TY - JOUR
T1 - Effects of metformin on inappropriate LH release in women with polycystic ovarian syndrome and insulin resistance
AU - Ulloa-Aguirre, Alfredo
AU - Portocarrero, Lesly
AU - Zariñán, Teresa
AU - Olivares, Aleida
AU - Carranza-Lira, Sebastián
AU - Veldhuis, Johannes D.
AU - López-Alvarenga, Juan C.
N1 - Funding Information:
The authors are indebted to the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK; Bethesda, MD, USA) and Dr AF Parlow (Harbor-UCLA Medical Centre, Torrance, CA, USA) for the human FSH and LH RIA reagents and the anti-cAMP antibody. This study was supported by grant IMSS-2002/170 from the Fondo para el Fomento de la Investigación, Instituto Mexicano del Seguro Social, México. Leslie Portocarrero is a graduate student supported by the Consejo Nacional de Ciencia y Tecnología (CONACyT), México. Dr Alfredo Ulloa-Aguirre is recipient of a Research Career Development Award from the Fundación IMSS, México.
Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 2006/6
Y1 - 2006/6
N2 - The role of hyperinsulinaemia in neuroendocrine abnormalities in polycystic ovarian syndrome (PCOS) is controversial. The present study applied frequent blood sampling to assess the response of LH to metformin treatment in insulin-resistant women with PCOS. Thirteen predominantly overweight women with PCOS were studied before and after treatment with 1.5 g/day metformin for 3 months. Serum LH and testosterone were measured every 10 min for 10 h; LH was measured for an additional 2 h after gonadotrophin-releasing hormone (GnRH) administration. LH pulses were characterized by cluster analysis, secretory LH episodes by a deconvolution procedure, and synchronicity of paired LH-testosterone concentrations by lag-specific cross-correlation. After treatment, basal LH concentrations, amplitude of LH pulses, LH secretory amplitude, response to exogenous GnRH, and basal testosterone concentrations significantly decreased in seven patients, whereas in the remaining women these parameters remained unaltered. Before treatment, decreased coordinate LH and testosterone release was manifested by all patients; metformin treatment led to re-establishment of the feed-back control of testosterone on LH secretory rates by -20 to 0 min. Treatment did not modify the glucose:insulin ratio or serum insulin concentrations. In conclusion, administration of metformin allowed the identification of two subsets of PCOS women in whom neuroendocrine abnormalities may improve independently of the presence of insulin resistance or hyperinsulinaemia.
AB - The role of hyperinsulinaemia in neuroendocrine abnormalities in polycystic ovarian syndrome (PCOS) is controversial. The present study applied frequent blood sampling to assess the response of LH to metformin treatment in insulin-resistant women with PCOS. Thirteen predominantly overweight women with PCOS were studied before and after treatment with 1.5 g/day metformin for 3 months. Serum LH and testosterone were measured every 10 min for 10 h; LH was measured for an additional 2 h after gonadotrophin-releasing hormone (GnRH) administration. LH pulses were characterized by cluster analysis, secretory LH episodes by a deconvolution procedure, and synchronicity of paired LH-testosterone concentrations by lag-specific cross-correlation. After treatment, basal LH concentrations, amplitude of LH pulses, LH secretory amplitude, response to exogenous GnRH, and basal testosterone concentrations significantly decreased in seven patients, whereas in the remaining women these parameters remained unaltered. Before treatment, decreased coordinate LH and testosterone release was manifested by all patients; metformin treatment led to re-establishment of the feed-back control of testosterone on LH secretory rates by -20 to 0 min. Treatment did not modify the glucose:insulin ratio or serum insulin concentrations. In conclusion, administration of metformin allowed the identification of two subsets of PCOS women in whom neuroendocrine abnormalities may improve independently of the presence of insulin resistance or hyperinsulinaemia.
KW - Insulin resistance
KW - LH
KW - Metformin
KW - Polycystic ovarian syndrome
KW - Testosterone
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U2 - 10.1016/S1472-6483(10)61079-6
DO - 10.1016/S1472-6483(10)61079-6
M3 - Article
C2 - 16792841
AN - SCOPUS:33745049764
SN - 1472-6483
VL - 12
SP - 669
EP - 683
JO - Reproductive BioMedicine Online
JF - Reproductive BioMedicine Online
IS - 6
M1 - 2243
ER -