Literature DB >> 17517238

Growth hormone treatment and left ventricular dimensions in Turner syndrome.

Lea Ann Matura1, Vandana Sachdev, Vladimir K Bakalov, Douglas R Rosing, Carolyn A Bondy.   

Abstract

OBJECTIVE: To determine whether cardiac dimensions were different in girls with Turner syndrome (TS) who received growth hormone (GH) compared with those who did not receive GH. STUDY
DESIGN: This retrospective, cross-sectional study analyzed echocardiograms in 86 females with TS divided into GH-treated (n = 67) and untreated (n = 19) groups. The subjects all participated in the National Institutes of Health protocol between 2001 and 2006.
RESULTS: The average age was 16.2 years (range, 10 to 25 years), and average duration of GH treatment was 4.4 years (range, 1 to 14 years). The GH-treated group was taller by approximately 7 cm (P = .004), but cardiac dimensions normalized to body surface area (BSA), including septal and posterior wall thickness and left ventricular (LV) mass and internal diameters, did not differ significantly between the 2 groups. The fractional shortening index was similar in the 2 groups. Multiple regression analyses indicated that BSA, but not duration of GH treatment, predicted LV dimensions in girls with TS.
CONCLUSIONS: GH treatment of girls with TS increases stature but does not disproportionately affect cardiac dimensions.

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Year:  2007        PMID: 17517238      PMCID: PMC1950786          DOI: 10.1016/j.jpeds.2007.02.009

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  25 in total

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2.  Final height in girls with turner syndrome after long-term growth hormone treatment in three dosages and low dose estrogens.

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6.  Medium-term cardiovascular effects of high-dose growth hormone treatment in growth hormone-deficient children.

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6.  The Usefulness of Magnetic Resonance Imaging of the Cardiovascular System in the Diagnostic Work-Up of Patients With Turner Syndrome.

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