Effect of Iron Depletion by Bloodletting vs. Observation on Oxidative Stress Biomarkers of Women with Functional Hyperandrogenism Taking a Combined Oral Contraceptive: A Randomized Clinical Trial.
Manuel Luque-RamírezAndrés E Ortiz-FloresMaría Ángeles Martínez-GarcíaMaría Rosa InsenserAlejandra Quintero-TobarSara De Lope QuiñonesElena Fernández-DuránMaría Lía Nattero-ChávezFrancisco Álvarez-BlascoHéctor Francisco Escobar-MorrealePublished in: Journal of clinical medicine (2022)
Women with functional hyperandrogenism show both increased markers of oxidative stress and a mild iron overload. Combined oral contraceptives (COC) may worsen redox status in the general population. Since iron depletion ameliorates oxidative stress in other iron overload states, we aimed to address the changes in the redox status of these women as a consequence of COC therapy and of bloodletting, conducting a randomized, controlled, parallel, open-label clinical trial in 33 adult women with polycystic ovary syndrome or idiopathic hyperandrogenism. After three months of treatment with a COC, participants were randomized (1:1) to three scheduled bloodlettings or observation for another nine months. After taking a COC, participants showed a mild decrease in their plasma electrochemical antioxidant capacity, considering fast-acting antioxidants [MD: -1.51 (-2.43 to -0.60) μC, p = 0.002], and slow-acting antioxidants [MD: -1.90 (-2.66 to -1.14) μC, p < 0.001]. Women submitted to bloodletting showed a decrease in their non-enzymatic antioxidant capacity levels (NEAC) throughout the trial, whereas those individuals in the control arm showed a mild increase in these levels at the end of the study (Wilks' λ: 0.802, F: 3.572, p = 0.041). Decreasing ferritin and plasma hemoglobin during the trial were associated with worse NEAC levels. COC may impair redox status in women with functional hyperandrogenism. Decreasing iron stores by scheduled bloodletting does not override this impairment.
Keyphrases
- polycystic ovary syndrome
- oxidative stress
- open label
- phase iii
- clinical trial
- phase ii
- iron deficiency
- insulin resistance
- study protocol
- double blind
- dna damage
- diabetic rats
- induced apoptosis
- gold nanoparticles
- pregnancy outcomes
- placebo controlled
- ischemia reperfusion injury
- molecular dynamics
- pregnant women
- squamous cell carcinoma
- adipose tissue
- randomized controlled trial
- nitric oxide
- metabolic syndrome
- radiation therapy
- mass spectrometry
- stem cells
- bone marrow
- skeletal muscle
- young adults
- mouse model
- molecularly imprinted
- heat shock
- combination therapy
- solid phase extraction