Table 1 |
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|
The characteristics of the study cohort in the S. haematobium and HIV-1 co-infection |
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|
Variable |
n |
Median MIP-1α/CCL3 (pg/ml) |
(Interquartile range) |
p-value |
|
|
||||
|
Sex |
||||
|
Male |
76 |
144 |
(65 - 295) |
|
|
Female |
303 |
127 |
(56 - 205) |
0.2130 |
|
Total |
379 |
|||
|
|
||||
|
S. haematobium |
||||
|
Positive |
263 |
171 |
(132 - 630) |
|
|
Negative |
116 |
39 |
(4 - 90) |
0.0029 |
|
|
||||
|
HIV status |
||||
|
Positive |
198 |
124 |
(36 - 550) |
|
|
Negative |
181 |
139 |
(47 - 445) |
0.6312 |
|
|
||||
|
Age (years) |
||||
|
< 25 |
82 |
166 |
(55 - 525) |
|
|
≥ 25 |
297 |
121 |
(35 - 595) |
0.2570 |
|
|
||||
|
Age groups (years) |
||||
|
< 20 |
24 |
146 |
(66 - 378) |
|
|
20 - 29 |
156 |
135 |
(78 - 402) |
|
|
30 - 39 |
92 |
113 |
(46 - 399) |
|
|
40 - 49 |
76 |
126 |
(72 - 332) |
|
|
50 + |
31 |
163 |
(33 - 298) |
0.5060 |
|
|
||||
|
Co-infection status |
||||
|
HIV+ S. haematobium + |
154 |
144 |
(124 - 447) |
|
|
HIV- S. haematobium + |
130 |
177 |
(133 - 506) |
|
|
HIV+ S. haematobium - |
48 |
64 |
(6 - 79) |
|
|
HIV- S. haematobium - |
47 |
30 |
(3 - 57) |
0.0008 |
|
|
||||
|
CD4 vs MIP-1a/CCL3 in HIV+ |
||||
|
Above 250 |
180 |
120 |
(38 - 440) |
|
|
Below 250 |
18 |
156 |
(36 - 398) |
0.4993 |
|
|
||||
|
Eggs per 10 ml urine |
||||
|
0 |
116 |
36 |
(5 - 81) |
|
|
<10 |
177 |
80 |
(66 - 168) |
|
|
10 - <50 |
77 |
379 |
(211 - 680) |
|
|
>50 |
9 |
333 |
(199 - 862) |
0.0001 |
|
|
||||
|
Time point |
||||
|
Baseline (before treatment) |
263 |
131 |
(102 - 560) |
|
|
3 months post treatment |
83 |
71 |
(6 - 94) |
0.0001 |
|
|
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|
Given are the medians and interquartile ranges of levels of plasma MIP-1α/CCL3 chemokine. The MIP-1α/CCL3 was measured in pg/ml using double sandwich ELISA within the range 15 pg/ml - 2000 pg/ml. Results from egg counts were used to stratify the schistosomiasis status of the participants into subgroups (no schistosomiasis, infection with S. haematobium only and co-infection with HIV-1. HIV-1 status and schistosomiasis status as classifying variables was used to identify differences between groups with respect to egg counts, age, and MIP-1α/CCL3; and p < 0.05 was considered to be significant. |
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|
Zinyama-Gutsire et al. BMC Infectious Diseases 2009 9:174 doi:10.1186/1471-2334-9-174 |
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