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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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Staphylococcus aureus Carriage in Hidradenitis Suppurativa: Impact on Response to Adalimumab

Thumbnail
Συγγραφέας
Stergianou D., Tzanetakou V., Argyropoulou M., Kanni T., Bagos P.G., Giamarellos-Bourboulis E.J.
Ημερομηνία
2021
Γλώσσα
en
DOI
10.1159/000512617
Λέξη-κλειδί
adalimumab
amoxicillin plus clavulanic acid
clindamycin
cloxacillin
meticillin
moxifloxacin
adalimumab
antiinflammatory agent
adult
antibiotic sensitivity
antibiotic therapy
Article
bacterial colonization
bacterium culture
clinical article
cohort analysis
controlled study
disease classification
disease severity
drug withdrawal
exploratory research
female
follow up
Hidradenitis Suppurativa Clinical Response score
human
Hurley stage
incidence
inflammation
male
nose
nose smear
observational study
priority journal
recurrent disease
retrospective study
skin abscess
skin disease assessment
skin nodule
Staphylococcus aureus
Staphylococcus aureus infection
suppurative hidradenitis
treatment response
unspecified side effect
epidemiology
heterozygote
isolation and purification
microbiology
middle aged
nose cavity
Staphylococcus aureus
suppurative hidradenitis
young adult
Adalimumab
Adult
Anti-Inflammatory Agents
Carrier State
Female
Hidradenitis Suppurativa
Humans
Incidence
Male
Middle Aged
Nasal Cavity
Retrospective Studies
Staphylococcus aureus
Young Adult
S. Karger AG
Εμφάνιση Μεταδεδομένων
Επιτομή
Background: Several patients with hidradenitis suppurativa (HS) present flare-ups during treatment with adalimumab (ADA), the cause of which is not clear. ADA is the only FDA-approved biologic for the therapy of moderate-to-severe HS. A previous study of our group has shown that Staphylococcus aureus stimulation of whole blood affects the production of human β-defensin 2 and modulates HS severity. It is, therefore, hypothesized, that carriage of S. aureus may drive HS flare-ups. Objective: To explore the association between carriage of S. aureus and loss of response to ADA. Patients and Methods: Among patients with moderate-to-severe HS without carriage of S. aureus at start of treatment with ADA, we investigated for carriage of S. aureus from the nares when flare-ups occurred. Flare-ups were pre-defined as at least 25% increase of inflammatory lesions (sum of inflammatory nodules and abscesses) from baseline. Samplings were also done after completion of 12 weeks of ADA treatment from all patients who did not present flare-ups. Clinical response to ADA was assessed by the HS Clinical Response score (HiSCR). Results: Thirty-nine patients were studied; 24 with Hurley II stage HS and 15 with Hurley III stage HS. Twenty-nine patients achieved HiSCR after 12 weeks of treatment without any flare-ups; 10 patients had flare-ups and failed HiSCR. Three (10.3%) and 5 (50%) patients, respectively, had nasal carriage of S. aureus (odds ratio 8.67; 95% CI 1.54-48.49; p = 0.014). Among 32 patients reaching follow-up week 48, 20 patients achieved HiSCR and 12 had flare-ups leading to ADA failure; 2 (10%) and 5 (41.7%) patients, respectively, had positive culture for S. aureus (odds ratio 6.42; 95% CI 1.00-41.20; p = 0.05). Conclusion: Nasal carriage of S. aureus may be associated with loss of response to ADA. Findings need confirmation in larger series of patients. © 2021
URI
http://hdl.handle.net/11615/79468
Collections
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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