Kudirat A A, Shehu U A, Kolade E, Ibrahim M
Department of Pediatrics, Bayero University/Aminu Kano Teaching Hospital, Kano, Nigeria.
Department of Pediatrics, University of Ilorin/Teaching Hospital, Ilorin, Nigeria.
Niger J Clin Pract. 2019 Jan;22(1):16-23. doi: 10.4103/njcp.njcp_169_18.
Acute painful crisis due to vaso-occlusive event is the leading cause of hospitalization in patients with sickle cell anemia (SCA). Zinc deficiency in children with SCA is associated with increased frequency and severity of acute painful events. We determined serum zinc level in children with SCA during acute painful crisis and compared the same with children with SCA who are in steady state and healthy non-sickle cell disease children.
This was a descriptive longitudinal study, involving children with SCA age 6 months to 15 years at Aminu Kano Teaching Hospital, Kano, Northern Nigeria. Subjects were recruited into three groups, which consisted of SCA in acute painful crisis, SCA in steady state, and normal subjects with hemoglobin AA (HbAA). A total of 210 subjects were recruited, 70 subjects each for SCA in acute painful crisis, SCA in steady state, and HbAA groups, respectively. Serum zinc was analyzed with atomic absorption spectrophotometery. Serum zinc levels were repeated in children with SCA and acute painful crisis 4 weeks after resolution of painful events.
The mean serum zinc level of SCA with acute painful crisis was higher than SCA in steady state, but the difference was not statistically significant (24.4 [11.0] and 23.4 [7.4]) μg/dL, respectively (t = 16.04, P = 0.54). While the HbAA control had significantly higher mean serum zinc level than SCA groups, both in acute painful and in steady state (F = 59.3, P = 0.001). Among children with SCA and acute painful crisis, repeat serum zinc level 4 weeks after resolution of acute painful events was significantly higher than during pain crisis (t = 64, P = 0.001).
Zinc deficiency occurs in children with SCA and the deficiency is worsened by acute painful events Therefore, it is recommended that zinc level should be assessed and any deficiency treated. Supplementation of zinc should also be enhanced as this may reduce painful crisis in SCA.
血管闭塞事件引发的急性疼痛危象是镰状细胞贫血(SCA)患者住院的主要原因。SCA患儿的锌缺乏与急性疼痛事件的频率增加和严重程度相关。我们测定了SCA患儿急性疼痛危象期间的血清锌水平,并将其与处于稳定状态的SCA患儿以及健康的非镰状细胞病患儿进行比较。
这是一项描述性纵向研究,涉及尼日利亚北部卡诺市阿明努·卡诺教学医院6个月至15岁的SCA患儿。研究对象被分为三组,分别为处于急性疼痛危象的SCA患儿、处于稳定状态的SCA患儿以及血红蛋白为AA(HbAA)的正常受试者。共招募了210名受试者,急性疼痛危象的SCA患儿、稳定状态的SCA患儿和HbAA组各70名。采用原子吸收分光光度法分析血清锌。急性疼痛事件缓解4周后,对患有SCA和急性疼痛危象的患儿再次检测血清锌水平。
处于急性疼痛危象的SCA患儿的平均血清锌水平高于处于稳定状态的SCA患儿,但差异无统计学意义(分别为24.4[11.0]和23.4[7.4])μg/dL(t = 16.04,P = 0.54)。HbAA对照组的平均血清锌水平在急性疼痛和稳定状态下均显著高于SCA组(F = 59.3,P = 0.001)。在患有SCA和急性疼痛危象的患儿中,急性疼痛事件缓解4周后的血清锌水平显著高于疼痛危象期间(t = 64,P = 0.001)。
SCA患儿存在锌缺乏,且急性疼痛事件会使这种缺乏情况恶化。因此,建议评估锌水平并治疗任何缺乏情况。还应加强锌的补充,因为这可能减少SCA患儿的疼痛危象。