% confidence interval, 1.6-5.8) and 1.0 (0.9-1.2) for MI and 2.2 (1.3-3.6) and 1.0 (0.9-1.1) for IHD. In the case-control study, multifactorially adjusted odds ratios for 14-15 and 17-22 vs. 16 repeats were 2.9 (1.1-7.8) and 0.9 (0.8-1.0) for MI and 2.5 (1.0-6.0) and 0.9 (0.8-1.0) for IHD.CONCLUSIONS: Apolipoprotein(a) 14-15 pentanucleotide repeats predict elevated levels of lipoprotein(a) and a 3- and 2-fold increased risk of MI and IHD in the general population.
KW - Adult
KW - Case-Control Studies
KW - Cohort Studies
KW - Female
KW - Follow-Up Studies
KW - Gene Frequency
KW - Genetic Predisposition to Disease
KW - Humans
KW - Incidence
KW - Lipoprotein(a)/blood
KW - Male
KW - Microsatellite Repeats/physiology
KW - Middle Aged
KW - Myocardial Infarction/epidemiology
KW - Myocardial Ischemia/blood
KW - Polymorphism, Genetic/physiology
KW - Risk Factors
U2 - 10.1210/jc.2008-0830
DO - 10.1210/jc.2008-0830
M3 - Journal article
C2 - 18682504
SN - 0021-972X
VL - 93
SP - 3769
EP - 3776
JO - The Journal of clinical endocrinology and metabolism
JF - The Journal of clinical endocrinology and metabolism
IS - 10
ER -