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Featured researches published by Hans Fors.


Pediatric Diabetes | 2008

Improved treatment satisfaction but no difference in metabolic control when using continuous subcutaneous insulin infusion vs. multiple daily injections in children at onset of type 1 diabetes mellitus

Lars Skogsberg; Hans Fors; Ragnar Hanas; John Eric Chaplin; Elisabeth Lindman; Josefin Skogsberg

Objective:  The aim of this study was to compare safety, metabolic control, and treatment satisfaction in children/adolescents at onset of type 1 diabetes mellitus who were treated with either continuous subcutaneous insulin infusion (CSII) or multiple daily injections (MDI).


Clinical Endocrinology | 2001

Currently used growth‐promoting treatment of children results in normal bone mass and density. A prospective trial of discontinuing growth hormone treatment in adolescents

Hans Fors; Ragnar Bjarnason; Lena Wirén; Kerstin Albertsson-Wikland; Ingvar Bosaeus; Bengt-Åke Bengtsson; Gudmundur Johannsson

BACKGROUND AND AIMS The need for continued GH replacement in patients with childhood‐onset GH deficiency (GHD) into adulthood has been recognized. The consequences of discontinuing GH treatment on bone mineralization in adolescent patients with GHD and short stature were examined over a period of 2 years.


Pediatric Physical Therapy | 2012

Bone health in children and adolescents with juvenile idiopathic arthritis and the influence of short-term physical exercise.

Eva Sandstedt; Anders Fasth; Hans Fors; Eva Beckung

Purpose: To study bone mineral density (BMD) in 54 children and adolescents with juvenile idiopathic arthritis before and after a short-term exercise program. Methods: Fifty-four children, 41 girls and 13 boys, median age 13.9 years, participated in a 12-week exercise program, with 33 children in an exercise group. The program consisted of one hundred 2-footed jumps with a rope and standardized muscle strength exercise. Both BMD and bone mineral content were assessed with dual-energy x-ray absorptiometry (DXA) and DXA Laser Calscan for the heel at the start and after 3 and 6 months. Results: The study group had BMD measurements within the reference range compared with normative data with Z score at start. Bone mineral density values in total body, but not Z score, increased significantly (P = .012) in the exercise group. Conclusions: The study group had BMD measurements within the reference range. Twelve weeks of exercise increases BMD in children with juvenile idiopathic arthritis.


The Journal of Clinical Endocrinology and Metabolism | 2008

Elevated Serum Levels of Estradiol, Dihydrotestosterone, and Inhibin B in Adult Males Born Small for Gestational Age

K. Allvin; Carina Ankarberg-Lindgren; Hans Fors; Jovanna Dahlgren

CONTEXT Prenatal growth restriction may affect future fertility in both females and males. Studies have shown that growth-retarded male rats have different sexual behavior and disturbed steroidogenesis. OBJECTIVE We hypothesized that adult human males born small for gestational age (SGA) have an altered sex hormone profile. DESIGN, SETTING, AND PATIENTS Twenty-five adult males born SGA with median birth weight -2.2 sd scores (SDS) and birth length -2.4 SDS were studied. Median age was 23.1 yr and final height -0.5 SDS. They were compared with 44 male controls with median age 20.5 yr and final height 0.4 SDS. MAIN OUTCOME MEASURE The primary outcome before the study started was 17beta-estradiol (E(2)) levels in SGA males. RESULTS The SGA group showed significantly higher median levels of E(2), 17.9 pg/ml (P < 0.001), and dihydrotestosterone (DHT), 0.543 ng/ml (P < 0.05), compared with controls, 12.6 pg/ml and 0.423 ng/ml, respectively. Testosterone (T) levels did not differ between groups. E(2) to T ratio correlated negatively to birth weight (r = -0.40, P < 0.01) and birth length (r = -0.44, P < 0.001). DHT to T ratio correlated negatively to birth weight (r = -0.51, P < 0.001) and birth length (r = -0.38, P < 0.01). Males born SGA also had significantly higher median levels of inhibin B, 164 pg/ml (P < 0.05), compared with controls, 137 pg/ml. Inhibin B correlated negatively to birth length (r = -0.34, P < 0.01). CONCLUSION SGA males of normal stature have higher levels of E(2), DHT, and inhibin B than controls, indicating a disturbed steroid synthesis or metabolism. Aromatase activity, calculated as E(2) to T ratio, and 5alpha-reductase activity, calculated as DHT to T ratio, is negatively correlated to size at birth.


Clinical Endocrinology | 2010

Metabolic outcome of GH treatment in prepubertal short children with and without classical GH deficiency

Ralph Decker; Kerstin Albertsson-Wikland; Berit Kriström; Andreas F. M. Nierop; Jan Gustafsson; Ingvar Bosaeus; Hans Fors; Zeev Hochberg; Jovanna Dahlgren

Context  Few studies have evaluated the metabolic outcomes of growth hormone (GH) treatment in idiopathic short stature (ISS). Moreover, children with ISS appear to need higher GH doses than children with GH deficiency (GHD) to achieve the same amount of growth and may therefore be at increased risk of adverse events during treatment. The individualized approach using prediction models for estimation of GH responsiveness, on the other hand, has the advantage of narrowing the range of growth response, avoiding too low or high GH doses.


Clinical Endocrinology | 2010

ORIGINAL ARTICLE: Metabolic outcome of GH treatment in prepubertal short children with and without classical GH deficiency

Ralph Decker; Kerstin Albertsson-Wikland; Berit Kriström; Andreas F. M. Nierop; Jan Gustafsson; Ingvar Bosaeus; Hans Fors; Zeev Hochberg; Jovanna Dahlgren

Context  Few studies have evaluated the metabolic outcomes of growth hormone (GH) treatment in idiopathic short stature (ISS). Moreover, children with ISS appear to need higher GH doses than children with GH deficiency (GHD) to achieve the same amount of growth and may therefore be at increased risk of adverse events during treatment. The individualized approach using prediction models for estimation of GH responsiveness, on the other hand, has the advantage of narrowing the range of growth response, avoiding too low or high GH doses.


Clinical Endocrinology | 2010

ORIGINAL ARTICLE: Metabolic outcome of GH treatment in prepubertal short children with and without classical GH deficiency: Dissociation of anabolic and lipolytic GH effects

Ralph Decker; Kerstin Albertsson-Wikland; Berit Kriström; Andreas F. M. Nierop; Jan Gustafsson; Ingvar Bosaeus; Hans Fors; Zeev Hochberg; Jovanna Dahlgren

Context  Few studies have evaluated the metabolic outcomes of growth hormone (GH) treatment in idiopathic short stature (ISS). Moreover, children with ISS appear to need higher GH doses than children with GH deficiency (GHD) to achieve the same amount of growth and may therefore be at increased risk of adverse events during treatment. The individualized approach using prediction models for estimation of GH responsiveness, on the other hand, has the advantage of narrowing the range of growth response, avoiding too low or high GH doses.


The Journal of Clinical Endocrinology and Metabolism | 1999

Serum Leptin Levels Correlate with Growth Hormone Secretion and Body Fat in Children

Hans Fors; Hisafumi Matsuoka; Ingvar Bosaeus; Sten Rosberg; Kerstin Albertsson Wikland; Ragnar Bjarnason


European Journal of Endocrinology | 2006

Bone mineral density and bone turnover in young adult survivors of childhood acute lymphoblastic leukaemia.

M Jarfelt; Hans Fors; B Lannering; Ragnar Bjarnason


European Journal of Endocrinology | 1999

Changes in body composition and leptin levels during growth hormone (GH) treatment in short children with various GH secretory capacities.

Hisafumi Matsuoka; Hans Fors; Ingvar Bosaeus; Sten Rosberg; Kerstin Albertsson-Wikland; Ragnar Bjarnason

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Ingvar Bosaeus

Sahlgrenska University Hospital

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Ragnar Bjarnason

Sahlgrenska University Hospital

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Ralph Decker

University of Gothenburg

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Zeev Hochberg

Technion – Israel Institute of Technology

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Sten Rosberg

University of Gothenburg

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