Kuvibidila Solo R, Gardner Renée, Velez Maria, Warrier Raj
Department of Pediatrics, Louisiana State University Health Sciences Center, New Orleans, LA.
The University of Queensland School of Medicine, Ochsner Clinical School, New Orleans, LA.
Ochsner J. 2018 Winter;18(4):308-317. doi: 10.31486/toj.17.0044.
Children with sickle cell disease (SCD) often have infections, growth deficits, and impaired immunity, problems that also are observed in individuals with a vitamin A deficiency (plasma retinol concentration <20 μg/dL). The goal of this study was to investigate the association between vitamin A, health status, and the in vitro immune function of children with SCD.
Fifty-nine children (40 SS, 11 SC, and 8 Sβ [Sβ] hemoglobin genotypes) 9 months to 18 years old were investigated for plasma levels of retinol, retinol binding protein, C-reactive protein, alpha-1-acid glycoprotein, lymphocyte proliferation, and interleukin (IL)-2 activity in supernatant of phytohemagglutinin-treated lymphocytes.
The plasma retinol concentrations of children with SCD (mean 57.6 μg/dL, range 4.6-116 μg/dL) were not different from those of 21 normal individuals (mean 62 μg/dL, range 28.7-162 μg/dL). Plasma retinol concentrations did not vary by hemoglobin genotype but were lower in boys than in girls ( < 0.05) and were also lower in children with inflammation ( = 0.1). Seven children (11.9%) (6 HbSS, 1 HbSβ) were vitamin A-deficient, and 9 children (15.3%) had suboptimal vitamin A status (plasma retinol concentration of 20-29 μg/dL). Children with vitamin A deficiency had slightly lower height ( = 0.09) and weight mean percentiles, lymphocyte proliferative responses, and IL-2 activity ( > 0.1), but higher means of C-reactive protein ( = 0.05), pain crisis episodes and inflammation ( = 0.1), and health scores ( > 0.1) than children who were not vitamin A-deficient. Lymphocyte proliferative responses negatively correlated with health score, pain crisis episodes, and blood units received, but positively correlated with retinol binding protein ( < 0.05 to = 0.1).
Identification and correction of suboptimal vitamin A status in children with SCD may improve immunity and attenuate certain health complications associated with this disease.
镰状细胞病(SCD)患儿常出现感染、生长发育迟缓及免疫功能受损等问题,这些问题在维生素A缺乏(血浆视黄醇浓度<20μg/dL)的个体中也有观察到。本研究的目的是调查维生素A、健康状况与SCD患儿体外免疫功能之间的关联。
对59名9个月至18岁的儿童(40名SS型、11名SC型和8名Sβ[Sβ]血红蛋白基因型)进行了研究,检测其血浆视黄醇、视黄醇结合蛋白、C反应蛋白、α-1-酸性糖蛋白水平,以及植物血凝素处理的淋巴细胞上清液中的淋巴细胞增殖和白细胞介素(IL)-2活性。
SCD患儿的血浆视黄醇浓度(平均57.6μg/dL,范围4.6 - 116μg/dL)与21名正常个体(平均62μg/dL,范围28.7 - 162μg/dL)的血浆视黄醇浓度无差异。血浆视黄醇浓度不因血红蛋白基因型而异,但男孩低于女孩(<0.05),炎症患儿也较低(=0.1)。7名儿童(11.9%)(6名HbSS型、1名HbSβ型)维生素A缺乏,9名儿童(15.3%)维生素A状态欠佳(血浆视黄醇浓度为20 - 29μg/dL)。维生素A缺乏的儿童身高(=0.09)和体重平均百分位数、淋巴细胞增殖反应及IL-2活性略低(>0.1),但C反应蛋白平均值(=0.05)、疼痛危象发作次数和炎症(=0.1)以及健康评分(>0.1)均高于非维生素A缺乏的儿童。淋巴细胞增殖反应与健康评分、疼痛危象发作次数及接受的血液单位呈负相关,但与视黄醇结合蛋白呈正相关(<0.05至=0.1)。
识别并纠正SCD患儿欠佳的维生素A状态可能会改善免疫力,并减轻与该疾病相关的某些健康并发症。