Bone turnover during inpatient nutritional therapy and outpatient follow-up in patients with anorexia nervosa compared with that in healthy control subjects

被引:0
作者
Heer, M
Mika, C
Grzella, I
Heussen, N
Herpertz-Dahlmann, B
机构
[1] Rhein Westfal TH Aachen, DLR, Inst Aerosp Med, D-51170 Cologne, Germany
[2] Rhein Westfal TH Aachen, Dept Child & Adolescent Psychiat, Cologne, Germany
[3] Elisabeth Clin Child & Adolescent Psychiat, Dortmund, Germany
[4] Rhein Westfal TH Aachen, Inst Med Stat, Fac Med, Aachen, Germany
关键词
adolescence; anorexia nervosa; nutritional therapy; weight gain; leptin; insulin-like growth factor I; IGF-I; bone turnover markers;
D O I
暂无
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Background: Osteopenia and osteoporosis are among the most frequent and severe complications in adolescents with anorexia nervosa. Objective: The aim of this study was to assess the influence of nutritional therapy on bone metabolism during adolescent anorexia nervosa. Design: We studied 19 anorectic patients aged 14.1 +/- 1.4 y((x) over bar +/- SD) with a body mass index (BMI; in kg/m(2)) of 14.2 +/- 1.4 and 19 age-matched control subjects aged 15.1 +/- 2.3 y with a BMI of 20.8 +/- 1.9 for 1 y. Blood samples were taken for the measurement of bone markers, insulin-like growth factor I (IGF-I), and leptin. Results: BMI rose significantly from 14.2 1.4 at baseline to 17.4 +/- 0.6 (P < 0.0001) at week 15. Compared with concentrations in the control subjects, concentrations of the bone formation markers procollagen type I propeptide (PICP) and bone alkaline phosphatase (bAP) in the anorectic patients were lower at baseline (PICP: P = 0.0071; bAP: P = 0.0012), increased with nutritional therapy (PICP: P = 0.0060, bAP: P = 0.0147), and were no longer significantly different (P > 0.05) during the follow-up period. Concentrations of IGF-I and leptin were significantly lower (P < 0.0001 for both) in the anorectic patients than in the control subjects at baseline. IGF-I increased with nutritional therapy but was still significantly lower (P = 0.0036) than that in the control group and decreased again during the follow-up period (P = 0.0126). In contrast, serum C-telopeptide decreased with nutritional therapy (P = 0.0446). Conclusion: Nutritional therapy improves concentrations of bone formation markers in adolescent patients with anorexia nervosa.
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页码:774 / 781
页数:8
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共 58 条
[1]  
Amling M, 2001, ADV EXP MED BIOL, V496, P85
[2]   Leptin: factor in the central nervous system regulation of bone mass. Development of a new understanding of bone remodeling, skeletal reconstruction, skeletal preservation, and skeletal repair [J].
Amling, M ;
Schilling, AF ;
Haberland, M ;
Rueger, JM .
ORTHOPADE, 2001, 30 (07) :418-424
[3]  
Amling M, 2000, BIOESSAYS, V22, P970
[4]   SUPPLEMENTATION TRIALS WITH CALCIUM CITRATE MALATE - EVIDENCE IN FAVOR OF INCREASING THE CALCIUM RDA DURING CHILDHOOD AND ADOLESCENCE [J].
ANDON, MB ;
LLOYD, T ;
MATKOVIC, V .
JOURNAL OF NUTRITION, 1994, 124 (08) :S1412-S1417
[5]   Calcium accretion in girls and boys during puberty: A longitudinal analysis [J].
Bailey, DA ;
Heather, ADM ;
McKay, HA ;
Whiting, S ;
Mirwald, R .
JOURNAL OF BONE AND MINERAL RESEARCH, 2000, 15 (11) :2245-2250
[6]   Hypothalamic Y2 receptors regulate bone formation [J].
Baldock, PA ;
Sainsbury, A ;
Couzens, M ;
Enriquez, RF ;
Thomas, GP ;
Gardiner, EM ;
Herzog, H .
JOURNAL OF CLINICAL INVESTIGATION, 2002, 109 (07) :915-921
[7]  
Baranowska B, 2001, NEUROENDOCRINOL LETT, V22, P356
[8]   CRITICAL YEARS AND STAGES OF PUBERTY FOR SPINAL AND FEMORAL BONE MASS ACCUMULATION DURING ADOLESCENCE [J].
BONJOUR, JP ;
THEINTZ, G ;
BUCHS, B ;
SLOSMAN, D ;
RIZZOLI, R .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1991, 73 (03) :555-563
[9]   Compromised bone density 11.4 years after diagnosis of anorexia nervosa [J].
Brooks, ER ;
Ogden, BW ;
Cavalier, DS .
JOURNAL OF WOMENS HEALTH, 1998, 7 (05) :567-574
[10]   Weight gain reverses bone turnover and restores circadian variation of bone resorption in anorexic patients [J].
Caillot-Augusseau, A ;
Lafage-Proust, MH ;
Margaillan, P ;
Vergely, N ;
Faure, S ;
Paillet, S ;
Lang, F ;
Alexandre, C ;
Estour, B .
CLINICAL ENDOCRINOLOGY, 2000, 52 (01) :113-121