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重型β地中海贫血患儿异基因造血干细胞移植一年后的生长发育情况。

The growth and development of children with β-thalassemia major one year after allogeneic hematopoietic stem cell transplantation.

作者信息

Luo Hongfeng, Lin Yun, Kuang Caiyun

机构信息

Clinical Nutrition Department, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.

Data Research Center, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.

出版信息

Transl Pediatr. 2024 Nov 30;13(11):1972-1984. doi: 10.21037/tp-24-202. Epub 2024 Nov 26.

Abstract

BACKGROUND

Allogeneic hematopoietic stem cell transplantation (allo-HSCT) has proven to be an effective curative intervention for children with β-thalassemia major (β-TM). They are susceptible to growth disorders due various factors. The primary objective of this study was to investigate the growth and development of children with β-TM both before and after undergoing allo-HSCT during a one-year follow-up period.

METHODS

According to the international reference standards for child growth established by the World Health Organization in 2006, participants were divided into two groups based on their Z scores: weight-for-age Z scores (WAZ), height-for-age Z scores (HAZ), and body mass index-for-age Z scores (BAZ) before allo-HSCT. The first group included children with normal nutritional levels (-2≤ Z scores ≤2), while the second group consisted of children with malnutrition (Z scores <-2 or >2). Measurements of weight, height, and body mass index (BMI) were recorded at six time points: prior to allo-HSCT (T0), and 1 month (T1), 3 months (T3), 6 months (T6), 9 months (T9), and 12 months (T12) following the procedure.

RESULTS

Among the 56 children diagnosed with β-TM, 25% were malnourished prior to HSCT. In the group with normal nutrition, mean WAZ (P=0.04) and HAZ (P<0.001) values were significantly higher at T12 compared to T0; however, mean BAZ was similar at T12 and T0 (P=0.61). In contrast, in the malnutrition group, no significant differences were observed in mean WAZ (P=0.12), HAZ (P=0.27), or BAZ (P=0.75) values between T12 and T0. Notably, the incidence of increased HAZ was significantly more prevalent in children aged seven years or younger than in those older than seven years (P=0.01).

CONCLUSIONS

Children diagnosed with β-TM who had normal nutritional levels at the time of allo-HSCT showed significant growth improvements within one year of follow-up compared to their pre-transplantation state. Additionally, the age at which allo-HSCT was performed may substantially influence post-transplantation growth rates. Regular monitoring of growth and development from the time of diagnosis is crucial to ensure optimal nutritional status at the time of allo-HSCT, thereby enhancing the prognosis for these children after transplantation.

摘要

背景

异基因造血干细胞移植(allo-HSCT)已被证明是治疗重型β地中海贫血(β-TM)患儿的一种有效治愈性干预措施。由于多种因素,他们易患生长障碍。本研究的主要目的是在一年的随访期内,调查allo-HSCT前后重型β地中海贫血患儿的生长发育情况。

方法

根据世界卫生组织2006年制定的儿童生长国际参考标准,根据移植前的年龄别体重Z评分(WAZ)、年龄别身高Z评分(HAZ)和年龄别体重指数Z评分(BAZ)将参与者分为两组。第一组包括营养水平正常的儿童(-2≤Z评分≤2),而第二组由营养不良的儿童组成(Z评分<-2或>2)。在六个时间点记录体重、身高和体重指数(BMI):allo-HSCT前(T0),以及术后1个月(T1)、3个月(T3)、6个月(T6)、9个月(T9)和12个月(T12)。

结果

在56例诊断为重型β地中海贫血的儿童中,25%在造血干细胞移植前营养不良。在营养正常组中,T12时的平均WAZ(P=0.04)和HAZ(P<0.001)值显著高于T0;然而,T12和T0时的平均BAZ相似(P=0.61)。相比之下,在营养不良组中,T12和T0之间的平均WAZ(P=0.12)、HAZ(P=0.27)或BAZ(P=0.75)值没有显著差异。值得注意的是,7岁及以下儿童HAZ增加的发生率明显高于7岁以上儿童(P=0.01)。

结论

allo-HSCT时营养水平正常的重型β地中海贫血患儿在随访一年内的生长情况与移植前相比有显著改善。此外,进行allo-HSCT的年龄可能会对移植后的生长速度产生重大影响。从诊断时起定期监测生长发育对于确保allo-HSCT时的最佳营养状况至关重要,从而改善这些儿童移植后的预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9160/11621892/de39e9a1382c/tp-13-11-1972-f1.jpg

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