Igarashi Shun, Kasukawa Yuji, Nozaka Koji, Tsuchie Hiroyuki, Abe Kazunobu, Saito Hikaru, Shoji Ryo, Kasama Fumihito, Harata Shuntaro, Okamoto Kento, Oya Keita, Miyakoshi Naohisa
Department of Orthopedic Surgery, Akita University Graduate School of Medicine, 1-1-1, Hondo, Akita, 010-8543, Japan.
Department of Rehabilitation Medicine, Akita University Hospital, 1-1-1, Hondo, Akita, 010-8543, Japan.
Osteoporos Sarcopenia. 2023 Dec;9(4):121-130. doi: 10.1016/j.afos.2023.11.002. Epub 2023 Dec 21.
Chronic kidney disease (CKD) complicated by secondary hyperparathyroidism (SHPT) is associated with an increased risk of fragility fractures. Etelcalcetide (EC) is a treatment for SHPT that reduces serum parathyroid hormone (PTH) levels. However, the effects of combined treatment with osteoporosis drugs such as teriparatide (TPTD) remain unclear. This study investigates the combined effects of EC and TPTD on bone in CKD model rats.
The CKD model was established in 8-week-old male Wistar rats by feeding them a 0.75% adenine diet for 4 weeks. At 20 weeks of age, the rats were divided into 4 groups (N = 9-10 in each group): CKD group (vehicle administration), TPTD group (30 μg/kg, 3 times/week), EC group (0.6 mg/kg, daily), and Comb group (TPTD and EC combined). EC was injected for 12 weeks starting at 20 weeks of age, and TPTD was injected for 8 weeks starting at 24 weeks of age. After treatment, the followings were evaluated: bone mineral density, bone strength, biochemical tests, bone and fat histomorphometry, and micro-computed tomography.
In CKD model rats, the combination of EC and TPTD was more effective in increasing cortical bone thickness and bone strength and inhibiting porosity. In addition, the combined treatment decreased bone marrow adiposity and fibrosis, and it increased bone mass and improved bone microstructure in trabecular bone.
With the observed benefits such as improved bone mass, bone strength, structural properties, and bone marrow adiposity, combination therapy may be a potential way to improve bone fragility in CKD.
慢性肾脏病(CKD)合并继发性甲状旁腺功能亢进(SHPT)与脆性骨折风险增加相关。依特卡肽(EC)是一种治疗SHPT的药物,可降低血清甲状旁腺激素(PTH)水平。然而,与特立帕肽(TPTD)等骨质疏松药物联合治疗的效果仍不明确。本研究探讨EC和TPTD联合应用对CKD模型大鼠骨骼的影响。
8周龄雄性Wistar大鼠通过喂食0.75%腺嘌呤饮食4周建立CKD模型。在20周龄时,将大鼠分为4组(每组n = 9 - 10):CKD组(给予赋形剂)、TPTD组(30μg/kg,每周3次)、EC组(0.6mg/kg,每日)和联合组(TPTD与EC联合)。从20周龄开始注射EC,持续12周,从24周龄开始注射TPTD,持续8周。治疗后,评估以下指标:骨密度、骨强度、生化检测、骨与脂肪组织形态计量学以及微型计算机断层扫描。
在CKD模型大鼠中,EC与TPTD联合应用在增加皮质骨厚度和骨强度以及抑制孔隙率方面更有效。此外,联合治疗减少了骨髓脂肪化和纤维化,并增加了骨量,改善了小梁骨微结构。
鉴于观察到联合治疗具有改善骨量、骨强度、结构特性以及骨髓脂肪化等益处,联合治疗可能是改善CKD患者骨脆性的一种潜在方法。