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Micronutrients in support to the one carbon cycle for the modulation of blood fasting homocysteine in PCOS women

Authors :
Schiuma, N.
Costantino, A.
Bartolotti, T.
Dattilo, M.
Bini, V.
Aglietti, M. C.
Renga, M.
Favilli, A.
Falorni, A.
Gerli, S.
Source :
Journal of Endocrinological Investigation; 20240101, Issue: Preprints p1-8, 8p
Publication Year :
2024

Abstract

Purpose: Fasting blood homocysteine is increased in PCOS women and is involved in several of its co-morbidities including cardiovascular disease and infertility. Corrective interventions based on the administration of supra-physiologic doses of folic acid work to a low extent. We aimed to test an alternative approach. Methods: This was a prospective, randomized, parallel group, open label, controlled versus no treatment clinical study. PCOS women aged > 18, free from systemic diseases and from pharmacological treatments were randomized with a 2:1 ratio for treatment with activated micronutrients in support to the carbon cycle (Impryl, Parthenogen, Switzerland—n= 22) or no treatment (n= 10) and followed-up for 3 months. Fasting blood homocysteine, AMH, testosterone, SHBGs, and the resulting FTI were tested before and at the end of the follow-up. Results: The mean baseline fasting blood homocysteine was above the normal limit of 12 μMol/L and inversely correlated with SHBG. AMH was also increased, whereas testosterone, SHBG, and FTI were within the normal limit. The treatment achieved a significant reduction of homocysteine, that did not change in the control group, independently of the starting value. The treatment also caused an increase of AMH and a decrease of SHBGs only in the subgroup with a normal homocysteine at baseline. Conclusions: In PCOS ladies, blood homocysteine is increased and inversely correlated with the SHBGs. Physiologic amounts of activated micronutrients in support to the carbon cycle achieve a reduction virtually in all exposed patients. Whether this is of clinical benefit remains to be established.

Details

Language :
English
ISSN :
03914097 and 17208386
Issue :
Preprints
Database :
Supplemental Index
Journal :
Journal of Endocrinological Investigation
Publication Type :
Periodical
Accession number :
ejs52257953
Full Text :
https://doi.org/10.1007/s40618-019-01163-x