TABLE 3.
Separate generalized logit regression models at all study visits to predict clinical outcome group statusa
| Characteristic | Unit increaseb | ORc (95% CI) |
|
|---|---|---|---|
| Return to health vs symptoms only | Return to health vs PTLDS | ||
| Acute phase, pretreatment | |||
| Fibrinogen | 443.74 ng/ml | 0.96 (0.65–1.44) | 0.78 (0.44–1.36) |
| MIG | 383.42 pg/ml | 0.91 (0.63–1.31) | 0.84 (0.35–2.02) |
| IP-10 | 509.06 pg/ml | 0.94 (0.67–1.32) | 0.85 (0.32–2.28) |
| CRPd | 57,140.56 ng/ml | 1.02 (0.68–1.53) | 1.57 (0.88–2.78) |
| Serum amyloid A | 3,173.89 ng/ml | 1.09 (0.78–1.51) | 1.11 (0.68–1.79) |
| Ferritin | 81,533.50 pg/ml | 0.86 (0.55–1.34) | 0.52 (0.15–1.82) |
| CCL19 | 78.81 pg/ml | 1.27 (0.87–1.85) | 1.36 (0.75–2.48) |
| Age | 1 yr | 1.01 (0.97–1.06) | 0.97 (0.90–1.03) |
| Sex | Female to male | 1.16 (0.33–4.15) | 0.32 (0.03–3.04) |
| Erythema migrans | Single to disseminated | 0.98 (0.28–3.36) | 0.30 (0.03–3.45) |
| Serology | Negative to positive | 1.12 (0.26–4.79) | 0.82 (0.12–5.67) |
| Posttreatment follow-up | |||
| CCL19 | 49.96 pg/ml | 1.49 (0.89–2.48) | 2.09 (1.12–3.88)e |
| Age | 1 year | 1.02 (0.98–1.06) | 0.98 (0.92–1.04) |
| Sex | Female to male | 0.96 (0.31–3.03) | 0.41 (0.06–2.97) |
| Presence of EM lesions | Single to disseminated | 0.85 (0.27–2.66) | 0.10 (0.01–1.96) |
| Serology | Negative to positive | 1.32 (0.38–4.60) | 0.72 (0.13–4.05) |
| 1-mo follow-up | |||
| CCL19 | 51.73 pg/ml | 1.47 (0.88–2.47) | 1.90 (1.06–3.39)e |
| Age | 1 year | 1.01 (0.97–1.05) | 0.96 (0.90–1.02) |
| Sex | Female to male | 1.05 (0.32–3.40) | 0.33 (0.05–2.26) |
| Presence of EM lesions | Single to disseminated | 0.86 (0.27–2.69) | 0.09 (0.01–2.33) |
| Serology | Negative to positive | 1.23 (0.33–4.60) | 0.48 (0.08–2.72) |
| 3-mo follow-up | |||
| CCL19 | 42.08 pg/ml | 1.20 (0.81–1.78) | 1.72 (1.03–2.88)e |
| Age | 1 year | 1.02 (0.98–1.06) | 0.98 (0.92–1.04) |
| Sex | Female to male | 1.07 (0.34–3.44) | 0.46 (0.06–3.43) |
| Presence of EM lesions | Single to disseminated | 0.89 (0.29–2.74) | 0.18 (0.01–2.24) |
| Serology | Negative to positive | 1.12 (0.32–3.87) | 0.52 (0.09–2.92) |
| 6 mo posttreatment | |||
| CCL19 | 30.99 pg/ml | 1.17 (0.82–1.67) | 1.84 (1.12–3.02)e |
| Age | 1 year | 1.02 (0.98–1.06) | 0.97 (0.91–1.03) |
| Sex | Female to male | 0.90 (0.29–2.75) | 0.26 (0.04–1.92) |
| Presence of EM lesions | Single to disseminated | 0.89 (0.28–2.83) | 0.10 (0.01–1.40) |
| Serology | Negative to positive | 1.34 (0.40–4.56) | 0.84 (0.15–4.72) |
| 1 yr posttreatment | |||
| CCL19 | 45.97 pg/ml | 1.03 (0.56–1.88) | 2.83 (1.15–6.94)e |
| Age | 1 year | 1.01 (0.97–1.05) | 0.98 (0.91–1.04) |
| Sex | Female to male | 0.77 (0.24–2.50) | 0.36 (0.04–3.57) |
| Presence of EM lesions | Single to disseminated | 1.07 (0.32–3.52) | 0.18 (0.01–2.30) |
| Serology | Negative to positive | 1.35 (0.37–4.97) | 1.17 (0.16–8.47) |
Clinical outcome group status (PTLDS, symptoms only, and return to health) was defined using a previously published definition incorporating both persistent symptoms and functional impact (25).
For immune markers, a unit increase was set at 0.5 SD for the Lyme disease participant sample.
OR, odds ratio.
CRP, C-reactive protein.
For significance of parameter estimate, P ≤ 0.05.