Re-analysis of the North American
IgA Nephropathy Study suggested that efficacy of omega-3
polyunsaturated fatty acids (omega-3 PUFA) was dosage-dependent on the basis of body size and plasma omega-3/omega-6 and
eicosapentaenoic acid (EPA)/
arachidonic acid (AA) ratios. The objective of this study was to confirm these assertions. Data from a previously reported randomized 2-yr clinical trial in which two dosages of an ethyl
ester omega-3 PUFA (
Omacor) were given to 73 high-risk patients with
IgA nephropathy were reviewed.
Omacor also was used in the North American
IgA Nephropathy Study. Parameters included
body weight; body mass index (BMI); plasma
phospholipid AA, EPA, and docosahexanoic
acid (DHA) levels and serum
creatinine and 24-h urine
protein (UP) levels during the 2-yr trial; and time to
ESRD after 6.4 yr. Plasma
phospholipid levels of EPA, DHA, and EPA/AA ratios were significantly inversely correlated with increasing
body weight and BMI in the
Omacor 4-g dosage group but not in the
Omacor 8-g dosage group. Conversely, increasing levels of
lipid parameters were observed with increasing dosages of
Omacor (EPA+DHA) in grams per kilogram of
body weight at 6 wk of treatment. None of the plasma omega-3 PUFA levels, EPA/AA ratios, or
Omacor dosage per kilogram was significantly associated with reciprocal serum
creatinine or UP slopes during the 2-yr trial or with
ESRD. This post hoc analysis of
body weight and BMI, plasma omega-3 PUFA status, and renal outcome did not find that treatment efficacy of omega-3 PUFA was dosage dependent on the basis of body size.