Catalano Antonino, Oliveri Cecilia, Natale Giuseppe, Agostino Rita Maria, Squadrito Giovanni, Gaudio Agostino, Gembillo Guido, Marina Djordje, Cernaro Valeria, Longhitano Elisa, Basile Giorgio, Morabito Nunziata, Santoro Domenico
Unit and School of Geriatrics, Department of Clinical and Experimental Medicine, University of Messina, Policlinico "G. Martino", 98124 Messina, Italy.
Mineral Metabolism and Nephrology Clinic of Vibo Valentia Hospital, 89900 Vibo Valentia, Italy.
J Clin Med. 2024 Oct 19;13(20):6239. doi: 10.3390/jcm13206239.
: Renal function influences bone metabolism, as kidney failure can increase the risk of fractures. Denosumab is an approved osteoporosis treatment, but its efficacy in relation to renal function has not yet been studied in real-life scenarios. This study aimed to investigate the denosumab-induced change in bone mineral density (BMD) according to kidney function. : A retrospective analysis was conducted at the outpatient clinic in postmenopausal women receiving denosumab (60 mg subcutaneously administered every 6 months). The glomerular filtration rate (eGFR) was measured by the 2021 CKD-EPI equation and patients were stratified for eGFR categories. BMD was measured by dual-energy X-ray absorptiometry. : 128 women (mean age 70.3 ± 9.4 years) were recruited. The mean denosumab treatment duration was 3.9 ± 1.4 years and all the participants had improved BMD values. In stepwise multiple regression analysis-after controlling for age, BMI, and treatment duration-the eGFR value (ß = -0.11, SE 0.04, = 0.01) was independently associated with the lumbar spine BMD change. The same association remained when the eGFR categories were considered (ß = 3.564, SE 1.29, = 0.007). In addition, after controlling for BMI and the duration of denosumab treatment, age (ß = -0.7915, SE 0.37, = 0.03) and eGFR (ß = -0.3257, SE 0.1567, = 0.04) were found to be associated with femoral neck BMD change. The association remained when considering eGFR categories (ß = 8.7339, SE 4.29, = 0.04). : This retrospective study suggests that eGFR is associated with denosumab efficacy in postmenopausal women treated for osteoporosis.
肾功能会影响骨代谢,因为肾衰竭会增加骨折风险。地诺单抗是一种已获批准的骨质疏松症治疗药物,但其在实际临床情况下与肾功能相关的疗效尚未得到研究。本研究旨在根据肾功能调查地诺单抗引起的骨密度(BMD)变化。:对接受地诺单抗治疗(每6个月皮下注射60mg)的绝经后女性门诊患者进行回顾性分析。采用2021年CKD-EPI方程测量肾小球滤过率(eGFR),并根据eGFR类别对患者进行分层。通过双能X线吸收法测量骨密度。:招募了128名女性(平均年龄70.3±9.4岁)。地诺单抗的平均治疗时长为3.9±1.4年,所有参与者的骨密度值均有所改善。在逐步多元回归分析中——在控制年龄、体重指数和治疗时长后——eGFR值(β=-0.11,标准误0.04,P=0.01)与腰椎骨密度变化独立相关。当考虑eGFR类别时,同样的关联仍然存在(β=3.564,标准误1.29,P=0.007)。此外,在控制体重指数和地诺单抗治疗时长后,发现年龄(β=-0.7915,标准误0.37,P=0.03)和eGFR(β=-0.3257,标准误0.1567,P=0.04)与股骨颈骨密度变化相关。当考虑eGFR类别时,这种关联仍然存在(β=8.7339,标准误4.29,P=0.04)。:这项回顾性研究表明,在接受骨质疏松症治疗的绝经后女性中,eGFR与地诺单抗疗效相关。