J. Thillet et al., ELEVATED LIPOPROTEIN(A) LEVELS AND SMALL APO(A) ISOFORMS ARE COMPATIBLE WITH LONGEVITY - EVIDENCE FROM A LARGE POPULATION OF FRENCH CENTENARIANS, Atherosclerosis, 136(2), 1998, pp. 389-394
Epidemiological studies have shown lipoprotein(a) (Lp(a)) to be an ind
ependent risk factor for cardiovascular disease. Lp(a) is a cholestero
l-rich, low-density lipoprotein (LDL)-like particle to which a large g
lycoprotein, apolipoprotein(a) (apo(a)) is attached. Plasma Lp(a) leve
ls are highly genetically determined and influenced to a minor degree
by environmental factors. In an effort to determine whether Lp(a) migh
t be associated with longevity, we have evaluated Lp(a) levels and apo
(a) isoform sizes in a population of French centenarians (n = 109) com
pared to a control group (n = 227). The mean age of centenarians was 1
01.5 +/- 2.4 years while the control group was 39.4 +/- 7.2 years. Pla
sma levels of total cholesterol and triglyceride were within the norma
l range in both centenarian and control subjects. Lp(a) levels were hi
gher in centenarians (both male and female) than in the normolipidemic
control group (mean Lp(a) level = 0.33 +/- 0.42 and 0.22 +/- 0.27 mg/
ml, respectively, P < 0.005). The distribution of apo(a) isoforms was
significantly shifted towards small isoform size in the centenarian po
pulation as compared to the controls (54.4 and 41.4% of isoforms less
than or equal to 27 kringles (kr), respectively, P = 0.04). Nonetheles
s, the apo(a) size distribution in centenarians did not entirely expla
in the high Lp(a) levels observed in this population. Factors other th
an apo(a) size, and which may be either genetic or environmental in na
ture, appear to contribute to the elevated plasma Lp(a) levels of our
centenarian population. We conclude therefore that high plasma Lp(a) l
evels are compatible with longevity. (C) 1998 Elsevier Science Ireland
Ltd.