Lipidome and Microbiome Profile of Acne

• Status: Active, not recruiting
• Trial end date: 2027-01-01
• Target enrollment: 0
• Participant gender: All

Summary

Lipidome and microbiome analysis in subjects with acne on doxycycline. Investigators will look at the skin lipidome, blood lipidome, gut micro biome and skin micro biome.

Investigators will look at the changes between acne subjects and control participants, but also the changes that occur after the use of antibiotics and how this is altered.

• Phase: Phase 1/Phase 2
• Accepts Healthy Volunteers?: Accepts Healthy Volunteers

Details

• Lead Sponsor: University of California, Davis
• Treatments: Doxycycline

Criteria

Inclusion Criteria:

• Aged 15 and older

• Subjects/parents/legal guardian is able to read and comprehend study procedure and consent forms.

• Have already been prescribed Doxycycline by their physician for acne or to be eligible to be prescribed Doxycycline for acne

• Have acne that is diagnosed by a board certified dermatologist.

Exclusion Criteria:

• Those who have received systemic antibiotics within four weeks of starting the study.

• Those who have received systemic isotretinoin within six weeks of starting the study.

• Those with seborrheic dermatitis, rosacea, or polycystic ovary syndrome

• Those who are pregnant, prisoners or cognitively impaired.

• Those subjects who are currently using proton pump inhibits (as studies have shown this may impact the gut microbiome) (4)

• Those who have a BMI greater than >30 kg/m2, as studies have shown a reduction in the variability of intestinal microbes within this population (5).

• Those who have initiated or changed brand of oral contraceptive pill within 4 weeks of starting the study.

• Those who have autoimmune disorders as this group has been shown to have an altered microbiome (6)

• Those who have diabetes (6), immunodeficiencies (7), inflammatory bowel disease (6), hypercholesterolemia, as these groups have been shown to have altered gut microbiomes

• Those who have taken oral probiotic supplements (8) within 4 weeks of starting the study

• Given the nature of the instructions that need to be adhered to for accurate collection of samples and this data, non-English speaking individuals will be excluded from this pilot study.

• Allergies to the tetracycline group of antibiotics

• Those who do not fit the inclusion criteria