Evaluation of Serum Ceramides C16, C24, and Sphingosine-1-Phosphate (S1P) in Patients With Acne Vulgaris

ConditionAcne Vulgaris
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age15-40
SponsorSohag University

About this trial

Acne vulgaris is a common chronic inflammatory skin disorder that affects adolescents and young adults. Recent research has shown that lipid mediators, including ceramides and sphingolipids, play an important role in maintaining skin barrier function and inflammation.

This study aims to evaluate the serum levels of ceramide C16, ceramide C24, and sphingosine-1-phosphate (S1P) in patients with acne vulgaris and compare them to healthy controls. The goal is to explore their possible role in the pathogenesis and severity of acne. Blood samples will be collected from participants, and quantitative analysis will be performed using liquid chromatography-tandem mass spectrometry (LC-MS/MS).

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

For Case Group

Both males and females aged 15-40 years.

Mild, Moderate, severe and very severe cases will be included. 5

Disqualifiers

Presence of any dermatological condition other than acne vulgaris (for cases).

Use of systemic or topical treatment such as isotretinoin or antibiotics within the last 3 months.

Pregnancy or lactation.

History of lipid-lowering therapy or supplements affecting ceramide or sphingolipid metabolism.

Trial population

Study Population: A. Inclusion Criteria: For Case Group This group will consist of (40) patients : * Both males and females aged 15-40 years. * Mild, Moderate, severe and very severe cases will be included. 5 For Control Group: • This group will consist of age- and sex-matched (40) healthy volunteers. B. Exclusion Criteria (for both groups): * Presence of any dermatological condition other than acne vulgaris (for cases). * Use of systemic or topical treatment such as isotretinoin or antibiotics within the last 3 months. * Pregnancy or lactation. * History of lipid-lowering therapy or supplements affecting ceramide or sphingolipid metabolism

Trial design

Design model

Case-control

Time perspective

Cross-sectional

Treatments tested in this trial

  • Blood sample collection for biochemical analysis of serum ceramides (C16, C24) and sphingosine-1-phosphate (S1P).

    Other intervention

    Venous blood samples (5 mL) will be collected from all participants under aseptic conditions. Serum will be separated and stored at -80°C until analysis. Quantitative estimation of ceramide C16, ceramide C24, and sphingosine-1-phosphate (S1P) will be performed using liquid chromatography-tandem mass spectrometry (LC-MS/MS). No therapeutic intervention will be given.

Treatment groups

80 Participants
are divided into 2 treatment groups
Group A: Acne vulgaris patients1 intervention
Group B: Healthy controls1 intervention

Trial outcomes

Primary outcomes

1

Serum levels of Ceramide C16, Ceramide C24, and Sphingosine-1-Phosphate (S1P)

Quantitative assessment of serum concentrations of Ceramide C16, Ceramide C24, and Sphingosine-1-Phosphate (S1P) in acne vulgaris patients and healthy controls using liquid chromatography-tandem mass spectrometry (LC-MS/MS).

Time frame
At baseline (single visit)

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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