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. 2014 May 10;36(3):9659. doi: 10.1007/s11357-014-9659-7

Table 1.

Necropsy results from the mouse longevity studies shown in Fig. 1

Organ Pathology Diet treatment (n)
Control (n = 36)a Lovaza (n = 35) Krill oil (n = 35)
No.b %c No. % P valued No. % P value
Spleen Enlarged/tumorous 23 63.9 23 65.7 1.0000 20 57.1 0.6312
Liver Tumor 11 30.6 17 48.6 0.1488 13 37.1 0.6210
Enlarged/fatty liver 1 2.8 1 2.9 1.0000 3 8.6 0.3570
Hemangioma 4 11.1 1 2.9 0.3570 0 0.0 0.1145
Intestinal Tumor 5 13.9 8 22.9 0.3723 4 11.4 1.0000
Lung Tumor 2 5.6 8 22.9 0.0457 16 45.7 9.769e-05
Penis Necrosed/inflamed 0 0 2 5.7 0.2394 0 0.0 1.0000
Seminal vesicles Enlarged 1 2.8 7 20.0 0.0278 3 8.6 0.3570
Bladder Distended 6 16.7 5 14.3 1.0000 2 5.7 0.2603
Kidneys Enlarged/tumorous 3 8.3 0 0.0 0.2394 2 5.7 1.0000
Thymus Enlarged 1 2.8 3 8.6 0.3570 4 11.4 0.1987
Skin/abdominal cavity Fibroma 1 2.8 1 2.9 1.0000 2 5.7 0.6142
Peritoneal cavity Hemorrhage 4 11.1 15 42.9 0.0032 12 34.3 0.0246

aNumber of necropsied mice in each treatment group. The necropsied control mice were chosen randomly from among the mice of appropriate ages for approximating the age distribution of the marine oil-treated mice. One mouse from each treatment group was cannibalized and could not be necropsied

bNumber of necropsied mice in each treatment group with the indicated pathologies

cPercent of the necropsied mice in the treatment group with the indicated pathologies

dFisher’s exact test was utilized to investigate the association between the pathologies and treatment groups. The values that were significantly different or near significance are in italics. The P values are two-sided