Growth Charts for Shwachman-Diamond Syndrome at Ages 0 to 18 Years

被引:1
作者
Pegoraro, Anna [1 ]
Bezzerri, Valentino [1 ,2 ]
Tridello, Gloria [1 ]
Brignole, Cecilia [1 ]
Lucca, Francesca [1 ]
Pintani, Emily [1 ]
Danesino, Cesare [3 ]
Cesaro, Simone [4 ]
Fioredda, Francesca [5 ]
Cipolli, Marco [1 ]
机构
[1] Azienda Osped Univ Integrata, Cyst Fibrosis Ctr, I-37126 Verona, Italy
[2] Link Campus Univ, Dept Life Sci Hlth & Hlth Profess, I-00165 Rome, Italy
[3] Univ Pavia, Dept Mol Med, I-27100 Pavia, Italy
[4] Azienda Osped Univ Integrata, Pediat Hematol Oncol, I-37126 Verona, Italy
[5] IRCCS G Gaslini Hosp, Unit Hematol, I-16147 Genoa, Italy
关键词
Shwachman-Diamond syndrome; bone marrow failure; pancreatic insufficiency; ribosomopathy; CHILDREN; COHORT; RISK;
D O I
10.3390/cancers16071420
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary In this study, we drew up the growth charts of Italian patients with Shwachman-Diamond syndrome (SDS) at ages 0 to 18 years. We found that the 50th and 3rd percentiles of weight and height of the pediatric general population correspond to the 97th and 50th percentiles of patients with SDS, respectively. The median age at menarche in females with SDS was comparable with that of the general population. The percentage increment in weight of subjects aged 14-18 years was higher in patients with SDS than in the general population. This study provides insight into the potential usefulness of SDS-specific growth chart data as a resource for clinicians working with patients with SDS.Abstract Shwachman-Diamond syndrome (SDS) is one of the most common inherited bone marrow failure syndromes. SDS is characterized by hypocellular bone marrow, with a severe impairment of the myeloid lineage, resulting in neutropenia, thrombocytopenia, and, more rarely, anemia. Almost 15% of patients with SDS develop myelodysplastic syndrome or acute myeloid leukemia as early as childhood or young adulthood. Exocrine pancreatic insufficiency is another common feature of SDS. Almost all patients with SDS show failure to thrive, which is associated with skeletal abnormalities due to defective ossification. Considering these observations, it remains unfeasible to use the common growth charts already available for the general population. To address this issue, we report how we drew up growth charts of patients with SDS aged 0 to 18 years. We analyzed height, weight, and body max index (BMI) in 121 Italian patients with SDS. Results indicated that the 50th and 3rd percentiles of weight and height of the pediatric general population correspond to the 97th and 50th percentiles of patients with SDS aged 0-18 years, respectively. In addition, the percentage increment in weight of subjects aged 14-18 years was higher in patients with SDS than in the general population. SDS-specific growth charts, such as those described here, afford a new tool, which is potentially useful for both clinical and research purposes in SDS.
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页数:10
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