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. Author manuscript; available in PMC: 2014 May 20.
Published in final edited form as: Arterioscler Thromb Vasc Biol. 2004 Oct 28;25(1):204–210. doi: 10.1161/01.ATV.0000149146.32385.1b

Table 3.

Genotypic effect of the chromosome 4 QTL contributing to variations in metabolic syndrome-related phenotypes and atherosclerotic lesion area in [(PERAxB6-Ldlr−/−)F1 × B6-Ldlr−/−]N2 mice grouped by genotype at the peak linked marker, D4Mit143. Data are expressed as mean ± SD.

Genotype Lesion area (μm2/section) TG (mg/dl) BWTch(g) BWTWTD(g) Insulin (ng/ml) Leptin (ng/ml) Non HDL-C (mg/dl) HDL-C (mg/dl)
Males
BB (n=45) (21.7±10)×104 408±141 25.4±4 29.9±5 3.18±2 11.8±11 356±96 69±18
BP (n=30) (28.3±9)×104* 639±317 28.0±4* 33.3±5* 4.86±3 19.3±18§ 381±111 67±20
Females
BB (n=41) (32.7±11)×104 242±112 19.0±2 21.4±3 1.17±0.8 18.3±12 286±72 57±17
BP (n=51) (31.6±12)×104 348±266§ 20.5±2.8* 23.6±3.9* 1.03±0.9 26.1±15§ 351±128 53±17

BWTch, body weight after feeding a chow diet; BWTWTD, body weight after feeding a Western-type diet. All other traits were measured from mice fed a high fat Western-type diet. BB, homozygous for B6 alleles; BP, heterozygous for B6 and PERA/Ei alleles.

*

p ≤ 0.005 vs. BB

p <0.0001 vs. BB

p <0.009 vs. BB

§

p ≤ 0.03 vs. BB