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. 2021 Dec 13;2021:7552546. doi: 10.1155/2021/7552546

Table 3.

The characteristics of the included studies.

Study Country Sample size Intervention Relevant outcomes Inclusion criteria Exclusion criteria Mean age (years) Duration
Trial group Control group Trial group Control group Trial group Control group
Navarro-López et al. 2019 [15] Spanish 45 43 Oral probiotics (Bifidobacterium longum CECT 7347, B. lactis CECT 8145, and Lactobacillus rhamnosus CECT 8361) + topical corticosteroid betamethasone in combination with calcipotriol Oral placebo (maltodextrin) + topical corticosteroid betamethasone in combination with calcipotriol PASI75, adverse events Age between 18 and 70 years, diagnosis of plaque psoriasis at least one year prior to the study, mild or moderate severity (PASI > 6), and informed consent signed 1. Had exposure to systemic corticosteroids, methotrexate, cyclosporine, or biologic drugs in the previous 3 months
2. Antibiotics in the previous 2 weeks
3. Signs of bacterial infection
4. The diagnosis of liver disease with child-Pugh C index
5. Chronic renal insufficiency with creatinine clearance <50 ml/min or serum creatinine >1.5 mg/dl
6. Chronic endocrine, respiratory, neurological, or moderate to severe cardiovascular disease, as well as concomitant skin disease prior to the start of the study
41.57 ± 13.23 43.09 ± 10.32 12 weeks
Groeger et al. 2013 [16] Ireland 12 14 Oral probiotics (Bifidobacterium infantis 35264) Oral placebo (maltodextrin) CRP, TNF-α and IL-6 Aged between 18 and 60 y with mild to moderate chronic plaque psoriasis with a Psoriasis Area and Severity Index (PASI) < 16 1. Pregnant or breast feeding females
2. Individuals diagnosed with lactose intolerance or immunodeficiency
3. Individuals who had undergone any abdominal surgery (with the exception of hernia repair and appendectomy)
4. Individuals with a psychiatric illness or with significant hepatic, renal disease
8 weeks
Lu 2017 [17] China 25 25 Oral probiotics (combined Bifidobacterium, Lactobacillus, Enterococcus, and Bacillus) 1 g bid or tid + oral acitretin 10 mg tid; after 2 months, it was changed to 10 mg bid, and the dose was gradually reduced to 0 Oral acitretin 10 mg tid; after 2 months, it was changed to 10 mg bid, and the dose was gradually reduced to 0 Total effective rate, PASI75 1. The patient meets the diagnosis of psoriasis vulgaris in the “"Guiding Principles for Clinical Research of New Chinese Medicines”
2. Age from 18 to 70 years old
3. The patient or the patient's family voluntarily participate and sign the informed consent form
1. Received treatment for psoriasis within 1 month
2. Unusual psoriasis
3. Severe chronic diseases of the heart, liver, and kidneys or mental system diseases that make it impossible to communicate normally
4. Patients during pregnancy or lactation
51.3 ± 5.6 52.2 ± 5.9 12 weeks

PASI: psoriasis area and severity index; CRP: C-reaction protein; ESR: erythrocyte sedimentation rate.