Table 5.
Factors |
Studies | Samples | Univariable analyses |
Multivariable analysis* |
||||||
---|---|---|---|---|---|---|---|---|---|---|
Total N |
Total n |
OR† (95% CI) |
P |
P‡ of LR test |
Variance explained R2 (%) |
AOR† (95% CI) |
P |
P§ of LR test |
||
Country/subregion:‖ | ||||||||||
Eastern MENA |
Afghanistan, Iran, Pakistan |
28 |
10 865 |
1.00 |
<0.001 |
31.52 |
1.00 |
<0.001 |
||
Egypt, Jordan, Yemen |
Egypt, Jordan, Yemen |
4 |
881 |
0.89 (0.15-5.10) |
0.893 |
0.66 (0.13-3.28) |
0.609 |
|||
North Africa |
Algeria, Morocco, Sudan, Tunisia |
48 |
12 394 |
5.34 (2.45-11.61) |
<0.001 |
5.01 (2.37-10.61) |
<0.001 |
|||
Horn of Africa |
Djibouti, Somalia, South Sudan |
26 |
5629 |
21.63 (8.89-52.69) |
<0.001 |
6.40 (2.45-16.69) |
<0.001 |
|||
Year of data collection¶ |
106 |
29 769 |
0.88 (0.85-0.91) |
<0.001 |
<0.001 |
34.61 |
0.93 (0.88-0.98) |
0.005 |
0.005 |
|
Infection type |
Current |
34 |
7103 |
1.00 |
0.515 |
0.00 |
– |
– |
– |
|
Ever** |
50 |
9968 |
1.25 (0.52-3.00) |
0.622 |
– |
– |
– |
|||
Unclear |
22 |
12 698 |
0.69 (0.23-2.04) |
0.501 |
– |
– |
– |
|||
Diagnostic method |
RPR/VDRL & TPHA/FTA-ABS/RDT |
29 |
6095 |
1.00 |
<0.001 |
22.44 |
1.00 |
0.444 |
||
RPR/VDRL |
4 |
488 |
0.09 (0.01-0.61) |
0.013 |
0.76 (0.15-4.00) |
0.746 |
||||
TPHA |
28 |
1781 |
2.17 (0.86-5.45) |
0.099 |
1.29 (0.54-3.07) |
0.558 |
||||
RDT |
23 |
8707 |
0.17 (0.06-0.45) |
<0.001 |
0.46 (0.18-1.18) |
0.104 |
||||
Not specified |
22 |
12 698 |
0.43 (0.16-1.16) |
0.094 |
0.75 (0.24-2.33) |
0.614 |
||||
STI ascertainment |
Biological assay not reported |
23 |
13 066 |
1.00 |
0.284 |
0.15 |
– |
– |
– |
|
Biological assay explicitly indicated |
83 |
16 703 |
1.66 (0.65-4.20) |
0.284 |
– |
– |
– |
|||
Sample size |
<100 participants |
42 |
1960 |
1.00 |
<0.001 |
20.02†† |
1.00 |
|||
≥100 participants |
64 |
27 809 |
0.16 (0.08-0.32) |
<0.001 |
1.60 (0.62-4.15) |
0.329 |
0.329 |
|||
Sampling methodology |
Non-probability/unclear sampling |
66 |
12 555 |
1.00 |
<0.001 |
18.73‡‡ |
1.00 |
|||
Probability-based sampling |
40 |
17 214 |
0.16 (0.08-0.34) |
<0.001 |
0.63 (0.25-1.63) |
0.339 |
0.339 |
|||
Response rate |
<60%/unclear |
69 |
18 400 |
1.00 |
<0.001 |
10.23§§ |
1.00 |
|||
≥60% | 37 | 11 369 | 0.25 (0.12-0.54) | 0.001 | 0.73 (0.29-1.84) | 0.495 | 0.495 |
AOR – adjusted odds ratio, CI – confidence interval, FTA-ABS – fluorescent treponemal antibody absorption test, LR – likelihood ratio, OR – odds ratio, P – P-value, RDT – rapid diagnostic test, RPR – rapid plasma regain, STI – sexually transmitted infection TPHA – Treponema pallidum haemagglutination assay. VDRL – venereal disease research laboratory
*Adjusted R2 in the multivariable model: 48.46%.
†An increment of 0.1 was added to number of events when generating log odds of syphilis infection. This is because 8 stratified measures had zero events.
‡Factors with P ≤ 0.1 were eligible for inclusion in the multivariable analysis.
§Factors with P < 0.05 in the multivariable model were considered as significant predictors.
‖Countries were grouped based on geography and similarity in prevalence levels.
¶Missing values for year of data collection (only one stratified measure) were imputed using data for year of publication adjusted by the median difference between year of publication and median year of data collection for studies with complete information.
**Ever infection indicates seropositivity using antibody testing.
††The high R2 was investigated and found to be due to confounding with year of data collection. Most studies with sample size ≥100 were conducted in recent years.
‡‡The high R2 was investigated and found to be due to confounding with country and year of data collection. Studies with non-probability sampling were mostly from the Horn of Africa. These studies tended also to be conducted in earlier years.
§§The high R2 was investigated and found to be due to confounding with year of data collection. Most studies with response rate ≥60% were conducted in recent years.