Polgreen L E, Rudser K, Deyo M, Smith A, Baker K S, Petryk A
Division of Endocrinology, Department of Pediatrics, University of Minnesota, Minneapolis, MN 55454, USA.
Pediatr Transplant. 2012 Dec;16(8):852-7. doi: 10.1111/j.1399-3046.2012.01780.x. Epub 2012 Aug 20.
Bone loss has been observed within the first six months after HCT in both children and adults. While there is some evidence that bone formation may be reduced in children after HCT, it is currently unknown whether bone resorption is increased. The objective of this prospective study was to evaluate changes in markers of bone resorption over the first six months after pediatric HCT. Twenty-six participants (eight females) aged 10.9 ± 3.4 yr entered the study prior to HCT. Bone resorption was measured by urine DPD and PYD, and by plasma NTX and CTX. Seventeen participants who completed day +30 visit and either day +100 or +180 visits were included in the analysis. DPD increased between days +30 and +100 (mean change, 11.3 nmol/nmol creatinine; p = 0.012) and between days +30 and +180 (13.7 nmol/nmol creatinine; p = 0.036). PYD increased between days +30 and +100 (32 nmBCE/L; p = 0.019). CTX increased between baseline and day +100 (5.9 μg/L; p = 0.012). Changes in NTX levels were not statistically significant. This study shows that markers of bone resorption increase in children after HCT, suggesting that increased resorption may be a contributing factor to the pathophysiology of bone loss after pediatric HCT.
在儿童和成人造血干细胞移植(HCT)后的头六个月内均观察到骨质流失。虽然有一些证据表明儿童造血干细胞移植后骨形成可能减少,但目前尚不清楚骨吸收是否增加。这项前瞻性研究的目的是评估小儿造血干细胞移植后头六个月内骨吸收标志物的变化。26名年龄为10.9±3.4岁的参与者(8名女性)在造血干细胞移植前进入研究。通过尿脱氧吡啶啉(DPD)和吡啶啉(PYD)以及血浆N-端肽(NTX)和I型胶原C-端肽(CTX)来测量骨吸收。17名完成了第30天随访以及第100天或第180天随访的参与者被纳入分析。DPD在第30天至第100天之间增加(平均变化为11.3 nmol/nmol肌酐;p = 0.012),在第30天至第180天之间增加(13.7 nmol/nmol肌酐;p = 0.036)。PYD在第30天至第100天之间增加(32 nmBCE/L;p = 0.019)。CTX在基线至第100天之间增加(5.9 μg/L;p = 0.012)。NTX水平的变化无统计学意义。这项研究表明,儿童造血干细胞移植后骨吸收标志物增加,提示吸收增加可能是小儿造血干细胞移植后骨质流失病理生理过程的一个促成因素。