Are Young People with Turner Syndrome Who Have Undergone Treatment with Growth and Sex Hormones at Higher Risk of Metabolic Syndrome and Its Complications?

被引:2
|
作者
Krzyscin, Mariola [1 ]
Sowinska-Przepiera, Elzbieta [1 ,2 ]
Gruca-Stryjak, Karolina [3 ,4 ]
Soszka-Przepiera, Ewelina [5 ]
Syrenicz, Igor [2 ]
Przepiera, Adam [6 ]
Bumbuliene, Zana [7 ]
Syrenicz, Anhelli [2 ]
机构
[1] Pomeranian Med Univ, Dept Gynecol Endocrinol & Gynecol Oncol, Pediat & Adolescent Gynecol Clin, Unii Lubelskiej 1, PL-71252 Szczecin, Poland
[2] Pomeranian Med Univ, Dept Endocrinol Metab & Internal Dis, Unii Lubelskiej 1, PL-71252 Szczecin, Poland
[3] Poznan Univ Med Sci, Dept Perinatol & Gynecol, Poznan, Poland
[4] Ctr Med Genet GENESIS, Ul Dabrowskiego 77a, PL-60529 Poznan, Poland
[5] Pomeranian Med Univ, Dept Ophthalmol 2, Al Powstancow Wielkopolskich 72, PL-70111 Szczecin, Poland
[6] Pomeranian Med Univ, Dept Urol & Urol Oncol, Al Powstancow Wielkopolskich 72, PL-70111 Szczecin, Poland
[7] Vilnius Univ Hosp St aros Klin, Vilnius Univ Hosp Santaros Klin, Fac Med, Ctr Obstet & Gynecol, LT-03101 Vilnius, Lithuania
关键词
Turner syndrome; metabolic syndrome; body fat; visceral fat; recombinant human growth hormone; hormone replacement therapy; monosomy; mosaic karyotype; CARDIOMETABOLIC RISK; BLOOD-PRESSURE; CHILDREN; GIRLS; PREDICTORS; MASS;
D O I
10.3390/biomedicines12051034
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Introduction: Metabolic syndrome (MetS), characterized by visceral obesity, glucose abnormalities, hypertension and dyslipidemia, poses a significant risk of diabetes and cardiovascular disease. Turner syndrome (TS), resulting from X chromosome abnormalities, carries health complications. Despite growing evidence of an increased risk of MetS in women with TS, its prevalence and risk factors remain under investigation. These considerations are further complicated by the varying timing and dosages of treatment with growth hormone and sex hormones. Methods: We conducted a cross-sectional study comparing 44 individuals with TS with 52 age-matched control subjects. Growth hormone treatment in the study group was administered for varying lengths of time, depending on clinical response. We collected anthropometric, metabolic, endocrine and body composition data. Statistical analyses included logistic regression. Results: Baseline characteristics, including age, BMI and height, were comparable between the TS and control groups. Hormonally, individuals with TS showed lower levels of testosterone, DHEA-S, and cortisol, as well as elevated FSH. Lipid profiles indicated an atherogenic profile, and the body composition analysis showed increased visceral adipose tissue in those with TS. Other metabolic abnormalities were common in individuals with TS too, including hypertension and impaired fasting glucose levels. The risk of MetS components was assessed in subgroups according to karyotypes: monosomy 45X0 vs. other mosaic karyotypes. Logistic regression analysis showed a significant association between increased visceral adipose tissue in subjects with TS. Those with metabolic complications tended to have less muscle strength compared to those without these complications in both the study and control groups. Conclusions: This study highlights the unique metabolic and cardiovascular risk profile of individuals with TS, characterized by atherogenic lipids, higher levels of visceral adipose tissue and increased metabolic abnormalities. These findings underscore the importance of monitoring metabolic health in individuals with TS, regardless of age, BMI or karyotype, and suggest the potential benefits of lifestyle modification, building more muscle strength, and weight control strategies. Further research is needed to better understand and address the metabolic challenges faced by women with TS.
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页数:11
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