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The Cutoff of Gonadotropins for Close Evaluation of Cardiometabolic Risk Factors in Turner Syndrome

BACKGROUND: Turner syndrome is a common genetic disorder in females. It is a disorder characterized by variable number of clinical features, so it needs a multidisciplinary approach for care. Therefore, we aimed to define the cutoff of gonadotropins for close evaluation of cardiometabolic risk facto...

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Autores principales: Koohmanaee, Shahin, Motamed, Behrang, Ghorbandoust, Sharareh, Badeli, Hamidreza, Rad, Afagh Hassanzadeh, Dalili, Setila, Darabipour, Zohre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9188885/
https://www.ncbi.nlm.nih.gov/pubmed/35706858
http://dx.doi.org/10.4103/ijpvm.IJPVM_321_20
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author Koohmanaee, Shahin
Motamed, Behrang
Ghorbandoust, Sharareh
Badeli, Hamidreza
Rad, Afagh Hassanzadeh
Dalili, Setila
Darabipour, Zohre
author_facet Koohmanaee, Shahin
Motamed, Behrang
Ghorbandoust, Sharareh
Badeli, Hamidreza
Rad, Afagh Hassanzadeh
Dalili, Setila
Darabipour, Zohre
author_sort Koohmanaee, Shahin
collection PubMed
description BACKGROUND: Turner syndrome is a common genetic disorder in females. It is a disorder characterized by variable number of clinical features, so it needs a multidisciplinary approach for care. Therefore, we aimed to define the cutoff of gonadotropins for close evaluation of cardiometabolic risk factors in Turner syndrome. METHODS: This is a case-control study on 31 patients with Turner syndrome and 31 healthy individuals. Clinical examination including blood pressure measurement and systems evaluation was performed. Laboratory testing, which included 12-h fasting, assessed lipid profile, glucose, and serum gonadotropin. RESULTS: Turner syndrome had a higher BMI, systolic, and diastolic blood pressure than the normal group (P < 0.001) Patients with Turner syndrome had significantly higher total cholesterol, low-density lipoprotein, triglyceride, and TG-to-high-density lipoprotein ratio compared to the healthy individuals (P < 0.05). With increasing LH and FSH, BMI values, systolic blood pressure, and total cholesterol increased significantly (P < 0.001). Serum TG levels in Turner syndrome were only positively correlated with LH and not correlated with FSH. The cutoff point of LH and FSH for triglyceride in upper 75 percentile were 31 (sensitivity = 38.1%, specificity = 80%) and 48 (sensitivity = 61.9%, specificity = 70%), respectively. CONCLUSIONS: Based on dyslipidemia and lower level of ejection fraction, considering cardiometabolic risk factors in lower age groups in Turner syndrome can be recommended.
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spelling pubmed-91888852022-06-14 The Cutoff of Gonadotropins for Close Evaluation of Cardiometabolic Risk Factors in Turner Syndrome Koohmanaee, Shahin Motamed, Behrang Ghorbandoust, Sharareh Badeli, Hamidreza Rad, Afagh Hassanzadeh Dalili, Setila Darabipour, Zohre Int J Prev Med Original Article BACKGROUND: Turner syndrome is a common genetic disorder in females. It is a disorder characterized by variable number of clinical features, so it needs a multidisciplinary approach for care. Therefore, we aimed to define the cutoff of gonadotropins for close evaluation of cardiometabolic risk factors in Turner syndrome. METHODS: This is a case-control study on 31 patients with Turner syndrome and 31 healthy individuals. Clinical examination including blood pressure measurement and systems evaluation was performed. Laboratory testing, which included 12-h fasting, assessed lipid profile, glucose, and serum gonadotropin. RESULTS: Turner syndrome had a higher BMI, systolic, and diastolic blood pressure than the normal group (P < 0.001) Patients with Turner syndrome had significantly higher total cholesterol, low-density lipoprotein, triglyceride, and TG-to-high-density lipoprotein ratio compared to the healthy individuals (P < 0.05). With increasing LH and FSH, BMI values, systolic blood pressure, and total cholesterol increased significantly (P < 0.001). Serum TG levels in Turner syndrome were only positively correlated with LH and not correlated with FSH. The cutoff point of LH and FSH for triglyceride in upper 75 percentile were 31 (sensitivity = 38.1%, specificity = 80%) and 48 (sensitivity = 61.9%, specificity = 70%), respectively. CONCLUSIONS: Based on dyslipidemia and lower level of ejection fraction, considering cardiometabolic risk factors in lower age groups in Turner syndrome can be recommended. Wolters Kluwer - Medknow 2022-04-08 /pmc/articles/PMC9188885/ /pubmed/35706858 http://dx.doi.org/10.4103/ijpvm.IJPVM_321_20 Text en Copyright: © 2022 International Journal of Preventive Medicine https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Koohmanaee, Shahin
Motamed, Behrang
Ghorbandoust, Sharareh
Badeli, Hamidreza
Rad, Afagh Hassanzadeh
Dalili, Setila
Darabipour, Zohre
The Cutoff of Gonadotropins for Close Evaluation of Cardiometabolic Risk Factors in Turner Syndrome
title The Cutoff of Gonadotropins for Close Evaluation of Cardiometabolic Risk Factors in Turner Syndrome
title_full The Cutoff of Gonadotropins for Close Evaluation of Cardiometabolic Risk Factors in Turner Syndrome
title_fullStr The Cutoff of Gonadotropins for Close Evaluation of Cardiometabolic Risk Factors in Turner Syndrome
title_full_unstemmed The Cutoff of Gonadotropins for Close Evaluation of Cardiometabolic Risk Factors in Turner Syndrome
title_short The Cutoff of Gonadotropins for Close Evaluation of Cardiometabolic Risk Factors in Turner Syndrome
title_sort cutoff of gonadotropins for close evaluation of cardiometabolic risk factors in turner syndrome
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9188885/
https://www.ncbi.nlm.nih.gov/pubmed/35706858
http://dx.doi.org/10.4103/ijpvm.IJPVM_321_20
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