Myo-Inositol in Pregnancy: Implications for Acne Management

July 2026 | Volume 25 | Issue 7 | 611 | Copyright © July 2026


Published online June 29, 2026

Daniela Baboun BAa, Marita Yaghi MDb, Jennifer Keelin BSa, Daniella M. Hernandez-Bueso BSa, Valery Fernandez Fernandez BSc, Jonette Keri MDc

aHerbert Wertheim College of Medicine, Florida International University, Miami, FL
bDepartment of Dermatology, Larkin Health System, Miami, FL
cDepartment of Dermatology and Cutaneous Surgery, University of Miami Miller School of Medicine, Miami, FL

Abstract
Background: Acne vulgaris is common during pregnancy and presents unique therapeutic challenges due to fetal safety considerations and restrictions on conventional acne medications. Adjunctive strategies that target hormonal and metabolic contributors to acne without teratogenic risk are therefore of particular relevance to dermatologic care.
Objective: To review the evidence supporting myo-inositol as an adjunctive option for pregnancy-related acne and contextualize its dermatologic relevance within associated metabolic, endocrine, and psychosocial conditions.
Methods: A literature review of randomized controlled trials, systematic reviews, meta-analyses, observational studies, and mechanistic investigations evaluating myo-inositol in acne, polycystic ovary syndrome (PCOS), gestational diabetes mellitus (GDM), preeclampsia, fertility, mental health, sleep, and topical applications was conducted.
Results: Myo-inositol supplementation has been associated with reductions in acne severity, especially in patients with PCOS, along with improvements in insulin sensitivity and key metabolic parameters. In pregnancy, myo-inositol has been linked to reduced incidence of GDM, favorable endothelial and metabolic markers relevant to preeclampsia, and improved reproductive outcomes. Additional evidence suggests benefits for mood and sleep, factors that may indirectly influence acne. Available data support a favorable maternal and fetal safety profile, but evidence for topical myo-inositol in acne remains limited.
Conclusion: Myo-inositol may represent a safe adjunctive option for acne management during pregnancy, particularly in patients with metabolic or hyperandrogenic features. Although acne-specific pregnancy data are limited, existing mechanistic and safety evidence supports its consideration in dermatologic practice when therapeutic options are restricted.

INTRODUCTION

Acne vulgaris affects over 80% of young adults globally1 and up to 43% of pregnant women,2 with severity typically peaking in the third trimester.3 Pregnancy-related hormonal fluctuations, including elevations in androgens and progesterone, combined with increased sebaceous activity, contribute to acne exacerbation.4,5 While mild cases may resolve with limited intervention, moderate to severe acne can substantially impair quality of life. In one clinical sample, 7.1% of patients with acne reported suicidal ideation within the preceding 2 weeks.6 Management during pregnancy is further complicated by fetal safety concerns and contraindications to many conventional acne therapies, underscoring the need for safe adjunctive treatment options.

Topical agents such as azelaic acid, benzoyl peroxide, and keratolytics are commonly used, though therapeutic options remain limited by fetal safety concerns.1,7 Myo-inositol, a naturally occurring carbohydrate,8 has emerged as a potential adjunct with a favorable pregnancy safety profile. This review examines the dermatologic relevance of myo-inositol in pregnancy-related acne and contextualizes its use within associated conditions involving shared hormonal and metabolic pathways, including polycystic ovary syndrome (PCOS), gestational diabetes mellitus (GDM), preeclampsia, mental health, and sleep. Integration of acne-specific outcomes with robust pregnancy safety data informs dermatologic decision-making in a population with limited therapeutic options.

More than 15 years of clinical research support the safety of myo-inositol during pregnancy.9 Its use as an adjunct to folate supplementation has been evaluated in folate-resistant pregnancies9,10 and in women with prior neural tube defect-affected pregnancies,9,11 further supporting its maternal and fetal tolerability.