TY - JOUR
T1 - Haptoglobin Genotype Is a Major Determinant of the Amount of Iron in the Human Atherosclerotic Plaque
AU - Moreno, Pedro R.
AU - Purushothaman, K. Raman
AU - Purushothaman, Meera
AU - Muntner, Paul
AU - Levy, Nina S.
AU - Fuster, Valentin
AU - Fallon, John T.
AU - Lento, Patrick A.
AU - Winterstern, Aaron
AU - Levy, Andrew P.
N1 - Funding Information:
This work was supported by grants from the Israel Science Foundation, U.S.-Israel Binational Science Foundation, and the Kennedy Leigh Trust (to Dr. Levy) and by the Mount Sinai Hospital Norman Levy Foundation. Dr. Levy is a consultant for Synvista Therapeutics.
PY - 2008/9/23
Y1 - 2008/9/23
N2 - Objectives: We sought to test the hypothesis that haptoglobin (Hp) genotype is a determinant of the amount of iron in the atherosclerotic plaque. Background: In atherosclerotic lesions, intraplaque hemorrhage releases free hemoglobin (Hb), whose incorporated iron can act as an oxidant and inflammatory stimulus. These effects are antagonized by Hp, which binds free Hb and facilitates its clearance from the plaque. The Hp gene has 2 alleles (1 and 2), giving rise to 3 genotypes: Hp 1-1, Hp 2-1, and Hp 2-2. We previously hypothesized that Hp 2-2 individuals with diabetes mellitus (DM) have impaired clearance of Hb and its iron cargo from the plaque. Methods: We identified the presence or absence of Perl's iron stain in 189 plaques obtained from 37 decedents at autopsy. Results: Among DM, the prevalence of Perl's iron stain was increased in Hp 2-2 compared with that seen in Hp 1-1 or 2-1 (46.2% vs. 11.8%). After accounting for the within-decedent correlation of plaques, the prevalence ratio of Perl's iron stain associated with Hp 2-2 was 3.97 (95% confidence interval: 1.38 to 11.5; p = 0.025). In non-DM plaques, there was a nonsignificant trend towards a higher prevalence of iron staining in Hp 2-2 compared with that in Hp 1-1 or 2-1 (26.8% vs. 11.1%; prevalence ratio =2.40 [95% confidence interval: 0.81 to 7.09]; p = 0.114). Conclusions: These data support an impaired clearance of Hb from plaques in Hp 2-2 individuals, particularly in DM. The higher prevalence of plaque iron in Hp 2-2 DM individuals may contribute to the increased incidence of atherothrombotic events in these patients.
AB - Objectives: We sought to test the hypothesis that haptoglobin (Hp) genotype is a determinant of the amount of iron in the atherosclerotic plaque. Background: In atherosclerotic lesions, intraplaque hemorrhage releases free hemoglobin (Hb), whose incorporated iron can act as an oxidant and inflammatory stimulus. These effects are antagonized by Hp, which binds free Hb and facilitates its clearance from the plaque. The Hp gene has 2 alleles (1 and 2), giving rise to 3 genotypes: Hp 1-1, Hp 2-1, and Hp 2-2. We previously hypothesized that Hp 2-2 individuals with diabetes mellitus (DM) have impaired clearance of Hb and its iron cargo from the plaque. Methods: We identified the presence or absence of Perl's iron stain in 189 plaques obtained from 37 decedents at autopsy. Results: Among DM, the prevalence of Perl's iron stain was increased in Hp 2-2 compared with that seen in Hp 1-1 or 2-1 (46.2% vs. 11.8%). After accounting for the within-decedent correlation of plaques, the prevalence ratio of Perl's iron stain associated with Hp 2-2 was 3.97 (95% confidence interval: 1.38 to 11.5; p = 0.025). In non-DM plaques, there was a nonsignificant trend towards a higher prevalence of iron staining in Hp 2-2 compared with that in Hp 1-1 or 2-1 (26.8% vs. 11.1%; prevalence ratio =2.40 [95% confidence interval: 0.81 to 7.09]; p = 0.114). Conclusions: These data support an impaired clearance of Hb from plaques in Hp 2-2 individuals, particularly in DM. The higher prevalence of plaque iron in Hp 2-2 DM individuals may contribute to the increased incidence of atherothrombotic events in these patients.
KW - atherosclerotic plaque
KW - diabetes mellitus
KW - intraplaque hemorrhage
KW - iron
UR - http://www.scopus.com/inward/record.url?scp=51449122325&partnerID=8YFLogxK
U2 - 10.1016/j.jacc.2008.06.029
DO - 10.1016/j.jacc.2008.06.029
M3 - Article
C2 - 18848136
AN - SCOPUS:51449122325
SN - 0735-1097
VL - 52
SP - 1049
EP - 1051
JO - Journal of the American College of Cardiology
JF - Journal of the American College of Cardiology
IS - 13
ER -