Skip to main content
. Author manuscript; available in PMC: 2011 Aug 1.
Published in final edited form as: Gastroenterology. 2010 Apr 21;139(2):464–473.e3. doi: 10.1053/j.gastro.2010.04.042

Table 4.

Association of Haplotype Diversity with OS in All Patients

Haplotype* Frequency MST HR (95% CI) P
IGF2R
 ACAC 0.3287 18.7 1.0
 GTGC 0.0577 16.5 1.28 (1.00–1.64) 0.05
IGFBP3
 CGAT 0.3748 16.3 1.0
 ACAT 0.2825 17.7 0.87 (0.77–0.99) 0.04
IGFBP5
 CA 0.538 17.5 1.0
 TC 0.01 5.0 2.73 (1.02–7.34) 0.046
IRS1
 CGGG 0.8243 18.1 1.0
 CAGG 0.072 10.3 1.41 (1.13–1.76) 0.002
 GGGG 0.033 13.3 1.76 (1.28–2.42) <0.001
IRS2
 GACGTC 0.2399 18.5 1.0
 AGCGCT 0.0595 14.3 1.35 (1.02–1.77) 0.03
 GGCGTC 0.0439 14.7 1.43 (1.04–1.96) 0.03
 AGCGCC 0.0405 14.3 1.67 (1.21–2.29) 0.001

MST, median survival time (months); CI, confidence interval; HR: hazard ratio; CA19-9, carbohydrate antigen 19-9 HR values were from multivariate Cox regression models including sex, race, clinical stage, tumor resection, CA 19-9, biochemical index and performance status.

*

Haplotype of IGF2R T713T, L2222L, S350S, L252V; IGFBP3 -202A>C, A32G, H164P, Ex5-411A>T; IGFBP5 R138W, IVS1-6727A>C; IRS1 IVS1+4315C>G, G972R, IVS1-10949G>A, A512P; IRS2 Ex2+750A>G, G1057D, P829P, IVS1+2498G>A, IVS1+5687T>C, IVS1+166T>C. Those haplotypes with P>0.05 in Cox regression models were not shown.