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Bone mass and biomarkers in young women with anorexia nervosa: a prospective 3-year follow-up study
Univ Gothenburg, Sweden; Sahlgrens Univ Hosp, Sweden.
Univ Gothenburg, Sweden.
Univ Gothenburg, Sweden.
Univ Gothenburg, Sweden.
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2022 (English)In: Journal of Bone and Mineral Metabolism, ISSN 0914-8779, E-ISSN 1435-5604, Vol. 40, no 6, p. 974-989Article in journal (Refereed) Published
Abstract [en]

Introduction Anorexia nervosa (AN) increases the risk of impaired bone health, low areal bone mineral density (aBMD), and subsequent fractures. This prospective study investigated the long-term effects of bone and mineral metabolism on bone and biomarkers in 22 women with AN. Materials and methods Body composition and aBMD were measured by dual-energy X-ray absorptiometry (DXA) and peripheral quantitative computed tomography. Total and free 25-hydroxyvitamin D (25OHD), C-terminal collagen cross-links (CTX), osteocalcin, bone-specific alkaline phosphatase (BALP), leptin, sclerostin, and oxidized/non-oxidized parathyroid hormone (PTH) were analyzed before and after 12 weeks of intensive nutrition therapy and again 3 years later. An age-matched comparison group of 17 healthy women was recruited for the 3-year follow-up. Results Body mass index (BMI) and fat mass increased from baseline to 3 years in women with AN. Sclerostin decreased during nutrition therapy and further over 3 years, indicating reduced bone loss. CTX was elevated at baseline and after 12 weeks but decreased over 3 years. BALP increased during nutrition therapy and stabilized over 3 years. Free 25OHD was stable during treatment but decreased over 3 years. Non-oxidized PTH was stable during treatment but increased over 3 years. Trabecular volumetric BMD in AN patients decreased during the first 12 weeks and over 3 years despite stable BMI and bone biomarkers implying increased BMD. Conclusion Our findings highlight the importance of early detection and organized long-term follow-up of bone health in young women with a history of AN.

Place, publisher, year, edition, pages
SPRINGER , 2022. Vol. 40, no 6, p. 974-989
Keywords [en]
Eating disorder; Sclerostin; DXA; Osteoporosis; Vitamin D
National Category
Orthopaedics
Identifiers
URN: urn:nbn:se:liu:diva-187869DOI: 10.1007/s00774-022-01359-xISI: 000840016400001PubMedID: 35960382Scopus ID: 2-s2.0-85135825585OAI: oai:DiVA.org:liu-187869DiVA, id: diva2:1691776
Note

Funding Agencies|Queen Silvia Childrens Hospital Research Foundation; ALF grants from Region ostergotland; Capio Foundation; Samariten Foundation; HKH Princess Lovisas Foundation; Sahlgrenska University Hospital; Health and Medical Care Committee of the Regional Executive Board of Region Vastra Gotaland; Swedish government and the county council [ALFGBG-716831, 678871, 965009, 117661]

Available from: 2022-08-31 Created: 2022-08-31 Last updated: 2023-03-20

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Division of Clinical Chemistry and PharmacologyFaculty of Medicine and Health SciencesDepartment of Clinical Chemistry
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