Doxycycline improves filarial lymphedema independent of active filarial infection: a randomized controlled trial

Sabine Mand, Alexander Yaw Debrah, Ute Klarmann, Linda Batsa, Yeboah Marfo-Debrekyei, Alexander Kwarteng, Sabine Specht, Aurea Belda-Domene, Rolf Fimmers, Mark Taylor, Ohene Adjei, Achim Hoerauf

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93 Citations (Scopus)

Abstract

BACKGROUND

The aim of this study was to determine whether improvement of filarial lymphedema (LE) by doxycycline is restricted to patients with ongoing infection (positive for circulating filarial antigen [CFA]), or whether the majority of CFA-negative patients with LE would also show a reduction in LE severity.

METHODS

One hundred sixty-two Ghanaian participants with LE stage 1-5 (Dreyer) were randomized blockwise into 2 groups (CFA positive or negative) and allocated to 3 treatment arms of 6 weeks: (1) amoxicillin (1000 mg/d), (2) doxycycline (200 mg/d), or (3) placebo matching doxycycline. All groups received standard hygiene morbidity management. The primary outcome was reduction of LE stages. Secondary outcomes included frequency of acute attacks and ultrasonographic assessment of skin thickness at the ankles. Parameters were assessed before treatment and after 3, 12, and 24 months.

RESULTS

Doxycycline-treated patients with LE stage 2-3 showed significant reductions in LE severity after 12 and 24 months, regardless of CFA status. Improvement was observed in 43.9% of doxycycline-treated patients, compared with only 3.2% and 5.6% in the amoxicillin and placebo arms, respectively. Skin thickness was correlated with LE stage improvement. Both doxycycline and amoxicillin were able to reduce acute dermatolymphangioadenitis attacks.

CONCLUSIONS

Doxycycline treatment improves mild to moderate LE independent of ongoing infection. This finding expands the benefits of doxycycline to the entire population of patients suffering from LE. Patients with LE stage 1-3 should benefit from a 6-week course of doxycycline every other year or yearly, which should be considered as an improved tool to manage morbidity in filarial LE.

Original languageEnglish
Pages (from-to)621-630
Number of pages10
JournalClinical Infectious Diseases
Volume55
Issue number5
DOIs
Publication statusPublished - 18 May 2012

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