Chan Kevin, Karaboyas Angelo, Morgenstern Hal, Robinson Bruce M, Port Friedrich K, Jacobson Stefan H, Fukagawa Masafumi, Meier Yvonne, Csomor Philipp A, Pisoni Ronald L
Division of Nephrology, Massachusetts General Hospital, Boston, MA.
Arbor Research Collaborative for Health, University of Michigan Medical School, Ann Arbor, MI.
Kidney Med. 2019 May 10;1(3):86-96. doi: 10.1016/j.xkme.2019.04.004. eCollection 2019 May-Jun.
RATIONALE & OBJECTIVE: Normalization of parathyroid hormone (PTH), serum calcium, and phosphorus levels may prevent coronary and bone disease in hemodialysis (HD) patients. We describe the trajectory of these mineral bone disorder parameters and treatments during the first 5 years of HD by international region and race.
Prospective cohort study.
SETTING & PARTICIPANTS: 33,517 US black/African American, US non-black/African American, European, and Japanese HD patients from the Dialysis Outcomes and Practice Patterns Study (DOPPS) phases 4 to 5 (2009-2015).
Time since HD initiation.
Monthly cross-sections of mineral bone disorder parameters (PTH, serum calcium, and phosphorus) and medications (cinacalcet, active vitamin D, and phosphate binders).
Mean PTH levels declined precipitously during the first 4 months of HD in all 4 groups, then steadily increased during the next 4.5 years in the United States/Europe but not in Japan. 3 years after HD initiation (month 36), mean PTH level was highest in US black/African Americans (496 pg/mL), despite greater prescription of cinacalcet (23%) and active vitamin D (85%), and lowest in Japan (151 pg/mL). Mean serum calcium and phosphorus levels increased during the first 4 months of HD. By month 36, the mean calcium level was lower in Japan (8.8 mg/dL) than United States/Europe (9.0-9.1 mg/dL), while the mean phosphorus level was lower in Europe (4.8 mg/dL) than United States/Japan (5.1-5.3 mg/dL).
Lack of data for medication dosages; most patients were not followed from HD onset.
Large differences exist in the levels, trajectories, and therapies for PTH, calcium, and phosphorus by country and race in the first 5 years of HD. Higher PTH levels were observed in the United States, especially among black/African American patients, despite greater use of cinacalcet and active vitamin D than in Japan or Europe. Potential contributors to differences in PTH levels should be explored to study their impact on PTH management strategies and consequent bone and cardiovascular complications.
甲状旁腺激素(PTH)、血清钙和磷水平的正常化可能预防血液透析(HD)患者的冠状动脉疾病和骨病。我们按国际区域和种族描述了HD开始后前5年这些矿物质骨代谢紊乱参数及治疗的变化轨迹。
前瞻性队列研究。
来自透析预后与实践模式研究(DOPPS)第4至5阶段(2009 - 2015年)的33517名美国黑人/非裔美国人、美国非黑人/非裔美国人、欧洲人和日本HD患者。
HD开始后的时间。
矿物质骨代谢紊乱参数(PTH、血清钙和磷)及药物(西那卡塞、活性维生素D和磷结合剂)的月度横断面数据。
所有4组患者的平均PTH水平在HD开始后的前4个月急剧下降,随后在美国/欧洲的接下来4.5年中稳步上升,但在日本没有。HD开始3年后(第36个月),美国黑人/非裔美国人的平均PTH水平最高(496 pg/mL),尽管西那卡塞(23%)和活性维生素D(85%)的处方量更大,而日本最低(151 pg/mL)。HD开始后的前4个月,平均血清钙和磷水平升高。到第36个月时,日本的平均钙水平(8.8 mg/dL)低于美国/欧洲(9.0 - 9.1 mg/dL),而欧洲的平均磷水平(4.8 mg/dL)低于美国/日本(5.1 - 5.3 mg/dL)。
缺乏药物剂量数据;大多数患者并非从HD开始就进行随访。
HD开始后的前5年,不同国家和种族在PTH、钙和磷的水平、变化轨迹及治疗方面存在很大差异。在美国观察到较高的PTH水平,尤其是在黑人/非裔美国患者中,尽管美国使用西那卡塞和活性维生素D的比例高于日本或欧洲。应探究导致PTH水平差异的潜在因素,以研究它们对PTH管理策略以及随之而来的骨和心血管并发症的影响。