Prevention and Treatment of Glucocorticoid-Induced Osteoporosis in adults: Recommendations From the European Calcified Tissue Society.

IF 5.3 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM European Journal of Endocrinology Pub Date : 2024-11-18 DOI:10.1093/ejendo/lvae146
Julien Paccou, Maria P Yavropoulou, Anda Mihaela Naciu, Manju Chandran, Osvaldo D Messina, Tim Rolvien, John J Carey, Stella D'oronzo, Athanasios D Anastasilakis, Kenneth G Saag, Willem F Lems
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Abstract

Introduction: This report presents the recommendations of the European Calcified Tissue Society (ECTS) for the prevention and treatment of glucocorticoid-induced osteoporosis (GIOP) in adults. Our starting point was that the recommendations be evidence based, focused on non-bone specialists who treat patients with GC and broadly supported by ECTS.

Methods: The recommendations were developed by global experts. After a comprehensive review of the literature, twenty-five recommendations were formulated, based on quality evidence. For stratifying fracture risk and the most appropriate first line of treatment, we have classified patients into 3 categories: those at medium risk of fractures i.e. adults without a recent (in the last 2 years) history of fracture, those at high risk of fractures i.e. adults with recent history of fracture, and/or at least one vertebral fracture (grade ≥ 2 according to Genant classification), and those at very high risk of fractures i.e. adults aged ≥ 70 years with a recent hip fracture, pelvis fracture, and/or at least one vertebral fracture (grade ≥ 2 according to Genant classification) . The subtopics in the recommendations include Who to assess, How to assess, Who to treat, How to treat, and Follow-up and Monitoring.

Results: General measures are recommended for all patients who are being prescribed glucocorticoids (GCs) for > 3 months: i.e. calcium and protein intake should be normalized, a 25(OH) vitamin D concentration of 50-125 nmol/L should be attained, and the risk of falls be minimized. 1)Who to assess? (R1-2) A preliminary assessment of fracture risk should be routinely performed in patients likely to receive oral GCs for ≥ 3 months: (i) women and men ≥ 50 years and (ii) patients at increased risk of fracture (history of fragility fracture and/or have comorbidities or are on medications that are frequently associated with osteoporosis.2)How to assess (fracture risk)? (R3-6) Clinical risk factors including history of fragility fracture, systematic vertebral imaging, and GCs dose-adjusted FRAX, measurement of BMD by DXA, fall risk, and biochemical testing.3) Who to treat? (R7-12) Anti-osteoporosis treatment is indicated for women and men ≥ 50 years with (i) the presence of a recent history of vertebral and/or non-vertebral fracture (less than 2 years) (ii)and/or a GCs dosage ≥ 7.5 mg/day, (iii)and/or age ≥ 70 years (iv)and/or a T-score ≤ -1.5, (v)and/or 10-year probability risk above the country specific GC dose-adjusted FRAX® thresholds. In premenopausal women and men < 50 years with a Z-score ≤ -2 and/or a history of fragility fracture, it is recommended to refer the patient to a bone specialist.4) How to treat? (R13-18) In women and men ≥ 50 years, (i) alendronate or risedronate is preferred as the first line of treatment in patients at medium risk of fractures, (ii) zoledronic acid or denosumab in patients at high risk of fractures, and (iii) teriparatide in patients at very high risk of fractures. It is imperative that sequential therapy be implemented in individuals receiving denosumab or teriparatide as their first-line treatment regimen.5) Follow-up and Monitoring (R19-25): In patients receiving anti-osteoporosis treatment, monitoring of clinical risk factors (e.g., history of fragility fracture), systematic vertebral imaging, fall risk, BMD measurement using DXA, and biochemical testing should be performed regularly during follow-up.

Conclusions: The new, evidence-based recommendations by the ECTS for the prevention and treatment of GIOP provide clear and pragmatic advice to all health practitioners especially those who are not bone specialists.

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预防和治疗糖皮质激素诱发的成人骨质疏松症:欧洲钙化组织协会的建议。
导言:本报告介绍了欧洲钙化组织协会(ECTS)对预防和治疗糖皮质激素诱导的成人骨质疏松症(GIOP)的建议。我们的出发点是这些建议以证据为基础,以治疗糖皮质激素患者的非骨科专家为重点,并得到欧洲钙化组织学会的广泛支持:方法:建议由全球专家制定。方法:建议由全球专家制定。在对文献进行全面审查后,根据高质量的证据制定了 25 项建议。为了对骨折风险和最合适的一线治疗进行分层,我们将患者分为三类:中度骨折风险患者,即近期(近两年内)无骨折史的成年人;高度骨折风险患者,即近期有骨折史的成年人;以及中度骨折风险患者,即近期有骨折史的成年人。骨折高危人群,即近期有骨折史和/或至少有一处椎体骨折的成年人(根据吉南特分类法,等级≥2),以及骨折高危人群,即年龄≥70 岁、近期有髋部骨折、骨盆骨折和/或至少有一处椎体骨折的成年人(根据吉南特分类法,等级≥2)。建议中的副标题包括评估对象、如何评估、治疗对象、如何治疗以及随访和监测:结果:建议对所有使用糖皮质激素(GCs)超过3个月的患者采取一般措施:即钙和蛋白质摄入量应恢复正常,25(OH)维生素D浓度应达到50-125 nmol/L,跌倒风险应降至最低。1)对谁进行评估?(R1-2)对于可能口服 GCs≥ 3 个月的患者,应常规进行骨折风险初步评估:(i) 年龄≥ 50 岁的女性和男性;(ii) 骨折风险增加的患者(有脆性骨折史和/或有合并症或正在服用常与骨质疏松症相关的药物)。(建议 3-6)临床风险因素,包括脆性骨折史、系统的椎体成像和 GCs 剂量调整的 FRAX、通过 DXA 测量 BMD、跌倒风险和生化检测。(R7-12)抗骨质疏松症治疗适用于年龄≥50岁的女性和男性,(i)近期有椎体和/或非椎体骨折史(少于2年),(ii)和/或GCs剂量≥7.5毫克/天,(iii)和/或年龄≥70岁,(iv)和/或T评分≤-1.5,(v)和/或10年概率风险高于特定国家GCs剂量调整FRAX®阈值。对于 Z 评分≤-2 和/或有脆性骨折史的绝经前女性和年龄小于 50 岁的男性,建议将患者转诊至骨科专家。(R13-18)对于年龄≥50岁的女性和男性,(i) 对于骨折风险中等的患者,首选阿仑膦酸钠或利塞膦酸钠作为一线治疗药物;(ii) 对于骨折风险高的患者,首选唑来膦酸或地诺单抗;(iii) 对于骨折风险极高的患者,首选特立帕肽。5) 随访和监测(R19-25):对于接受抗骨质疏松症治疗的患者,在随访期间应定期监测临床风险因素(如脆性骨折史)、系统性椎体成像、跌倒风险、使用 DXA 测量 BMD 以及生化检测:ECTS 就 GIOP 的预防和治疗提出了以证据为基础的新建议,为所有医疗从业人员(尤其是非骨科专家)提供了明确而实用的建议。
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来源期刊
European Journal of Endocrinology
European Journal of Endocrinology 医学-内分泌学与代谢
CiteScore
9.80
自引率
3.40%
发文量
354
审稿时长
1 months
期刊介绍: European Journal of Endocrinology is the official journal of the European Society of Endocrinology. Its predecessor journal is Acta Endocrinologica. The journal publishes high-quality original clinical and translational research papers and reviews in paediatric and adult endocrinology, as well as clinical practice guidelines, position statements and debates. Case reports will only be considered if they represent exceptional insights or advances in clinical endocrinology. Topics covered include, but are not limited to, Adrenal and Steroid, Bone and Mineral Metabolism, Hormones and Cancer, Pituitary and Hypothalamus, Thyroid and Reproduction. In the field of Diabetes, Obesity and Metabolism we welcome manuscripts addressing endocrine mechanisms of disease and its complications, management of obesity/diabetes in the context of other endocrine conditions, or aspects of complex disease management. Reports may encompass natural history studies, mechanistic studies, or clinical trials. Equal consideration is given to all manuscripts in English from any country.
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