Health-related quality of life in short children born small for gestational age: effects of growth hormone treatment and postponement of puberty.

Abstract:

AIMS:To investigate health-related quality of life (HRQoL) in short children born small for gestational age (SGA) during growth hormone (GH) treatment and additional postponement of puberty by gonadotropin-releasing hormone analogue (GnRHa). METHODS:HRQoL was studied longitudinally during 2 years of treatment in 97 short SGA children (mean age 11.6 years at start). The children were divided into three groups: prepubertal GH-treated (prep-GH) children, pubertal GH-treated (pub-GH) children, and pubertal GH-treated children with additional GnRHa treatment (pub-GH/GnRHa). HRQoL was measured by generic (TACQOL) and short stature-specific (TACQOL-S) questionnaires. RESULTS:The TACQOL-S showed that prep-GH children experienced significant HRQoL improvement on the subscales 'contact with adults', 'body image' and 'vitality', and pub-GH/GnRHa children on the subscales 'contact with adults', 'contact with peers' and 'physical abilities'. Parents of prep-GH and pub-GH/GnRHa children reported significant HRQoL improvement on most TACQOL-S scales, whereas HRQoL improvement in pub-GH children reached significance for 'future prospects' only. The HRQoL gain was similar in the three groups, also after correction for confounders. The generic questionnaire TACQOL did not reveal any changes. CONCLUSIONS:HRQoL improved in prepubertal and pubertal short SGA children during GH treatment. Additional GnRHa treatment had no adverse effect on the HRQoL gain. Disorder-specific questionnaires were particularly appropriate to evaluate HRQoL in children treated for short stature.

journal_name

Horm Res Paediatr

authors

Lem AJ,Jobse I,van der Kaay DC,de Ridder MA,Raat H,Hokken-Koelega AC

doi

10.1159/000337218

subject

Has Abstract

pub_date

2012-01-01 00:00:00

pages

170-9

issue

3

eissn

1663-2818

issn

1663-2826

pii

000337218

journal_volume

77

pub_type

杂志文章
  • Metabolic benefits of growth hormone therapy in idiopathic short stature.

    abstract::The US Food and Drug Administration approved use of recombinant human growth hormone (GH) for the treatment of idiopathic short stature (ISS) in children; however, few studies have evaluated metabolic outcomes. This article addresses whether children with ISS treated with GH experience the same metabolic benefits as c...

    journal_title:Hormone research in paediatrics

    pub_type: 杂志文章,评审

    doi:10.1159/000330165

    authors: Dahlgren J

    更新日期:2011-01-01 00:00:00

  • A Novel GNAS Mutation Causing Isolated Infantile Cushing's Syndrome.

    abstract::Infantile Cushing's syndrome is potentially found as part of McCune-Albright syndrome (MAS) which is caused by postzygotic somatic mutations of the GNAS gene. MAS is typically characterized by a triad of polyostotic fibrous dysplasia, café-au-lait skin pigmentation, and precocious puberty or other endocrine hyperfunct...

    journal_title:Hormone research in paediatrics

    pub_type:

    doi:10.1159/000501169

    authors: Dejkhamron P,Ittiwut C,TangNgam H,Sunkonkit K,Natesirinilkul R,Suphapeetiporn K,Shotelersuk V

    更新日期:2019-01-01 00:00:00

  • Exploring clinician confidence in the management of adolescent menstrual and reproductive health problems.

    abstract:PURPOSE:A high incidence of menstrual problems is reported in adolescent girls, with significant attendant morbidity. The majority are likely to be seen and managed by doctors other than specialist gynaecologists. This study aimed to survey the practice of doctors other than gynaecologists, to establish their chosen th...

    journal_title:Hormone research in paediatrics

    pub_type: 临床试验,杂志文章

    doi:10.1159/000356920

    authors: Neylon OM,Grover SR,Zacharin M

    更新日期:2014-01-01 00:00:00

  • Continuous Intragastric Dextrose: A Therapeutic Option for Refractory Hypoglycemia in Congenital Hyperinsulinism.

    abstract::Feeding problems are frequent in infants with congenital hyperinsulinism (HI) and may be exacerbated by continuous enteral nutrition (EN) used to maintain euglycemia. Our center's HI team uses dextrose solution given continuously via gastric tube (intrasgastric dextrose, IGD) for infants not fully responsive to conven...

    journal_title:Hormone research in paediatrics

    pub_type: 临床试验

    doi:10.1159/000491105

    authors: Vajravelu ME,Congdon M,Mitteer L,Koh J,Givler S,Shults J,De León DD

    更新日期:2019-01-01 00:00:00

  • Molecular and trophic mechanisms of pituitary tumourigenesis.

    abstract:BACKGROUND:The paradox of pituitary tumours is that persistent growth is so atypical. By definition, all pituitary microadenomas regain complete trophic stability after an initial period of deregulated growth. Unlike tumours in many other organ systems, concern about significant growth of macroadenoma remnants after de...

    journal_title:Hormone research in paediatrics

    pub_type:

    doi:10.1159/000329114

    authors: Levy A

    更新日期:2011-01-01 00:00:00

  • Thyroid function patterns at Hashimoto's thyroiditis presentation in childhood and adolescence are mainly conditioned by patients' age.

    abstract:BACKGROUND:There are few studies investigating the factors which may affect different biochemical presentations of Hashimoto's thyroiditis (HT) and these are frequently based on limited pediatric populations. AIMS:(1) To assess the frequency of thyroid function patterns at HT diagnosis in 608 children and adolescents,...

    journal_title:Hormone research in paediatrics

    pub_type: 杂志文章,多中心研究

    doi:10.1159/000343815

    authors: Wasniewska M,Corrias A,Salerno M,Mussa A,Capalbo D,Messina MF,Aversa T,Bombaci S,De Luca F,Valenzise M

    更新日期:2012-01-01 00:00:00

  • Congenital Hypothyroidism: 8-Year Experience Using 2 Newborn Screens in Alabama.

    abstract:BACKGROUND/AIMS:Newborn screening protocols for congenital hypothyroidism (CH) vary as to whether a TSH or T4 algorithm or some combination is performed. We aimed to determine the 3-year clinical outcome of infants diagnosed with CH and screen-positive for CH using a 2-screen protocol that measures both T4 and TSH on a...

    journal_title:Hormone research in paediatrics

    pub_type: 临床试验,杂志文章

    doi:10.1159/000501395

    authors: Pitts L,McCormick W,Mick GJ

    更新日期:2019-01-01 00:00:00

  • Second Trimester Maternal Leptin Levels Are Associated with Body Mass Index and Gestational Weight Gain but not Birth Weight of the Infant.

    abstract:INTRODUCTION:Obesity is increasing among the pregnant population. Leptin has an important role in the regulation of energy balance and hunger. The aim of this study was to investigate the association between maternal leptin levels with maternal obesity, gestational weight gain (GWG), single nucleotide polymorphisms (SN...

    journal_title:Hormone research in paediatrics

    pub_type: 临床试验,杂志文章

    doi:10.1159/000503422

    authors: Serapio S,Ahlsson F,Larsson A,Kunovac Kallak T

    更新日期:2019-01-01 00:00:00

  • Adult height and epigenotype in children with Silver-Russell syndrome treated with GH.

    abstract:AIMS:To compare adult heights of GH-treated and GH-untreated patients with Silver-Russell syndrome (SRS) who were epigenotyped. METHODS:This was a nonrandomized retrospective study with matched controls at a single center. Molecular analysis of 32 out of 37 GH-treated patients (16 females) revealed IGF2-H19 epimutatio...

    journal_title:Hormone research in paediatrics

    pub_type: 临床试验,杂志文章

    doi:10.1159/000354658

    authors: Binder G,Liebl M,Woelfle J,Eggermann T,Blumenstock G,Schweizer R

    更新日期:2013-01-01 00:00:00

  • Thyroid Sequelae of Pediatric Cancer Therapy.

    abstract::The hypothalamic-pituitary-thyroid axis is a common site of unintended, acquired disease either during or after the treatment of cancer. Children treated with external radiation therapy are at the highest risk for developing a thyroid-related late effect, but thyroid dysfunction and second primary thyroid neoplasms ca...

    journal_title:Hormone research in paediatrics

    pub_type: 杂志文章,评审

    doi:10.1159/000495040

    authors: Waguespack SG

    更新日期:2019-01-01 00:00:00

  • Pseudoisodicentric Xp chromosome [46,X,psu idic(X)(q21.1)] and its effect on growth and pubertal development.

    abstract:BACKGROUND:Most isodicentric (Xp) and (Xq) chromosomes occur as a mosaic with a 45,X cell line. Patients with a nonmosaic 46,X,idic(Xq) are rare. CASES:The first girl was referred at 13 years with a short stature and pubertal delay (M1, P2, A1). Her height was 141.6 cm (-3.1 SDS). Ovarian failure was present. The seco...

    journal_title:Hormone research in paediatrics

    pub_type: 杂志文章

    doi:10.1159/000357141

    authors: van der Kamp HJ,Kant SG,Ruivenkamp CA,Gijsbers AC,Haring D,Oostdijk W

    更新日期:2014-01-01 00:00:00

  • Evaluation of parathyroid gland function using sodium bicarbonate infusion test for 22q11.2 deletion syndrome.

    abstract:BACKGROUND/AIMS:22q11.2 Deletion syndrome is a congenital malformation syndrome with hypoparathyroidism. The spectrum of parathyroid gland dysfunction ranges from severe neonatal hypocalcemia to subclinical hypoparathyroidism. The parathyroid hormone (PTH) secretory reserve is reduced in a significant number of 22q11.2...

    journal_title:Hormone research in paediatrics

    pub_type: 杂志文章

    doi:10.1159/000315904

    authors: Nagasaki K,Iwasaki Y,Ogawa Y,Kikuchi T,Uchiyama M

    更新日期:2011-01-01 00:00:00

  • Auxological evaluation in patients with a 22q11.2 microdeletion syndrome: normal prevalence of obesity and neonatal length and gender influence on body mass index evolution.

    abstract:AIMS:To evaluate auxological parameters in children and adults with a 22q11.2 microdeletion syndrome (22q11.2 DS) and to compare prevalence of obesity to that in the French general population. METHODS:102 patients with 22q11.2 DS (49 males, 53 females) were recruited from birth to adulthood through a reference center ...

    journal_title:Hormone research in paediatrics

    pub_type: 杂志文章

    doi:10.1159/000328454

    authors: Reynaud R,Derain-Court J,Braunstein D,Veyrat M,Gaudart J,Giuliano F,Philip N

    更新日期:2011-01-01 00:00:00

  • MKRN3 mutations in familial central precocious puberty.

    abstract::Loss-of-function mutations in the gene encoding the makorin RING finger protein 3 (MKRN3) have recently been reported to underlie familial cases of central precocious puberty (CPP). The imprinted MKRN3 gene is expressed only from the paternal allele, and mutations inherited from the father affect boys and girls equall...

    journal_title:Hormone research in paediatrics

    pub_type: 杂志文章

    doi:10.1159/000362815

    authors: Schreiner F,Gohlke B,Hamm M,Korsch E,Woelfle J

    更新日期:2014-01-01 00:00:00

  • Identifying Cardiovascular Risk in Survivors of Childhood Leukaemia Treated with Haematopoietic Stem Cell Transplantation and Total Body Irradiation
.

    abstract:BACKGROUND:Survivors of childhood with haematopoietic stem cell transplantation and total body irradiation (HSCT/TBI) have an increased cardiometabolic risk without overt obesity. AIM:To describe cardiometabolic risk in HSCT/TBI survivors and identify anthropometric measurements of adiposity representative of cardiome...

    journal_title:Hormone research in paediatrics

    pub_type: 临床试验,杂志文章

    doi:10.1159/000455046

    authors: Wei C,Hunt L,Cox R,Bradley K,Elson R,Shield J,Stevens M,Crowne E

    更新日期:2017-01-01 00:00:00

  • Thyroid Ultrasound: More Sensitive than Radioactive Iodine Imaging in Detecting Recurrence of Papillary Thyroid Cancer in Two Pediatric Patients.

    abstract:BACKGROUND:Papillary thyroid cancer (PTC) is an uncommon pediatric disease with an excellent prognosis. In follow-up surveillance, neck ultrasound (US), basal and thyroid-stimulating hormone-stimulated serum thyroglobulin (Tg) levels, and diagnostic whole-body radioactive iodine scans (DxWBS) have been traditionally us...

    journal_title:Hormone research in paediatrics

    pub_type:

    doi:10.1159/000487436

    authors: Wise-Oringer BK,Goldis M,Regelmann MO,Klein M,Machac J,Kotlus Rosenberg H,Rapaport R

    更新日期:2018-01-01 00:00:00

  • Pituitary Antibodies in an Adolescent with Secondary Adrenal Insufficiency and Turner Syndrome.

    abstract:BACKGROUND/AIMS:Autoimmune hypophysitis (AH) is a rare inflammatory disease of the pituitary gland causing varying degrees of hypopituitarism and/or sellar compression. Cranial MRI remains the best noninvasive tool to diagnose AH, although a diagnosis of certainty requires pituitary biopsy. The objective of this study ...

    journal_title:Hormone research in paediatrics

    pub_type: 杂志文章

    doi:10.1159/000446912

    authors: Pollock AJ,Seibert TS,Salvatori C,Caturegli P,Allen DB

    更新日期:2017-01-01 00:00:00

  • Unusual virilization in girls with juvenile granulosa cell tumors of the ovary is related to intratumoral aromatase deficiency.

    abstract:BACKGROUND:Hyperandrogenism is a rare symptom of juvenile ovarian granulosa cell- tumors (JGCTO). This study aimed to determine whether hyperandrogenism was related to overexpression of SOX9, decreased expression of FOXL2 or absent aromatase expression in tumor with particular scheme of expression of P450scc and P450c1...

    journal_title:Hormone research in paediatrics

    pub_type: 杂志文章

    doi:10.1159/000313396

    authors: Kalfa N,Méduri G,Philibert P,Patte C,Boizet-Bonhoure B,Thibaut E,Pienkowski C,Jaubert F,Misrahi M,Sultan C

    更新日期:2010-01-01 00:00:00

  • A new horizon for glucose monitoring.

    abstract::Regular self-monitoring of blood glucose is crucial for proper insulin dosing and gives a reliable foundation for reasonable glycaemic control. According to recent data, recommended values for glycated haemoglobin A1c as set by the professional associations remain out of the reach for a large proportion of the paediat...

    journal_title:Hormone research in paediatrics

    pub_type: 杂志文章,评审

    doi:10.1159/000368924

    authors: Dovč K,Bratina N,Battelino T

    更新日期:2015-01-01 00:00:00

  • Techniques in pediatric surgery: congenital hyperinsulinism.

    abstract::For surgery in congenital hyperinsulinism (CHI), a distinct strategy and technique is required for focal, diffuse and atypical types. In focal CHI, a confined, localized and parenchyma-sparing resection which is guided by the PET-CT is always indicated in order to cure the patient. In diffuse CHI, however, the results...

    journal_title:Hormone research in paediatrics

    pub_type: 杂志文章

    doi:10.1159/000321902

    authors: Barthlen W,Mohnike W,Mohnike K

    更新日期:2010-01-01 00:00:00

  • Fast intraoperative testosterone assay confirms the location of an ovarian virilizing tumor in a young girl.

    abstract::The detection of testosterone-producing ovarian tumors in childhood and adolescence by imaging techniques only can be difficult because of the tumors' radiological structure and sometimes diminutive size. We describe an 11.5-year-old girl with a 9-month history of voice deepening, mild hirsutism, minor acne, increased...

    journal_title:Hormone research in paediatrics

    pub_type: 杂志文章

    doi:10.1159/000339683

    authors: Braun R,Peter A,Warmann S,Fuchs J,Binder G

    更新日期:2013-01-01 00:00:00

  • Endothelial nitric oxide synthase T(-786)C polymorphism in children and adolescents with type 1 diabetes and impaired endothelium-dependent dilatation.

    abstract:BACKGROUND/AIMS:This study aimed to investigate the association of endothelial nitric oxide synthase (eNOS) polymorphisms with impaired endothelium-dependent dilatation (EDD) in a cohort of children and adolescents with type 1 diabetes. METHODS:Ninety-seven children and adolescents with type 1 diabetes underwent ultra...

    journal_title:Hormone research in paediatrics

    pub_type: 杂志文章

    doi:10.1159/000329549

    authors: Battelino N,Sebestjen M,Keber I,Blagus R,Hovnik T,Bratina N,Battelino T

    更新日期:2011-01-01 00:00:00

  • The Association between Premature Adrenarche and Cardiovascular Risk May Be Greater than Expected.

    abstract:AIM:The aim of this study was to investigate the cardiovascular risk of children with premature adrenarche (PA). METHODS:A total of 75 children (44 with PA and 31 control subjects) aged 6-10 years were included in the study. Their metabolic, anthropometric, and echocardiographic parameters were recorded and compared. ...

    journal_title:Hormone research in paediatrics

    pub_type: 临床试验,杂志文章

    doi:10.1159/000452445

    authors: Çelik N,Alp H,Çamtosun E,Alp E,Çelik S,Berk E

    更新日期:2017-01-01 00:00:00

  • Correlation between Cosyntropin Stimulation Study and Disease Severity in Children with Fluid- and Catecholamine-Refractory Shock in the Pediatric and Cardiovascular Intensive Care Unit.

    abstract:BACKGROUND:The cosyntropin stimulation study (CSS) measures the patient's ability to adequately mount a cortisol response. Clinically, CSS results may not be used to guide hydrocortisone use. The objective of this study was to examine how the CSS results are associated with clinical parameters, mortality/disease severi...

    journal_title:Hormone research in paediatrics

    pub_type: 杂志文章

    doi:10.1159/000484561

    authors: Iyer P,Harrington B,Fadrowski JJ,Sibinga E,Amankwah EK

    更新日期:2018-01-01 00:00:00

  • Evaluation of vitamin D supplementation doses during pregnancy in a population at high risk for deficiency.

    abstract:AIM/BACKGROUND:Vitamin D supplementation during pregnancy is a well-accepted recommendation worldwide; however, the debate about the correct dose is ongoing. We aimed to compare daily doses of 600, 1,200, and 2,000 IU in this randomized, controlled study. METHODS:The study group consisted of 91 pregnant women aged 16-...

    journal_title:Hormone research in paediatrics

    pub_type: 杂志文章,随机对照试验

    doi:10.1159/000358833

    authors: Yesiltepe Mutlu G,Ozsu E,Kalaca S,Yuksel A,Pehlevan Y,Cizmecioglu F,Hatun S

    更新日期:2014-01-01 00:00:00

  • Central precocious puberty due to hypothalamic hamartomas correlates with anatomic features but not with expression of GnRH, TGFalpha, or KISS1.

    abstract:BACKGROUND/AIMS:Hypothalamic hamartomas are the most common identifiable cause of central precocious puberty (CPP). Hamartoma characteristics proposed to be associated with CPP include specific anatomic features and expression of molecules such as gonadotropin-releasing hormone (GnRH), transforming growth factor alpha ...

    journal_title:Hormone research in paediatrics

    pub_type: 杂志文章

    doi:10.1159/000308162

    authors: Chan YM,Fenoglio-Simeone KA,Paraschos S,Muhammad L,Troester MM,Ng YT,Johnsonbaugh RE,Coons SW,Prenger EC,Kerrigan JF Jr,Seminara SB

    更新日期:2010-01-01 00:00:00

  • Genetic variation in candidate genes like the HMGA2 gene in the extremely tall.

    abstract:BACKGROUND/AIMS:Genetic variation in several candidate genes has been associated with short stature. Recently, a high-mobility group A2 (HMGA2) gene SNP has been robustly associated with height in the general population. Only few have attempted to study these genes in extremely tall stature. We therefore studied common...

    journal_title:Hormone research in paediatrics

    pub_type: 杂志文章

    doi:10.1159/000330764

    authors: Hendriks AE,Brown MR,Boot AM,Oostra BA,Drop SL,Parks JS

    更新日期:2011-01-01 00:00:00

  • Marginal growth increase, altered bone quality and polycystic ovaries in female prepubertal rats after treatment with the aromatase inhibitor exemestane.

    abstract:BACKGROUND:Aromatase inhibition has been proposed as a potential approach for growth enhancement in children with short stature, but detailed animal studies are lacking. AIM:To assess the effect and potential adverse effects of aromatase inhibition on growth in female rats. METHODS:Prepubertal Wistar rats received in...

    journal_title:Hormone research in paediatrics

    pub_type: 杂志文章

    doi:10.1159/000271916

    authors: van Gool SA,Wit JM,De Schutter T,De Clerck N,Postnov AA,Kremer Hovinga S,van Doorn J,Veiga SJ,Garcia-Segura LM,Karperien M

    更新日期:2010-01-01 00:00:00

  • Age at menarche in childhood cancer survivors: results of a nationwide survey in Germany.

    abstract:BACKGROUND/AIMS:With rising cure rates of childhood cancer, side effects of treatment are attracting increasing interest. The present analysis evaluates the influence of tumor localization, radiotherapy and chemotherapy on the age of menarche. METHODS:4,689 former pediatric oncology patients, diagnosed 1980-2004, were...

    journal_title:Hormone research in paediatrics

    pub_type: 杂志文章

    doi:10.1159/000336688

    authors: Wessel T,Balcerek M,Reinmuth S,Hohmann C,Keil T,Henze G,Borgmann-Staudt A

    更新日期:2012-01-01 00:00:00

  • Is adrenocorticotropic hormone deficiency really rare in patients with idiopathic growth hormone deficiency and normal thyroid function tests?

    abstract:BACKGROUND/AIM:It was the aim of this study to evaluate subtle adrenocorticotropic hormone deficiencies in a group of patients with idiopathic growth hormone deficiency and without thyroid-stimulating hormone deficiency. METHODS:Growth hormone and cortisol responses to an insulin tolerance test of 25 patients (15 male...

    journal_title:Hormone research in paediatrics

    pub_type: 杂志文章

    doi:10.1159/000320479

    authors: Savas Erdeve S,Ocal G,Berberoglu M,Siklar Z,Hacihamdioglu B

    更新日期:2011-01-01 00:00:00