Department of Epidemiology and Public Health, Swiss Tropical and Public Health Institute, Basel, Switzerland.
Am J Clin Nutr. 2013 Jun;97(6):1364-74. doi: 10.3945/ajcn.112.050302. Epub 2013 Apr 24.
Iron deficiency (ID) is a major cause of anemia, along with other nutritional, parasitic, and genetic factors. Accurate biomarkers are needed to estimate the relative contribution of ID to anemia. Soluble transferrin receptor (sTfR) is thought to be unaffected by inflammation.
The objectives were to determine the difference in sTfR and plasma ferritin (PF) concentrations among infants (6-23 mo of age), school-age children (6-8 y of age), and women (15-25 y of age) with and without inflammation and with and without Plasmodium falciparum infection and to assess the effect of adjusting sTfR and PF for inflammation or for P. falciparum infection on the estimated prevalence of ID.
The data were derived from a 14-mo prospective longitudinal survey on anemia, which was conducted in the Taabo area, south-central Côte d'Ivoire.
At baseline, sTfR concentration was significantly higher in infants and school-age children with either inflammation or P. falciparum infection than in control individuals without inflammation or without P. falciparum infection. Individuals with inflammation had significantly higher PF concentrations than did subjects without inflammation. Adjustments in sTfR concentrations for inflammation or P. falciparum infection in infants and school-age children resulted in significantly lower ID prevalence. Adjustment of PF for inflammation and Plasmodium infection resulted in a higher ID prevalence in infants and women.
In Ivorian infants and school-age children, ID prevalence was considerably lower after adjustment of sTfR for inflammation. However, as the prevalence estimates for ID differed widely if based on sTfR or PF, caution is still needed when estimating ID prevalence in areas with a high prevalence of inflammation or malaria. This trial was registered at controlled-trials.com as ISRCTN02181959.
缺铁(ID)是贫血的主要原因之一,其他营养、寄生虫和遗传因素也是导致贫血的原因。需要准确的生物标志物来估计 ID 对贫血的相对贡献。可溶性转铁蛋白受体(sTfR)被认为不受炎症的影响。
本研究旨在确定伴有或不伴有炎症以及伴有或不伴有恶性疟原虫感染的婴儿(6-23 月龄)、学龄儿童(6-8 岁)和妇女(15-25 岁)之间 sTfR 和血浆铁蛋白(PF)浓度的差异,并评估调整 sTfR 和 PF 以消除炎症或恶性疟原虫感染对估计 ID 患病率的影响。
数据来自于科特迪瓦中南部 Taabo 地区一项为期 14 个月的前瞻性纵向贫血调查。
在基线时,伴有炎症或恶性疟原虫感染的婴儿和学龄儿童的 sTfR 浓度显著高于无炎症或无恶性疟原虫感染的对照组。伴有炎症的个体的 PF 浓度显著高于无炎症的个体。在婴儿和学龄儿童中,调整 sTfR 浓度以消除炎症或恶性疟原虫感染,导致 ID 的患病率显著降低。调整 PF 以消除炎症和恶性疟原虫感染,导致婴儿和妇女的 ID 患病率升高。
在科特迪瓦婴儿和学龄儿童中,调整 sTfR 以消除炎症后,ID 的患病率明显降低。然而,由于基于 sTfR 或 PF 的 ID 患病率估计值差异很大,因此在炎症或疟疾流行地区估计 ID 患病率时仍需谨慎。该试验在 controlled-trials.com 上注册为 ISRCTN02181959。