Department of Hematology, Children’s Hospital and Research Center Oakland, 5700 Martin Luther King Jr Way, Oakland, CA 94609, USA.
J Acad Nutr Diet. 2012 Jul;112(7):980-90. doi: 10.1016/j.jand.2012.01.017. Epub 2012 May 1.
Patients with thalassemia have low circulating levels of many nutrients, but the contribution of dietary intake has not been assessed.
Our objective was to assess dietary intake in a large contemporary sample of subjects with thalassemia.
A prospective, longitudinal cohort study using a validated food frequency questionnaire was conducted.
PARTICIPANTS/SETTING: Two hundred and twenty-one subjects (19.7±11.3 years, 106 were female) were categorized into the following age groups: young children (3 to 7.9 years), older children/adolescents (8 to 18.9 years), and adults (19 years or older); 78.8% had β-thalassemia and 90% were chronically transfused. This study took place at 10 hematology outpatient clinics in the United States and Canada.
We conducted a comparison of intake with US Dietary Reference Intakes and correlated dietary intake of vitamin D with serum 25-OH vitamin D and dietary iron with total body iron stores.
Intake was defined as inadequate if it was less than the estimated average requirement. χ(2), Fisher's exact, and Student's t test were used to compare intake between age categories and logistic regression analysis to test the relationship between intake and outcomes, controlling for age, sex, and race.
More than 30% of subjects consumed inadequate levels of vitamin A, D, E, K, folate, calcium, and magnesium. The only nutrients for which >90% of subjects consumed adequate amounts were riboflavin, vitamin B-12, and selenium. Dietary inadequacy increased with increasing age group (P<0.01) for vitamins A, C, E, B-6, folate, thiamin, calcium, magnesium, and zinc. More than half of the sample took additional supplements of calcium and vitamin D, although circulating levels of 25-OH vitamin D remained insufficient in 61% of subjects. Dietary iron intake was not related to total body iron stores.
Subjects with thalassemia have reduced intake of many key nutrients. These preliminary findings of dietary inadequacy are concerning and support the need for nutritional monitoring to determine which subjects are at greatest risk for nutritional deficiency. Future research should focus on the effect of dietary quality and nutritional status on health outcomes in thalassemia.
患有地中海贫血症的患者体内许多营养物质的循环水平较低,但饮食摄入的影响尚未得到评估。
我们的目的是评估大量当代地中海贫血症患者的饮食摄入情况。
使用经过验证的食物频率问卷进行了一项前瞻性、纵向队列研究。
参与者/设置:221 名患者(19.7±11.3 岁,106 名女性)分为以下年龄组:幼儿(3 至 7.9 岁)、大龄儿童/青少年(8 至 18.9 岁)和成年人(19 岁或以上);78.8%为β地中海贫血,90%为慢性输血者。本研究在美国和加拿大的 10 个血液科门诊进行。
我们比较了维生素 D 与血清 25-羟维生素 D 和膳食铁与总铁储存之间的摄入情况,并将维生素 D 的饮食摄入与血清 25-羟维生素 D 和膳食铁与总铁储存进行了相关性分析。
如果摄入量低于估计平均需求量,则定义为不足。使用 χ(2)、Fisher 确切检验和 Student's t 检验比较不同年龄组的摄入量,使用逻辑回归分析检验摄入量与结局之间的关系,同时控制年龄、性别和种族。
超过 30%的患者摄入的维生素 A、D、E、K、叶酸、钙和镁不足。只有超过 90%的患者摄入足够的核黄素、维生素 B-12 和硒。随着年龄组的增加(P<0.01),维生素 A、C、E、B-6、叶酸、硫胺素、钙、镁和锌的摄入量不足情况也随之增加。尽管 61%的患者循环 25-羟维生素 D 水平仍然不足,但仍有超过一半的患者额外补充钙和维生素 D。膳食铁的摄入量与总铁储存无关。
地中海贫血症患者的许多关键营养素摄入量较低。这些初步的饮食不足发现令人担忧,支持需要进行营养监测以确定哪些患者面临最大的营养缺乏风险。未来的研究应重点关注饮食质量和营养状况对地中海贫血症患者健康结果的影响。