Gogas Yavuz Dilek, Aytürk Semra, Çetinkalp Şevki, Bayraktar Fırat, Kulaksızoğlu Mustafa, Hekimsoy Zeliha, Aydın Hasan, Uygur Melin, Deniz Ferhat, İpekçi Süleyman, Atmaca Ayşegül, Saraç Fulden, Özdemir Nilüfer, Cantürk Zeynep, Mert Meral, Sancak Seda, Ertörer Eda, Duran Cevdet, Akarsu Ersin, Deyneli Oğuzhan, Selek Alev, Gürlek Alper
Department of Endocrinology and Metabolism, Marmara University School of Medicine, İstanbul, Turkey.
Department of Endocrinology and Metabolism, Trakya University School of Medicine, Edirne, Turkey.
Eur J Rheumatol. 2021 Jul;8(3):156-161. doi: 10.5152/eurjrheum.2020.20139.
Paget disease of bone (PDB) is a metabolic bone disease that has been rarely reported in the Eastern countries. This study aimed to evaluate the clinical and demographic characteristics of patients with PDB followed up at endocrinology clinics in Turkey.
An invitation was sent to tertiary endocrinology clinics to complete a survey on the demographic, clinical, radiological, and laboratory parameters, as well as treatment modalities of patients with PDB. This study enrolled clinically and radiologically proven 185 patients with PDB from 18 endocrinology centers based in 10 cities of Turkey.
This cohort of PDB had female preponderance (women/men: 105/80) with a mean age, during diagnosis, of 57±10 years. Most of the patients (59.6%) were symptomatic at diagnosis. Bone pain and headache were the predominant clinical symptoms. Polyostotic disease was observed in 67.5% (n=125) of patients. Frequently affected bones were skull (41.6%), pelvis (53.5%), spine (41%), and femur (25.4%). Moreover, 17 patients with skull involvement had hearing loss. Mean serum alkaline phosphatase (ALP) level (552±652 IU/L; range: 280-5762 IU/L) was over the normal reference cutoff with normal serum calcium levels. Intravenous bisphosphonates (zoledronic acid, 5 mg; pamidronate, 60-90 mg) were the most used drugs (75%) for the treatment of PDB. Most of the patients (87.1%) treated with intravenous bisphosphonates responded well, with a decrease in serum ALP level (117±114 IU/L) in the 12th month of therapy. Furthermore, 16 patients relapsed after the second year of therapy; 3 patients did not respond to the initial intravenous bisphosphonate treatment.
The patients with PDB followed up by endocrinology clinics of Turkey exhibited polyostotic disease with classical clinical, radiological, and biochemical features and women's predominance with good response to intravenous bisphosphonate therapy.
骨Paget病(PDB)是一种代谢性骨病,在东方国家鲜有报道。本研究旨在评估在土耳其内分泌诊所接受随访的PDB患者的临床和人口统计学特征。
向三级内分泌诊所发出邀请,以完成一项关于PDB患者的人口统计学、临床、放射学和实验室参数以及治疗方式的调查。本研究纳入了来自土耳其10个城市的18个内分泌中心的185例经临床和放射学证实的PDB患者。
该PDB队列中女性占优势(女性/男性:105/80),诊断时的平均年龄为57±10岁。大多数患者(59.6%)在诊断时有症状。骨痛和头痛是主要的临床症状。67.5%(n=125)的患者观察到多骨型疾病。常见受累骨骼为颅骨(41.6%)、骨盆(53.5%)、脊柱(41%)和股骨(25.4%)。此外,17例颅骨受累患者有听力损失。平均血清碱性磷酸酶(ALP)水平(552±652 IU/L;范围:280 - 5762 IU/L)高于正常参考值下限,血清钙水平正常。静脉注射双膦酸盐(唑来膦酸,5 mg;帕米膦酸,60 - 90 mg)是治疗PDB最常用的药物(75%)。大多数接受静脉注射双膦酸盐治疗的患者(87.1%)反应良好,治疗第12个月时血清ALP水平下降(117±114 IU/L)。此外,16例患者在治疗第二年复发;3例患者对初始静脉注射双膦酸盐治疗无反应。
在土耳其内分泌诊所接受随访的PDB患者表现出多骨型疾病,具有典型的临床、放射学和生化特征,女性占优势,对静脉注射双膦酸盐治疗反应良好。