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1.
J Diabetes Complications ; 31(9): 1423-1429, 2017 Sep.
Article in English | MEDLINE | ID: mdl-28648555

ABSTRACT

AIMS: To evaluate and compare the association of four potential insulin resistance (IR) biomarkers (pigment-epithelium-derived factor [PEDF], retinol-binding-protein-4 [RBP-4], chitinase-3-like protein 1 [YKL-40] and brain-derived neurotrophic factor [BDNF]) with objective measures of IR. METHODS: We studied 81 subjects with different metabolic profiles. All participants underwent a 5-point OGTT with calculation of multiple IR indexes. A subgroup of 21 participants additionally underwent a hyperinsulinemic-euglycemic clamp. IR was defined as belonging to the highest quartile of incremental area under the insulin curve (iAUCins), or to the lowest quartile of the insulin sensitivity index (ISI). RESULTS: PEDF was associated with adiposity variables. PEDF and RBP4 increased linearly across quartiles of iAUCins (for PEDF p-trend=0.029; for RBP-4 p-trend=0.053). YKL-40 and BDNF were not associated with any adiposity or IR variable. PEDF and RBP-4 levels identified individuals with IR by the iAUCins definition: A PEDF cutoff of 11.9ng/mL had 60% sensitivity and 68% specificity, while a RBP-4 cutoff of 71.6ng/mL had 70% sensitivity and 57% specificity. In multiple regression analyses simultaneously including clinical variables and the studied biomarkers, only BMI, PEDF and RBP-4 remained significant predictors of IR. CONCLUSIONS: Plasma PEDF and RBP4 identified IR in subjects with no prior diagnosis of diabetes.


Subject(s)
Biomarkers/blood , Brain-Derived Neurotrophic Factor/blood , Chitinase-3-Like Protein 1/blood , Diagnostic Techniques, Endocrine , Eye Proteins/blood , Insulin Resistance , Nerve Growth Factors/blood , Retinol-Binding Proteins, Plasma/analysis , Serpins/blood , Adult , Aged , Female , Glucose Clamp Technique , Glucose Intolerance/blood , Glucose Intolerance/complications , Glucose Intolerance/diagnosis , Glucose Tolerance Test , Humans , Male , Middle Aged , Obesity/blood , Obesity/complications , Obesity/metabolism , Prediabetic State/blood , Prediabetic State/complications , Prediabetic State/diagnosis , Retinol-Binding Proteins, Plasma/metabolism
2.
J Clin Endocrinol Metab ; 85(9): 3365-9, 2000 Sep.
Article in English | MEDLINE | ID: mdl-10999835

ABSTRACT

Because the ovarian response to FSH stimulation in assisted reproduction is variable, ranging from hyporesponse to hyperresponse, with the possible complication of ovarian hyperstimulation, it would be of great benefit to predict the response of the patients to FSH. To date, no clear-cut predictors of ovarian responsiveness to FSH have been identified. In this study, we investigated the role of two distinct FSH receptor (FSHR) variants, Thr307/Asn680 and Ala307/Ser680, in the response to FSH in women undergoing controlled ovarian stimulation. The FSHR polymorphism at position 680 was analyzed by restriction-fragment-length polymorphism in 161 ovulatory women below the age of 40 yr. With reference to the couple, infertility has been diagnosed as being attributable to male causes (76%), tubal factor (11%), or both (13%). The distribution was 29% for the Asn/Asn, 45% for the Asn/Ser, and 26% for the Ser/Ser FSHR variant. Peak estradiol levels, number of preovulatory follicles, and number of retrieved oocytes were similar in the 3 groups. However, basal FSH levels were significantly different among the 3 groups (6.4 +/- 0.4 IU/L, 7.9 +/- 0.3 IU/L, and 8.3 +/- 0.6 IU/L for the Asn/Asn, Asn/Ser, and Ser/Ser groups, respectively, P < 0.01). The number of FSH ampoules required for successful stimulation was significantly different among the 3 groups (31.8 +/- 2.4, 40.7 +/- 2.3, and 46.8 +/- 5.0 for the Asn/Asn, Asn/Ser, and Ser/Ser groups, respectively, P < 0.05). According to multiple linear regression analysis, the number of ampoules needed could be predicted from a linear combination of both the type of polymorphism and basal FSH levels (P < 0.001). These clinical findings demonstrate that the ovarian response to FSH stimulation depends on the FSHR genotype.


Subject(s)
Follicle Stimulating Hormone/pharmacology , Ovary/drug effects , Receptors, FSH/drug effects , Receptors, FSH/genetics , Adult , DNA/genetics , DNA/isolation & purification , Female , Follicle Stimulating Hormone/blood , Genotype , Humans , Infertility, Female/genetics , Polymorphism, Genetic/genetics , Stimulation, Chemical
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