A. D'Arienzo

G. De Franchis

G. Valente

M. Rea

M. Sanges

R. Della Gatta

R. Sollazzo

D'ARIENZO, AGESILAO

Archivio della ricerca - Università degli studi di Napoli Federico II

Dear Editor, ulcerative colitis (UC) is an inflammatory bowel disease associated with a variety of ex-traintestinal manifestations (EIMs) that may produce greater morbidity than the underlying in-testinal disease and may even be the initial presenting symptoms. An arthritis affecting thespine and/or peripheral joints has been considered the most common EIM of UC. It is charac-terized by the absence of serum rheumatoid factor, the peripheral and axial form occurring inabout 10-23% and about 10-15%, respectively1-3. Articular and musculoskeletal manifestationsin UC patients are included in the spondyloarthropathies (SpAs) that are a group of seronega-tive autoimmune related disorders with common characteristics including: ankylosing spondyli-tis, reactive arthritis, psoriatic arthritis, inflammatory bowel disease, some forms of juvenilearthritis and acute anterior uveitis4.Evidence coming from many studies in genetically susceptible animal models of colitis sug-gests the crucial role of enteric flora in activating the immune system against bacterial antigensand contemporary against colonic mucosa on the basis of an antigenic cross-reactivity (“antigenmimicry”). The sharing of these colonic antigens by joints, associated with a genetic susceptibility,would lead to an immune attack against these sites5,6. Several studies in animal models of experi-mental arthritis have demonstrated the beneficial effects of probiotics, in particular Lactobacillusspecies, on articular inflammation7-10. Preliminary results suggest that a probiotic mixture (VSL#3)may be an alternative treatment for arthralgia in patients with inflammatory bowel dis-ease11. Nevertheless, a recent internet-based randomized controlled trial in patients with SpA hasshowed no statistical or clinical significant improvement with the use of probiotics12.We performed an open-label, non-controlled study to determine if an association of probi-otics, Lactobacillus Acidophilus (LA) and Lactobacillus Salivarius (LS), could improve SpA in pa-tients with quiescent UC. Eighteen patients (10:8=F:M, mean age 49 years) with quiescent UCand active SpA received an open label association of LA and LS, two billions bacteria daily intwo divided doses for four weeks. The clinical parameters evaluated included Bath AnkylosingSpondylitis Disease Activity Index (BASDAI), assessing disease activity, Bath AnkylosingSpondylitis Functional Index (BASFI), assessing patientʼs functional limitations and visual ana-logue scale (VAS), assessing subjective pain perception. Laboratory parameters evaluated in-cluded C-reactive protein (CRP) and erythrocyte sedimentation rate (ESR). CRP was measuredby a highly sensitive turbidimetric method (normal value <5 mg/L). ESR was assessed using aquantitative capillary photometry-based technology. At baseline and at the end of the studymean ± standard deviation (SD) values were calculated. Data were analyzed using Studentʼs t-test (p<0.05 was considered significant). At baseline UC was quiescent according to UC Dis-ease Activity Index (UCDAI), activity of SpA was documented by BASDAI score ≥4.At the end of the study a significant reduction of BASDAI score (5.8 ± 1.5 vs 4 ± 1.8,p<0.05) and VAS score (58.1 ± 16.8 vs 41.5 ± 14.3, p<0.05) was seen. No significant reduc-tion of BASFI score (33.6 ± 10 vs 28.6 ± 6.3, p=0.08), CRP (25.2 ± 11 vs 19.8 ± 6.4, p=0.08)and ESR (28 ± 11.6 vs 22.5 ± 7.1, p= 0.1) was evidenced (Table I). During the study no one ofthe patients had a relapse of UC or relevant adverse effects.European Review for Medical and Pharmacological Sciences 2009; 13: 233-234Probiotics in spondyloarthropathyassociated with ulcerative colitis:a pilot study233Table I. Mean ± Standard Deviation (SD) Values at baseline and at the end of the study. BASDAI, Bath AnkylosingSpondylitis Disease Activity Index; BASFI, Bath Ankylosing Spondylitis Functional Index; VAS, visual analogue scale; CRP,C-reactive protein; ESR, erythrocyte sedimentation rate; NS, not significant.Baseline End pBASDAI Score 5.8 ± 1.5 4 ± 1.8 < 0.05 BASFI Score 33.6 ± 10 28.6 ± 6.3 NSVAS Score 58.1 ± 16.8 41.5 ± 14.3 < 0.05 CRP (mg/L) 25.2 ± 11 19.8 ± 6.4 NSESR (mm/hr) 28 ± 11.6 22.5 ± 7.1 NSM. Sanges, G. Valente, M. Rea, R. Della Gatta, G. De Franchis, R. Sollazzo, A. D’Arienzo These preliminary data suggest that the association of LA and LS determines a significantreduction in SpA activity and in patientʼs perception of pain. Moreover, these bacteria donʼt in-duce relapse of intestinal disease as non-steroidal anti-inflammatory drugs (NSAIDs) can do13.We believe that these probiotics may give a contribute in the management of SpA in patientswith UC. However, controlled randomized clinical trials are necessary to confirm these results.  References1) SCARPA R, DEL PUENTE A, D'ARIENZO A, DI GIROLAMO C, DELLA VALLE G, PANARESE A, LUBRANO E, ORIENTE P. Thearthritis of ulcerative colitis: clinical and genetic aspects. J Rheumatol 1992; 19: 373-377.2) WOLLHEIM FA. Enteropathic arthritis. In: Ruddy S, Harris ED Jr, Sledge CB, eds. Textbook of rheumatology, 6thed. Philadelphia: WB Saunders, 2001: pp 1081-1088.3) BERNSTEIN CN, BLANCHARD JF, RAWSTHORNE P, YU N. The prevalence of extraintestinal diseases in inflammato-ry bowel disease: A population-based study. Am J Gastroenterol 2001; 96: 1116-1122. 4) DOUGADOS M, VAN DER LINDEN S, JUHLIN R, HUITFELDT B, AMOR B, CALIN A, CATS A, DIJKMANS B, OLIVIERI I,PASERO G. The European Spondylarthropathy Study Group preliminary criteria for the classification of spondy-larthropathy. Arthritis Rheum 1991; 34: 1218-1227.5) TAUROG JD, RICHARDSON JA, CROFT JT, SIMMONS WA, ZHOU M, FERNANDEZ-SUEIRO JL, BALISH E, HAMMER RE.The germfree state prevents development of gut and joint inflammatory disease in HLA-B27 transgenic rats. JExp Med 1994; 180: 2359-2364.6) DAS KM. Relationship of extraintestinal involvements in inflammatory bowel disease: new insights into autoim-mune pathogenesis. Dig Dis Sci 1999; 44: 1-13.7) SHEIL B, MCCARTHY J, O'MAHONY L, BENNETT MW, RYAN P, FITZGIBBON JJ, KIELY B, COLLINS JK, SHANAHAN F. Isthe mucosal route of administration essential for probiotic function? Subcutaneous administration is associat-ed with attenuation of murine colitis and arthritis. Gut 2004; 53: 694-700.8) BAHARAV E, MOR F, HALPERN M, WEINBERGER A. Lactobacillus GG bacteria ameliorate arthritis in Lewis rats. JNutr 2004; 134: 1964-1969.9) SO JS, KWON HK, LEE CG, YI HJ, PARK JA, LIM SY, HWANG KC, JEON YH, IM SH. Lactobacillus casei suppress-es experimental arthritis by down-regulating T helper 1 effector functions. Mol Immunol 2008; 45: 2690-2699.10) SO JS, LEE CG, KWON HK, YI HJ, CHAE CS, PARK JA, HWANG KC, IM SH. Lactobacillus casei potentiates induc-tion of oral tolerance in experimental arthritis. Mol Immunol 2008; 46: 172-180.11) KARIMI O, PEÑA AS, VAN BODEGRAVEN AA. Probiotics (VSL#3) in arthralgia in patients with ulcerative colitis andCrohn's disease: a pilot study. Drugs Today (Barc) 2005; 41: 453-459.12) BROPHY S, BURROWS CL, BROOKS C, GRAVENOR MB, SIEBERT S, ALLEN SJ. Internet-based randomised controlledtrials for the evaluation of complementary and alternative medicines: probiotics in spondyloarthropathy. BMCMusculoskelet Disord 2008; 9: 4.13) TAKEUCHI K, SMALE S, PREMCHAND P, MAIDEN L, SHERWOOD R, THJODLEIFSSON B, BJORNSSON E, BJARNASON I.Prevalence and mechanism of nonsteroidal anti-inflammatory drug-induced clinical relapse in patients with in-flammatory bowel disease. Clin Gastroenterol Hepatol 2006; 4: 196-202.M. Sanges, G. Valente, M. Rea, R. Della Gatta, G. De Franchis, R. Sollazzo, A. D’Arienzo Gastroenterology Unit, Department of Clinicaland Experimental Medicine, AOU “Federico II”, Naples (Italy))Corresponding Author: Marco Sanges, MD, e-mail: marcosanges1974@libero.it234

Probiotics in spondyloarthropathy associated with ulcerative colitis: a pilot study

Probiotics in spondyloarthropathy associated with ulcerative colitis: a pilot study

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