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. 2013 Dec 29;4(2):123–142. doi: 10.1002/brb3.200

Table 4.

Multi-analyte regression models1

(a) Depression-Total (BDI-II)
Model fit F(1, 77) = 4.0145; P = 0.0487; R2 = 0.0502
Variable b t P
Intercept 1.8205 0.80 0.4284
HCV status 2.8974 2.00 0.0487
Model fit F(8, 77) = 4.787; P < 0.001; R2 = 0.3567
Variable b t P
Intercept 17.3226 4.20 <0.0001
HCV status 5.1596 3.23 0.0019
A2Macro −12.1283 −2.02 0.0475
BDNF −1.4825 −2.89 0.0052
Eotaxin1 −0.0165 −3.15 0.0024
IL23 4.7228 2.96 0.0042
RANTES 0.4548 1.99 0.0509
TNFα 2.6492 3.32 0.0015
TNFR2 −3.1421 −4.29 <0.0001
(b) Depression-Cognitive Affective Factor (BDI-II)
Model fit F(1, 77) = 1.364; P = 0.2466; R2 = 0.0176
Variable b t P
Intercept 0.0862 0.80 0.4241
HCV status 0.0793 1.17 0.2466
Model fit F(11, 77) = 4.0268; P < 0.0002; R2 = 0.4016
Variable b t P
Intercept 0.2661 1.35 0.1831
HCV status 0.1556 2.12 0.0375
AAT 0.4588 2.52 0.0143
BDNF −0.0731 −3.11 0.0028
Eotaxin1 −0.0005 −2.03 0.0465
IL15 −0.1373 −2.05 0.0441
IL18 −0.0011 −1.67 0.0997
IL23 0.2184 3.00 0.0039
RANTES 0.0221 2.10 0.0394
TNFα 0.1198 3.22 0.0020
TNFR2 −0.2101 −4.96 <0.0001
vWF 0.0088 1.93 0.0579
(c) Depression–Somatic Factor (BDI-II)
Model fit F(1/76) = 6.1293, P = 0.0156, R2 = 0.0756
Variable b t P
Intercept 0.1001 0.75 0.4559
HCV status 0.2082 2.48 0.0156
Model fit F(9/76) = 3.2644 P = 0.0024, R2 = 0.3048
Variable b t P
Intercept 1.0215 3.25 0.0018
HCV status 0.3342 3.49 0.0009
A2Macro −0.9127 −2.39 0.0196
C3 1.1813 1.75 0.0841
Fibrinogen −0.1525 −1.88 0.0649
IL23 0.2075 2.07 0.0426
IL8 0.0146 1.95 0.0558
MCP1 −0.0031 −2.56 0.0128
MIP1β −0.0020 −2.57 0.0123
MMP3 −0.0538 −2.14 0.0363
(d) Anxiety (GADI)
Model fit F(1, 76) = 5.4028; P < 0.0228; R2 = 0.0672
Variable b t P
Intercept 2.0202 0.65 0.5184
HCV status 4.5951 2.32 0.0228
Model fit F(5, 76) = 4.7444; P < 0.009; R2 = 0.2504
Variable b t P
Intercept 0.6811 0.17 0.8628
HCV status 4.9587 2.13 0.0370
MIP1α 0.1114 1.68 0.0966
SCF 0.0487 1.92 0.0589
TNFα 2.3309 1.98 0.0516
TNFR2 −3.1440 −3.20 0.0020
(e) Fatigue (FSS)
Model fit F(1, 75) = 9.0997; P < 0.035; R2 = 0.1095
Variable b t P
Intercept 1.6061 3.06 0.0030
HCV status 1.0000 3.02 0.0035
Model fit F(8, 75) = 4.3840; P < 0.0003; R2 = 0.3436
Variable b t P
Intercept 0.7798 0.78 0.4359
HCV status 0.5099 1.46 0.1485
AAT 2.1043 2.17 0.0335
BDNF −0.2359 −2.10 0.0396
FactorVII 0.0019 1.93 0.0583
IL7 0.1587 3.17 0.0023
RANTES 0.1255 2.38 0.0200
VDBP −0.0042 −1.99 0.0511
VEGF −0.0076 −2.11 0.0385
(f) Pain Severity (BPI-PS)
Model fit F(1, 76) = 1.4521; P < 0.2320; R2 = 0.0190
Variable b t P
Intercept 1.2919 1.55 0.1253
HCV status 0.6376 1.21 0.2320
Model fit F(5, 76) = 3.2423; P < 0.0108; R2 = 0.1859
Variable b t P
Intercept 0.9130 0.81 0.4195
HCV status 0.7797 1.47 0.1468
IL10 −0.2597 −1.82 0.0722
IL5 0.0642 2.26 0.0267
MIP1β −0.0111 −2.28 0.0255
SCF 0.0148 2.18 0.0325
(g) Pain Interference (BPI-PI)
Model fit F(1, 75) = 4.1609; P < 0.0449; R = 0.0532
Variable b t P
Intercept 0.2677 0.37 0.7155
HCV status 0.9513 2.04 0.0449
Model fit F(5, 75) = 3.5498; P < 0.0064; R2 = 0.2023
Variable b t P
Intercept 0.6042 0.71 0.4774
HCV status 1.0427 2.16 0.0338
CRP 0.2380 1.80 0.0755
IL10 −0.2695 −2.04 0.0456
MMP3 −0.3068 −2.19 0.0316
TNFα 0.5051 1.93 0.0574

BDI-II, Beck Depression Inventory-II; BPI-PI, Brief Pain Inventory-Pain Interference; BPI-PS, Brief Pain Inventory-Pain Severity; BDNF, brain-derived neurotrophic factor, CRP, C-reactive protein; DV, dependent variable; FSS, Fatigue Severity Scale; GADI, Generalized Anxiety Disorder Inventory; HCV+, adults with chronic hepatitis C virus infection; HCV−, Adults with no history of infection with the hepatitis C virus; MIP, macrophage inflammatory protein; RANTES, Regulated upon Activation, Normal T-cell Expressed, and Secreted; TNF, tumor necrosis factor; TNFR, Tumor Necrosis Factor Receptor 2; vWF, von Willebrand factor.

1

Regression models were developed in order to find which combination of plasma immune factors was significantly predictive of neuropsychiatric symptom severity on each of the seven neuropsychiatric variables within the total sample. Models were constructed with a backward selection linear regression of 33 immune factors. The backward selection started with the 33 immune factors and systematically eliminated from the model variables that were not significant, retaining only those with P-values (P ≤ 0.10). HCV Status was not allowed to be eliminated. Based on the final solution of the backward regression, a two-step model for each neuropsychiatric variable (DV) was constructed and these are presented above; fit parameters are presented as well as the unstandardized regression weights (b), t values and P-values for each immune factor. In these models, the first step consisted of regressing the DV onto HCV status (coded 0 for the HCV− control HCV Status, and 1 for the HCV+ HCV Status). In the second step, the significant immune factors from the backward selection were entered simultaneously with HCV status to create the final model. See Table 1 for immune factor abbreviations.

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