Inositol is a cyclohexane-hexol carbohydrate present in nine stereoisomeric forms,
best known as myo-inositol (MI) and D-chiro-inositol (DCI), with their
phosphorylated derivatives - inositol hexakisphosphate (InsP6) and the inositol
pyrophosphates. These molecules are membrane phospholipid components and
intracellular second messengers that participate in insulin signaling, calcium
regulation, DNA repair, and cellular energy transduction. Because of this function,
inositol supplementation has been investigated across a broad range of metabolic
and endocrine conditions. This review reveals current evidence on inositol's
biochemistry and its clinical influence on human metabolism. MI and DCI act as
insulin sensitizers by promoting GLUT4 translocation and glucose uptake; on the
other hand inositol pyrophosphates regulate adipocyte thermogenesis, lipid
handling, and insulin exocytosis in preclinical models. Meta-analysis pragmatically
shows that the use of MI supplements is effective in lowering BMI conservatively,
while it is very efficient in reducing the incidence of gestational diabetes mellitus
and fasting insulin levels in PCOS patients. The evidence in non-alcoholic fatty liver
disease is so far based on only one study in humans. By contrast, other reviews
showed only low-quality evidence that MI improves live birth or clinical pregnancy
rates in subfertile women with PCOS, and applications in thyroid disease,
psychiatric disorders, and cancer chemoprevention remain preliminary. MI is, for
the most part, well tolerated with mild gastrointestinal effects as the most common
adverse event. Inositol shows the strongest support for glycemic outcomes in
insulin-resistance. Its role in reproductive and other extra-metabolic applications
requires further high-quality trials.
Keywords: myo-inositol, inositol phosphates, PCOS, gestational diabetes mellitus,
human metabolism
