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Erschienen in: Endocrine 3/2011

01.12.2011 | Original Article

Growth hormone effect on body composition in Turner syndrome

verfasst von: Alexandre Duarte Baldin, Tatiana Fabbri, Adriana Aparecida Siviero-Miachon, Angela Maria Spinola-Castro, Sofia Helena Valente de Lemos-Marini, Maria Tereza Matias Baptista, Lilia Freire Rodrigues D’Souza-Li, Andrea Trevas Maciel-Guerra, Gil Guerra-Junior

Erschienen in: Endocrine | Ausgabe 3/2011

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Abstract

This study analyzes the body composition of young adult women with Turner syndrome (TS) either treated or not treated with recombinant human growth hormone (rhGH) and compares them with a group of healthy women. Fifty-two non-treated TS patients (23.0 ± 5.8 years), 30 treated with rhGH (21.5 ± 1.5 years), and 133 healthy young adult women (22.9 ± 3.2 years) were evaluated regarding height (H) and weight, body mass index (BMI), brachial perimeter and tricipital cutaneous fold (fat and lean areas at the arm), sitting height (SRH = sitting height/H × 100), leg length (leg/H), waist and hip circumferences (waist/hip), and bioimpedance (percentages of water, lean mass, and fat mass). Age at start of rhGH therapy varied from 7.8 to 15.1 years (10.0 ± 1.3 years), duration of treatment from 2.8 to 8.2 years (3.7 ± 1.5 years), and the mean dose was 0.42 mg/kg/w (from 0.32 to 0.50 mg/kg/w). Body composition (except height) did not differ between TS groups, but there were differences when compared to the control group: weight and sitting height were lower in TS patients; and BMI, SHR, and leg/H were higher. There was an association between all groups with regards to BMI, waist, SHR, and leg/H, but not in percentage of fat mass. SHR was positively correlated with BMI, waist, hip, and percentage of fat mass. This sample of TS patients (with and without rhGH therapy) did not differ in BMI or body composition. However, there were differences between patients with TS patients and normal healthy women. Regardless of rhGH therapy, TS patients should be monitored, particularly for sitting height, SHR, leg length, leg/H, and waist/hip.
Literatur
3.
Zurück zum Zitat M.L. Davenport, N. Punyasavatsut, D. Gunther, L. Savendahl, P.W. Stewart, Turner syndrome: a pattern of early growth failure. Acta Paediatr. Suppl. 88, 118–121 (1999)PubMedCrossRef M.L. Davenport, N. Punyasavatsut, D. Gunther, L. Savendahl, P.W. Stewart, Turner syndrome: a pattern of early growth failure. Acta Paediatr. Suppl. 88, 118–121 (1999)PubMedCrossRef
4.
Zurück zum Zitat S.H. De Lemos-Marini, A.M. Morcillo, M.T. Baptista, G. Guerra-Jr, A.T. Maciel-Guerra, Spontaneous final height in Tuner′s syndrome in Brazil. J. Pediatr. Endocrionol. Metab. 20, 1207–1214 (2009)CrossRef S.H. De Lemos-Marini, A.M. Morcillo, M.T. Baptista, G. Guerra-Jr, A.T. Maciel-Guerra, Spontaneous final height in Tuner′s syndrome in Brazil. J. Pediatr. Endocrionol. Metab. 20, 1207–1214 (2009)CrossRef
5.
Zurück zum Zitat C.A. Bondy, Turner Syndrome Study Group, Care of girls and women with Turner syndrome: a guideline of the Turner Syndrome Study Group. J. Clin. Endocrinol. Metab. 92, 10–25 (2007)PubMedCrossRef C.A. Bondy, Turner Syndrome Study Group, Care of girls and women with Turner syndrome: a guideline of the Turner Syndrome Study Group. J. Clin. Endocrinol. Metab. 92, 10–25 (2007)PubMedCrossRef
6.
Zurück zum Zitat V.K. Bakalov, M.M. Cooley, M.J. Quon, M.L. Luo, J.A. Yanovski, L.M. Nelson, Impaired insulin secretion in the Turner metabolic syndrome. J. Clin. Endocrinol. Metab. 89, 3516–3520 (2004)PubMedCrossRef V.K. Bakalov, M.M. Cooley, M.J. Quon, M.L. Luo, J.A. Yanovski, L.M. Nelson, Impaired insulin secretion in the Turner metabolic syndrome. J. Clin. Endocrinol. Metab. 89, 3516–3520 (2004)PubMedCrossRef
7.
Zurück zum Zitat T. Morgan, Turner syndrome: diagnosis and management. Am. Fam. Physician 76, 405–410 (2007)PubMed T. Morgan, Turner syndrome: diagnosis and management. Am. Fam. Physician 76, 405–410 (2007)PubMed
8.
Zurück zum Zitat C. Lichiardopol, M. Mota, D. Braicu, C. Militaru, F. Mixich, Diabetes mellitus and Turner syndrome. Rom. J. Intern. Med. 45, 299–304 (2007)PubMed C. Lichiardopol, M. Mota, D. Braicu, C. Militaru, F. Mixich, Diabetes mellitus and Turner syndrome. Rom. J. Intern. Med. 45, 299–304 (2007)PubMed
9.
Zurück zum Zitat C.H. Gravholt, B.E. Hjerrild, L. Mosekilde, T.K. Hansen, L.M. Rasmussen, J. Frystyk, Body composition is distinctly altered in Turner syndrome: relations to glucose metabolism, circulating adipokines, and endothelial adhesion molecules. Eur. J. Endocrinol. 155, 583–592 (2006)PubMedCrossRef C.H. Gravholt, B.E. Hjerrild, L. Mosekilde, T.K. Hansen, L.M. Rasmussen, J. Frystyk, Body composition is distinctly altered in Turner syndrome: relations to glucose metabolism, circulating adipokines, and endothelial adhesion molecules. Eur. J. Endocrinol. 155, 583–592 (2006)PubMedCrossRef
10.
Zurück zum Zitat J. Lo, Does growth hormone therapy benefit body composition and glucose homeostasis in girls with Turner syndrome? Nat. Clin. Pract. Endocrinol. Metab. 4, 596–597 (2008)PubMedCrossRef J. Lo, Does growth hormone therapy benefit body composition and glucose homeostasis in girls with Turner syndrome? Nat. Clin. Pract. Endocrinol. Metab. 4, 596–597 (2008)PubMedCrossRef
11.
Zurück zum Zitat M. Elsheikh, G.S. Conway, The impact of obesity on cardiovascular risk factors in Turner’s syndrome. Clin. Endocrinol. 49, 447–450 (1998)CrossRef M. Elsheikh, G.S. Conway, The impact of obesity on cardiovascular risk factors in Turner’s syndrome. Clin. Endocrinol. 49, 447–450 (1998)CrossRef
12.
Zurück zum Zitat P.R. Blackett, A.C. Rundle, J. Frane, S.L. Blethen, Body mass index (BMI) in Turner syndrome before and during growth hormone (GH) therapy. Int. J. Obes. Relat. Metab. Disord. 24, 232–235 (2000)PubMedCrossRef P.R. Blackett, A.C. Rundle, J. Frane, S.L. Blethen, Body mass index (BMI) in Turner syndrome before and during growth hormone (GH) therapy. Int. J. Obes. Relat. Metab. Disord. 24, 232–235 (2000)PubMedCrossRef
13.
Zurück zum Zitat N. Wooten, V.K. Bakalov, S. Hill, C.A. Bondy, Reduced abdominal adiposity and improved glucose tolerance in growth hormone-treated girls with Turner syndrome. J. Clin. Endocrinol. Metab. 93, 2109–2114 (2008)PubMedCrossRef N. Wooten, V.K. Bakalov, S. Hill, C.A. Bondy, Reduced abdominal adiposity and improved glucose tolerance in growth hormone-treated girls with Turner syndrome. J. Clin. Endocrinol. Metab. 93, 2109–2114 (2008)PubMedCrossRef
14.
Zurück zum Zitat M. Ari, V.K. Bakalov, S. Hill, C.A. Bondy, The effects of growth hormone treatment on bone mineral density and body composition in girls with Turner syndrome. J. Clin. Endocrinol. Metab. 91, 4302–4359 (2006)PubMedCrossRef M. Ari, V.K. Bakalov, S. Hill, C.A. Bondy, The effects of growth hormone treatment on bone mineral density and body composition in girls with Turner syndrome. J. Clin. Endocrinol. Metab. 91, 4302–4359 (2006)PubMedCrossRef
15.
Zurück zum Zitat J.A. Delgado, C.M. Trahms, V.P. Sybert, Measurement of body fat in Turner syndrome. Clin. Genet. 29, 291–297 (1986)PubMedCrossRef J.A. Delgado, C.M. Trahms, V.P. Sybert, Measurement of body fat in Turner syndrome. Clin. Genet. 29, 291–297 (1986)PubMedCrossRef
16.
Zurück zum Zitat T. Isojima, S. Yokoya, J. Ito, R. Horikawa, T. Tanaka, Inconsistent determination of overweight by two anthropometric indices in girls with Turner syndrome. Acta Paediatr. 98, 513–518 (2009)PubMedCrossRef T. Isojima, S. Yokoya, J. Ito, R. Horikawa, T. Tanaka, Inconsistent determination of overweight by two anthropometric indices in girls with Turner syndrome. Acta Paediatr. 98, 513–518 (2009)PubMedCrossRef
17.
Zurück zum Zitat A.R. Frisancho, New norms of upper limb fat and muscle areas for assessment of nutritional status. Am. J. Clin. Nutr. 34, 2540–2545 (1981)PubMed A.R. Frisancho, New norms of upper limb fat and muscle areas for assessment of nutritional status. Am. J. Clin. Nutr. 34, 2540–2545 (1981)PubMed
18.
Zurück zum Zitat R.F. Kuschner, Bioelectrical impedance analysis: a review of principles and applications. J. Am. Coll. Nutr. 11, 199–209 (1992) R.F. Kuschner, Bioelectrical impedance analysis: a review of principles and applications. J. Am. Coll. Nutr. 11, 199–209 (1992)
19.
Zurück zum Zitat E.C. Corrigan, L.M. Nelson, V.K. Bakalov, J.A. Yanovski, V.H. Vanderhoof, L.B. Yanoff, C.A. Bondy, Effects of ovarian failure and X-chromosome deletion on body composition and insulin sensitivity in young women. Menopause 13, 911–916 (2006)PubMedCrossRef E.C. Corrigan, L.M. Nelson, V.K. Bakalov, J.A. Yanovski, V.H. Vanderhoof, L.B. Yanoff, C.A. Bondy, Effects of ovarian failure and X-chromosome deletion on body composition and insulin sensitivity in young women. Menopause 13, 911–916 (2006)PubMedCrossRef
20.
Zurück zum Zitat F. Darendeliler, Z. Aycan, E. Cetinkaya, S. Vidilisan, F. Bas, A. Bideci, F. Demirel, Effects of growth hormone on growth, insulin resistance and related hormones (ghrelin, leptin and adiponectin) in Turner syndrome. Horm. Res. 68, 1–7 (2007)PubMedCrossRef F. Darendeliler, Z. Aycan, E. Cetinkaya, S. Vidilisan, F. Bas, A. Bideci, F. Demirel, Effects of growth hormone on growth, insulin resistance and related hormones (ghrelin, leptin and adiponectin) in Turner syndrome. Horm. Res. 68, 1–7 (2007)PubMedCrossRef
21.
Zurück zum Zitat C.H. Gravholt, R.W. Naeraa, Reference values for body proportions and body composition in adult women with Ulrich-Turner syndrome. Am. J. Med. Genet. 72, 403–408 (1997)PubMedCrossRef C.H. Gravholt, R.W. Naeraa, Reference values for body proportions and body composition in adult women with Ulrich-Turner syndrome. Am. J. Med. Genet. 72, 403–408 (1997)PubMedCrossRef
22.
Zurück zum Zitat A.D. Baldin, T. Fabbri, A.A. Siviero-Miachon, A.M. Spinola-Castro, S.H.V. Lemos-Marini, M.T.M. Baptista, L.F.R. D’Souza-Li, A.T. Maciel-Guerra, G. Guerra-Junior, Effects of growth hormone on body proportions in Turner syndrome compared with non-treated patients and normal women. J. Endocrinol. Invest. 33, 691–695 (2010)PubMed A.D. Baldin, T. Fabbri, A.A. Siviero-Miachon, A.M. Spinola-Castro, S.H.V. Lemos-Marini, M.T.M. Baptista, L.F.R. D’Souza-Li, A.T. Maciel-Guerra, G. Guerra-Junior, Effects of growth hormone on body proportions in Turner syndrome compared with non-treated patients and normal women. J. Endocrinol. Invest. 33, 691–695 (2010)PubMed
23.
Zurück zum Zitat A.M. Ottesen, L. Aksglaede, J. Garn, N. Tartaglia, F. Tassane, C.H. Gravholt, A. Bojesen, K. Sorensen, J. Niels, E. Rajpert-de-Meyts, T. Gerdes, A.-M. Lind, S. Kjaergaard, A. Juul, Increased number of sex chromosomes affects height in nonlinear fashion: a study of 305 patients with sex chromosome aneuploidy. Am. J. Med. Genet. A 152A, 1206–1212 (2010)PubMedCrossRef A.M. Ottesen, L. Aksglaede, J. Garn, N. Tartaglia, F. Tassane, C.H. Gravholt, A. Bojesen, K. Sorensen, J. Niels, E. Rajpert-de-Meyts, T. Gerdes, A.-M. Lind, S. Kjaergaard, A. Juul, Increased number of sex chromosomes affects height in nonlinear fashion: a study of 305 patients with sex chromosome aneuploidy. Am. J. Med. Genet. A 152A, 1206–1212 (2010)PubMedCrossRef
24.
Zurück zum Zitat G. Binder, Short stature due to SHOX deficiency: genotype, phenotype, and therapy. Horm. Res. Paediatr. 75, 81–89 (2011)PubMedCrossRef G. Binder, Short stature due to SHOX deficiency: genotype, phenotype, and therapy. Horm. Res. Paediatr. 75, 81–89 (2011)PubMedCrossRef
25.
Zurück zum Zitat E.N.N. Bannink, R.L.F. van der Palsen, P.G.H. Mulden, Long-term follow-up of GH-treated girls with Turner syndrome: BMI, blood pressure, body proportions. Horm. Res. 71, 336–342 (2009)PubMedCrossRef E.N.N. Bannink, R.L.F. van der Palsen, P.G.H. Mulden, Long-term follow-up of GH-treated girls with Turner syndrome: BMI, blood pressure, body proportions. Horm. Res. 71, 336–342 (2009)PubMedCrossRef
26.
Zurück zum Zitat L.A. Menke, T.C.I. Sas, G.R.I. Zandwjjken, M.A.I. de Ridder, T. Stjinen, S.M.P.F. de Munick Keizer-Schrama, B.J. Otten, J.M. Wit, The effect of oxandrolone on body proportions and body composition in growth hormone treated girls with Turner syndrome. Clin. Endocrinol. 73, 212–219 (2010) L.A. Menke, T.C.I. Sas, G.R.I. Zandwjjken, M.A.I. de Ridder, T. Stjinen, S.M.P.F. de Munick Keizer-Schrama, B.J. Otten, J.M. Wit, The effect of oxandrolone on body proportions and body composition in growth hormone treated girls with Turner syndrome. Clin. Endocrinol. 73, 212–219 (2010)
27.
Zurück zum Zitat L. Hagenäs, T. Hertel, Skeletal dysplasia, growth hormone treatment, body proportion: comparison with other syndromic and non-syndromic short children. Horm. Res. 60(suppl 3), 65–70 (2003)PubMed L. Hagenäs, T. Hertel, Skeletal dysplasia, growth hormone treatment, body proportion: comparison with other syndromic and non-syndromic short children. Horm. Res. 60(suppl 3), 65–70 (2003)PubMed
28.
Zurück zum Zitat B. Bogin, M.I. Varela-Silva, Leg length, body proportion, and health: a review with note on beauty. Int. J. Environ. Res. Public Health 7, 1047–1075 (2010)PubMedCrossRef B. Bogin, M.I. Varela-Silva, Leg length, body proportion, and health: a review with note on beauty. Int. J. Environ. Res. Public Health 7, 1047–1075 (2010)PubMedCrossRef
Metadaten
Titel
Growth hormone effect on body composition in Turner syndrome
verfasst von
Alexandre Duarte Baldin
Tatiana Fabbri
Adriana Aparecida Siviero-Miachon
Angela Maria Spinola-Castro
Sofia Helena Valente de Lemos-Marini
Maria Tereza Matias Baptista
Lilia Freire Rodrigues D’Souza-Li
Andrea Trevas Maciel-Guerra
Gil Guerra-Junior
Publikationsdatum
01.12.2011
Verlag
Springer US
Erschienen in
Endocrine / Ausgabe 3/2011
Print ISSN: 1355-008X
Elektronische ISSN: 1559-0100
DOI
https://doi.org/10.1007/s12020-011-9504-z

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