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骨骼生长人群中与低骨密度和儿童骨质疏松症相关的危险因素:一项横断面分析研究。

Risk factors associated with low bone mineral density and childhood osteoporosis in a population undergoing skeletal growth: a cross-sectional analytic study.

作者信息

Magallares Berta, Cerdá Dacia, Betancourt Jocelyn, Fraga Gloria, Park HyeSang, Codes-Méndez Helena, Quesada-Masachs Estefanía, López-Corbeto Mireia, Torrent Montserrat, Marín Ana, Herrera Silvia, Gich Ignasi, Boronat Susana, Casademont Jordi, Corominas Héctor, Malouf Jorge

机构信息

Department of Rheumatology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.

Department of Rheumatology, Universitari Dexeus-Grupo Quirón Salud Hospital, Barcelona, Spain.

出版信息

Front Endocrinol (Lausanne). 2025 May 23;16:1587985. doi: 10.3389/fendo.2025.1587985. eCollection 2025.

DOI:10.3389/fendo.2025.1587985
PMID:40487764
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12141024/
Abstract

BACKGROUND

Early identification of risk factors for low bone mass for chronological age (LBMca) and childhood osteoporosis (cOP) in patients undergoing skeletal growth is essential to mitigate long-term skeletal complications. cOP is diagnosed when LBMca (BMD Z-score ≤2) is accompanied by a clinically significant fracture history, or when vertebral fragility fractures are present.

METHODS

Patients under 21 years of age with at least one risk factor for LBMca (malabsorption syndrome, chronic inflammatory diseases, hematological diseases, endocrinopathies, drugs that affect bone metabolism, or insufficient calcium intake) were included. Data on fractures history and physical activity levels were collected. Spine and whole-body dual-energy x-ray absorptiometry (DXA) and vertebral morphometry were performed. Age-adjusted linear regression analysis evaluated associations between bone mineral density (BMD) and risk factors.

RESULTS

A total of 103 patients were included (mean age 9.8 years; 52.4% female), and 96.1% had more than two risk factors. The prevalence of LBMca was 10.5% and the prevalence of cOP was 4.8%. Vertebral BMD was positively associated with male sex. Whole body BMD was negatively associated with sedentary lifestyle and fracture history. Total body less head BMD showed negative associations with current steroid treatment, sedentary lifestyle, and history of fractures.

CONCLUSIONS

Pediatric populations at risk of LBMca or cOP often have multiple risk factors, notably modifying ones such as physical inactivity. Up to 10.5% of children with risk factors present LBMca and 4.8% have an undiagnosed or unknown cOP. Longitudinal studies are warranted to understand the long-term impact of the identified risk factors, including age, sex, sedentary lifestyle, ethnicity and vitamin D status, on bone health.

摘要

背景

在骨骼生长的患者中,早期识别按实足年龄计算的低骨量(LBMca)和儿童骨质疏松症(cOP)的风险因素对于减轻长期骨骼并发症至关重要。当LBMca(骨密度Z评分≤2)伴有具有临床意义的骨折病史,或存在椎体脆性骨折时,可诊断为cOP。

方法

纳入年龄在21岁以下且至少有一个LBMca风险因素(吸收不良综合征、慢性炎症性疾病、血液系统疾病、内分泌疾病、影响骨代谢的药物或钙摄入不足)的患者。收集骨折病史和身体活动水平的数据。进行脊柱和全身双能X线吸收测定(DXA)以及椎体形态测量。年龄调整线性回归分析评估骨密度(BMD)与风险因素之间的关联。

结果

共纳入103例患者(平均年龄9.8岁;52.4%为女性),96.1%的患者有两个以上风险因素。LBMca的患病率为10.5%,cOP的患病率为4.8%。椎体骨密度与男性性别呈正相关。全身骨密度与久坐不动的生活方式和骨折病史呈负相关。全身除头部外的骨密度与当前使用类固醇治疗、久坐不动的生活方式和骨折病史呈负相关。

结论

有LBMca或cOP风险的儿科人群通常有多种风险因素,尤其是如身体活动不足等可改变的因素。有风险因素的儿童中,高达10.5%存在LBMca,4.8%患有未诊断或未知的cOP。有必要进行纵向研究,以了解已确定的风险因素,包括年龄、性别、久坐不动的生活方式、种族和维生素D状态,对骨骼健康的长期影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8510/12141024/962605d3ee45/fendo-16-1587985-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8510/12141024/f08ba27a4e29/fendo-16-1587985-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8510/12141024/962605d3ee45/fendo-16-1587985-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8510/12141024/f08ba27a4e29/fendo-16-1587985-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8510/12141024/962605d3ee45/fendo-16-1587985-g002.jpg

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