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Probiotic Intervention and Its Influence on Serum Leucine-Rich Alpha-2 Glycoprotein 1 Levels in Acne Vulgaris Patients

Probiotic Intervention and Its Influence on Serum Leucine-Rich Alpha-2 Glycoprotein 1 Levels in Acne Vulgaris Patients

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07277075
Enrollment
50
Registered
2025-12-11
Start date
2024-10-01
Completion date
2025-09-30
Last updated
2025-12-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acne Vulgaris, Influence, Probiotic, Serum Leucine-Rich Alpha-2 Glycoprotein 1

Brief summary

This study aimed to assess the serum level of Leucine-rich alpha-2 glycoprotein 1 (LRG1) in Acne vulgaris (AV) individuals and evaluate the effect of probiotic therapy on these serum levels.

Detailed description

Acne vulgaris (AV) is a common inflammatory disorder of the pilosebaceous units, characterized by the presence of inflammatory, non-inflammatory, or a combination of both types of lesions. Recent attention has turned toward biomarkers that reflect the inflammatory activity in acne and might act as indicators of disease severity, treatment response, or prognostic risk. One such candidate is Leucine-rich alpha-2 glycoprotein 1 (LRG1). Probiotics are live microorganisms that, when administered in sufficient quantities, can modulate the composition of the gut microbiota, helping reduce microbial dysbiosis, regulate the immune response, and decrease inflammatory mediators, thereby reducing systemic inflammatory burden, which is called the gut-skin-axis relationship.

Interventions

DIAGNOSTIC_TESTSerum Leucine-rich alpha-2 glycoprotein 1 (LRG1) level

Serum Leucine-rich alpha-2 glycoprotein 1 (LRG1) levels were assessed in acne vulgaris participants and healthy controls.

Sponsors

Benha University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age ≥18 years. * Both sexes. * Had not used systemic or topical acne therapy for at least two months or two weeks before the research, respectively. * Participants with clinically diagnosed mild to moderate acne vulgaris (AV) based on the Global Acne Grading System (GAGS)

Exclusion criteria

* Pregnancy. * Lactation. * History of hypersensitivity to probiotic components. * Smoking. * Presence of infections. * Autoimmune or malignant diseases. * Receiving any systemic therapy likely to affect the microbiome or inflammatory biomarkers.

Design outcomes

Primary

MeasureTime frameDescription
Serum Leucine-Rich Alpha-2 Glycoprotein 1 Level12 weeks after the therapySerum Leucine-Rich Alpha-2 Glycoprotein 1 Level was assessed.

Secondary

MeasureTime frameDescription
Acne severity12 weeks after the therapyAcne severity was assessed based on Global Acne Grading System (GASA) score is considered as 1-18 mild, 19-30 moderate, 31-38 severe, and \>39 very severe
Patient satisfaction12 weeks after the therapyPatient satisfaction was evaluated using the Likert scale, with response options ranging from 1 = very dissatisfied to 5 = very satisfied.

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026