02700nas a2200337 4500000000100000008004100001260001200042653001000054653001400064653002100078653001700099653002000116653001400136100001300150700001400163700001400177700001400191700001300205700001400218700001600232700001400248700001800262700001500280700001900295245013200314856008300446300001100529490000700540520180100547022001402348 2026 d c03/202610aKenya10aDiagnosis10aDried blood spot10aEpidemiology10aschistosomiasis10aScreening1 aMiján A1 aMartín O1 aCiancas E1 aMartín C1 aLokoel G1 aLokaala S1 aLokiriama D1 aHernanz S1 ade Santiago M1 aBertomeu A1 aPerez-Molina J00aSchistosomiasis in Western Lake Turkana, Kenya: An Exploratory Serosurvey and Validation of Dried Blood Spots for Field Studies uhttps://pmc.ncbi.nlm.nih.gov/articles/PMC13119579/pdf/tropicalmed-11-00091.pdf a1 - 100 v113 a

BACKGROUND:

Schistosomiasis remains a significant neglected tropical disease in Kenya, but its presence in the western/northern Lake Turkana region is poorly characterised. We conducted an exploratory serosurvey to assess evidence of spp. exposure and a diagnostic accuracy study to evaluate dried blood spots (DBSs) for field serology.

METHODS:

We performed a cross-sectional survey in adults (≥18 years) from six communities in the western/northern and shoreline area of Turkana Lake, excluding individuals with >6 months of residence in other Kenyan endemic areas. Capillary blood was collected on DBSs and tested centrally using ELISA for spp. IgG. In parallel, DBS cards performance was compared with paired routine serum ELISA in 23 patients assessed for suspected schistosomiasis at our centre.

RESULTS:

We enrolled 155 participants (60% men; median age 30 years), with nearly universal reported freshwater contact (154/155, 99.4%). In the validation study, DBS values were lower than serum values (mean bias 0.27), with moderate correlation ( = 0.54) and modest discrimination (AUC 0.65; sensitivity 80% and specificity 50% at OD index >0.8). The median DBS ELISA OD index for the 155 participants was 0.55 (IQR, 0.34-0.79). Six samples exceeded 0.8, but these values were low, and all had negative IHA (<1/80), yielding no confirmed seropositive cases.

CONCLUSIONS:

These findings suggest low or absent sustained transmission in the sampled communities during the study period and indicate that DBS-based serology is operationally feasible but requires careful calibration and confirmatory testing for robust field inference.

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