ORAL VERSUS TRANSDERMAL ESTROGEN IN TURNER SYNDROME: A SYSTEMATIC REVIEW AND META-ANALYSIS

被引:15
|
作者
Zaiem, Feras [1 ]
Alahdab, Fares [1 ]
Al Nofal, Alaa [2 ]
Murad, Mohammad Hassan [1 ]
Javed, Asma [1 ]
机构
[1] Mayo Clin, Robert & Patricia E Kern Ctr Sci Hlth Care Delive, Rochester, MN 62335 USA
[2] Univ South Dakota, Dept Pediat, Sanford Children Specialty Clin, Pediat Endocrinol, Sioux Falls, SD USA
关键词
REPLACEMENT THERAPY; GROWTH-HORMONE; RANDOMIZED-TRIAL; GIRLS; WOMEN; BONE; 17-BETA-ESTRADIOL; OSTEOPOROSIS; SECRETION; DISEASE;
D O I
10.4158/EP161622.OR
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To conduct a systematic review and meta-analysis comparing transdermal estrogens (TDEs) versus oral estrogens (OEs) in Turner syndrome (TS). Methods: Randomized trials and observational comparative studies with a minimal follow-up of 6 months for skeletal and metabolic outcomes and serum hormone changes were included. Outcomes were pooled with a random effects model and are reported as mean differences between OE and TDE groups and 95% confidence intervals (CIs). Results: Of 845 candidate references, 4 studies were included. Both OEs and TDEs were associated with an increase in whole-body bone mineral density (BMD) z-score, with TDE therapy displaying a greater increase. OEs were associated with higher fasting glucose and total cholesterol. Both OEs and TDEs reduced low-density lipoprotein cholesterol (LDL-C) and increased high-density lipoprotein cholesterol (HDL-C), with OEs providing a more favorable effect. The use of 17-beta estradiol was associated with a higher total cholesterol and lower LDL-C than TDE. No statistically significant difference was found between OEs and TDEs in body mass index, fat mass, fat free mass, insulin-like growth factor 1, insulin-like growth factor binding protein 3, fasting insulin, triglycerides, estradiol, or estrone levels. Conclusion: In girls with TS, TDEs may be associated with a more beneficial effect on fasting glucose, cholesterol, and whole-body BMD. However, OEs have a more favorable impact on LDL-C and HDL-C. 17-beta estradiol has a more favorable effect on LDL-C.
引用
收藏
页码:408 / 421
页数:14
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