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铁强化对加纳患有血红蛋白病和不同ABO血型的学龄前儿童贫血及疟疾风险的影响。

Effect of iron fortification on anaemia and risk of malaria among Ghanaian pre-school children with haemoglobinopathies and different ABO blood groups.

作者信息

Tchum Samuel Kofi, Sakyi Samuel Asamoah, Arthur Fareed, Adu Bright, Abubakar Latifatu Alhassan, Oppong Felix Boakye, Dzabeng Francis, Amoani Benjamin, Gyan Thomas, Asante Kwaku Poku

机构信息

Department of Biochemistry and Biotechnology, College of Sciences, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.

Kintampo Health Research Centre, Ghana Health Service, Kintampo-North, Bono East Region, Ghana.

出版信息

BMC Nutr. 2023 Mar 23;9(1):56. doi: 10.1186/s40795-023-00709-w.

Abstract

BACKGROUND

Haemoglobinopathies such as sickle cell disorder and glucose-6-phosphate dehydrogenase (G6PD) deficiency as well as differences in ABO blood groups have been shown to influence the risk of malaria and/or anaemia in malaria-endemic areas. This study assessed the effect of adding MNP containing iron to home-made weaning meals on anaemia and the risk of malaria in Ghanaian pre-school children with haemoglobinopathies and different ABO blood groups.

METHODS

This study was a double-blind, randomly clustered trial conducted within six months among infants and young children aged 6 to 35 months in rural Ghana (775 clusters, n = 860). Participants were randomly selected into clusters to receive daily semiliquid home-prepared meals mixed with either micronutrient powder without iron (noniron group) or with iron (iron group; 12.5 mg of iron daily) for 5 months. Malaria infection was detected by microscopy, blood haemoglobin (Hb) levels were measured with a HemoCue Hb analyzer, the reversed ABO blood grouping microtube assay was performed, and genotyping was performed by PCR-RFLP analysis.

RESULTS

The prevalence of G6PD deficiency among the study participants was 11.2%. However, the prevalence of G6PD deficiency in hemizygous males (8.5%) was significantly higher than that in homozygous females (2.7%) (p = 0.005). The prevalence rates of sickle cell traits (HbAS and HbSC) and sickle cell disorder (HbSS) were 17.5% and 0.5%, respectively. Blood group O was dominant (41.4%), followed by blood group A (29.6%) and blood group B (23.3%), while blood group AB (5.7%) had the least frequency among the study participants. We observed that children on an iron supplement with HbAS had significantly moderate anaemia at the endline (EL) compared to the baseline level (BL) (p = 0.004). However, subjects with HbAS and HbAC and blood groups A and O in the iron group had a significantly increased number of malaria episodes at EL than at BL (p < 0.05). Furthermore, children in the iron group with HbSS (p < 0.001) and the noniron group with HbCC (p = 0.010) were significantly less likely to develop malaria.

CONCLUSIONS

Iron supplementation increased anaemia in children with HbAS genotypes and provided less protection against malaria in children with HbAC and AS and blood groups A and O.

TRIAL REGISTRATION

clinicaltrials.gov Identifier: NCT01001871 . Registered 27/10/2009.

REGISTRATION NUMBER

https://clinicaltrials.gov/ct2/show/record/NCT01001871 .

摘要

背景

镰状细胞病和葡萄糖-6-磷酸脱氢酶(G6PD)缺乏症等血红蛋白病以及ABO血型差异已被证明会影响疟疾流行地区疟疾和/或贫血的风险。本研究评估了在加纳患有血红蛋白病和不同ABO血型的学龄前儿童的自制断奶餐中添加含铁多种微量营养素粉(MNP)对贫血和疟疾风险的影响。

方法

本研究是一项双盲随机整群试验,在加纳农村地区6至35个月的婴幼儿中进行,为期6个月(775个群组,n = 860)。参与者被随机分组,接受每日与不含铁的微量营养素粉(非铁组)或含铁(铁组;每日12.5毫克铁)混合的半流质家庭自制餐,持续5个月。通过显微镜检测疟疾感染,用HemoCue血红蛋白分析仪测量血血红蛋白(Hb)水平,进行反向ABO血型微管检测,并通过聚合酶链反应-限制性片段长度多态性分析(PCR-RFLP)进行基因分型。

结果

研究参与者中G6PD缺乏症的患病率为11.2%。然而,半合子男性中G6PD缺乏症的患病率(8.5%)显著高于纯合子女性(2.7%)(p = 0.005)。镰状细胞性状(HbAS和HbSC)和镰状细胞病(HbSS)的患病率分别为17.5%和0.5%。O血型占主导(41.4%),其次是A血型(29.6%)和B血型(23.3%),而AB血型(5.7%)在研究参与者中频率最低。我们观察到,与基线水平(BL)相比,接受铁补充剂的HbAS儿童在研究终点(EL)时中度贫血显著(p = 0.004)。然而,铁组中患有HbAS和HbAC以及A和O血型的受试者在EL时的疟疾发作次数比BL时显著增加(p < 0.05)。此外,铁组中患有HbSS的儿童(p < 0.001)和非铁组中患有HbCC的儿童(p = 0.010)患疟疾的可能性显著降低。

结论

铁补充剂增加了HbAS基因型儿童的贫血,并为患有HbAC、AS以及A和O血型的儿童提供了较少的疟疾防护。

试验注册

clinicaltrials.gov标识符:NCT01001871。2009年10月27日注册。

注册号

https://clinicaltrials.gov/ct2/show/record/NCT01001871

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26f4/10035121/891870a63cbc/40795_2023_709_Fig1_HTML.jpg

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