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Table 3 Cox regression analysisa of time to multiple clinical malaria episodesb between days 90 and 240

From: Immunoglobulin G subclass and antibody avidity responses in Malian children immunized with Plasmodium falciparum apical membrane antigen 1 vaccine candidate FMP2.1/AS02A

 

AMA1 vaccine group

Control group

No primary outcome episodes before day 90 (n = 66)

No primary outcome episodes before day 90 (n = 22)

Predictor variable

Hazard ratioc

P

Hazard ratio

P

log10 (IgG1 day 90)

1.17 [0.47, 2.93]

0.74

1.14 [0.65, 2.00]

0.66

log10 (IgG2 day 90)

0.92 [0.5, 1.70]

0.79

1.27 [0.43, 3.72]

0.66

log10 (IgG3 day 90)

1.89 [0.99, 3.61]

0.053

0.93 [0.35, 2.43]

0.87

log10 (IgG4 day 90)

1.06 [0.69, 1.63]

0.79

8.45 [0.61, 116.86]

0.11

log10 (cytophilic ratiod day 90)

0.83 [0.40, 1.70]

0.61

1.05 [0.44, 2.53]

0.91

  1. aGap time models with common regression coefficients using Firth’s penalized likelihood
  2. bClinical malaria episode defined using the primary outcome definition, i.e., an episode of malaria with axillary temperature of ≥ 37.5 °C and asexual P. falciparum density of ≥ 2500 parasites/mm3 of blood
  3. cHazard ratio and 95% confidence intervals for risk of multiple clinical malaria episodes after day 90
  4. dCytophilic ratio is the sum of IgG1 and IgG2 titers divided by the sum of the IgG3 and IgG4 titers