Literature DB >> 22551675

Inadequate dietary intake in patients with thalassemia.

Ellen B Fung1, Yan Xu, Felicia Trachtenberg, Isaac Odame, Janet L Kwiatkowski, Ellis J Neufeld, Alexis A Thompson, Jeanne Boudreaux, Charles T Quinn, Elliott P Vichinsky.   

Abstract

BACKGROUND: Patients with thalassemia have low circulating levels of many nutrients, but the contribution of dietary intake has not been assessed.
OBJECTIVE: Our objective was to assess dietary intake in a large contemporary sample of subjects with thalassemia.
DESIGN: 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. MAIN OUTCOME MEASURES: 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. STATISTICAL ANALYSES PERFORMED: 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.
RESULTS: 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.
CONCLUSIONS: 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.
Copyright © 2012 Academy of Nutrition and Dietetics. Published by Elsevier Inc. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22551675      PMCID: PMC3419338          DOI: 10.1016/j.jand.2012.01.017

Source DB:  PubMed          Journal:  J Acad Nutr Diet        ISSN: 2212-2672            Impact factor:   4.910


  37 in total

1.  Dietary reference intakes for energy, carbohydrate, fiber, fat, fatty acids, cholesterol, protein and amino acids.

Authors:  Paula Trumbo; Sandra Schlicker; Allison A Yates; Mary Poos
Journal:  J Am Diet Assoc       Date:  2002-11

2.  Oxidative stress and inflammation in iron-overloaded patients with beta-thalassaemia or sickle cell disease.

Authors:  Patrick B Walter; Ellen B Fung; David W Killilea; Qing Jiang; Mark Hudes; Jacqueline Madden; John Porter; Patricia Evans; Elliott Vichinsky; Paul Harmatz
Journal:  Br J Haematol       Date:  2006-10       Impact factor: 6.998

3.  Adequacy of dietary intake declines with age in children with sickle cell disease.

Authors:  Deborah A Kawchak; Joan I Schall; Babette S Zemel; Kwaku Ohene-Frempong; Virginia A Stallings
Journal:  J Am Diet Assoc       Date:  2007-05

4.  Changes in the epidemiology of thalassemia in North America: a new minority disease.

Authors:  Elliott P Vichinsky; Eric A MacKlin; John S Waye; Fred Lorey; Nancy F Olivieri
Journal:  Pediatrics       Date:  2005-11-15       Impact factor: 7.124

5.  Practice paper of the American Dietetic Association: using the Dietary Reference Intakes.

Authors:  Suzanne P Murphy; Susan I Barr
Journal:  J Am Diet Assoc       Date:  2011-05

6.  Study of serum zinc in relation to nutritional status among thalassemia patients in Damanhour Medical National Institute.

Authors:  Samia I Fikry; Saneya A Saleh; Nadia N Sarkis; Hoda Mangoud
Journal:  J Egypt Public Health Assoc       Date:  2003

Review 7.  Changing patterns of thalassemia worldwide.

Authors:  Elliott P Vichinsky
Journal:  Ann N Y Acad Sci       Date:  2005       Impact factor: 5.691

8.  Nutritional deficiencies in patients with thalassemia.

Authors:  Ellen B Fung
Journal:  Ann N Y Acad Sci       Date:  2010-08       Impact factor: 5.691

9.  Relative validity of the Iowa Fluoride Study targeted nutrient semi-quantitative questionnaire and the block kids' food questionnaire for estimating beverage, calcium, and vitamin D intakes by children.

Authors:  Teresa A Marshall; Julie M Eichenberger Gilmore; Barbara Broffitt; Phyllis J Stumbo; Steven M Levy
Journal:  J Am Diet Assoc       Date:  2008-03

10.  Iron metabolism in thalassemia and sickle cell disease.

Authors:  Raffaella Mariani; Paola Trombini; Matteo Pozzi; Alberto Piperno
Journal:  Mediterr J Hematol Infect Dis       Date:  2009-10-27       Impact factor: 2.576

View more
  7 in total

1.  Guidelines for the Standard Monitoring of Patients With Thalassemia: Report of the Thalassemia Longitudinal Cohort.

Authors:  Venée N Tubman; Ellen B Fung; Maria Vogiatzi; Alexis A Thompson; Zora R Rogers; Ellis J Neufeld; Janet L Kwiatkowski
Journal:  J Pediatr Hematol Oncol       Date:  2015-04       Impact factor: 1.289

2.  Zinc status affects glucose homeostasis and insulin secretion in patients with thalassemia.

Authors:  Ellen B Fung; Ginny Gildengorin; Siddhant Talwar; Leah Hagar; Ashutosh Lal
Journal:  Nutrients       Date:  2015-06-02       Impact factor: 5.717

3.  Final Height and Endocrine Complications in Patients with β-Thalassemia Intermedia: Our Experience in Non-Transfused Versus Infrequently Transfused Patients and Correlations with Liver Iron Content.

Authors:  Mohamed A Yassin; Ashraf T Soliman; Vincenzo De Sanctis; Khadra S Yassin; Mohammad Aj Abdulla
Journal:  Mediterr J Hematol Infect Dis       Date:  2019-05-01       Impact factor: 2.576

Review 4.  A contemporary therapeutic approach to bone disease in beta-thalassemia - a review.

Authors:  Dimitrios Stefanopoulos; Nikolaos A Papaioannou; Athanassios G Papavassiliou; George Mastorakos; Andromachi Vryonidou; Aikaterini Michou; Ismene A Dontas; George Lyritis; Eva Kassi; Symeon Tournis
Journal:  J Frailty Sarcopenia Falls       Date:  2018-03-01

5.  Evaluation of effective factors in the acceptance of mobile health technology using the unified theory of acceptance and use of technology (UTAUT), case study: Blood transfusion complications in thalassemia patients.

Authors:  Shirindokht Farhady; Mohammad Mehdi Sepehri; Ali Akbar Pourfathollah
Journal:  Med J Islam Repub Iran       Date:  2020-07-22

6.  Assessment of the Nutritional Status, Bone Mineralization, and Anthropometrics of Children with Thalassemia Major.

Authors:  Serap Cevher Bulgurcu; Aylin Canbolat Ayhan; Hamdi Cihan Emeksiz; Fahri Ovali
Journal:  Medeni Med J       Date:  2021-12-19

7.  Nutritional Status in a Sample of Patients With β-Thalassemia Major.

Authors:  Irene Lidoriki; George Stavrou; Dimitrios Schizas; Maximos Frountzas; Lampros Fotis; Alkistis Kapelouzou; Smaro Kokkota; Barbara Fyntanidou; Katerina Kotzampassi
Journal:  Cureus       Date:  2022-08-14
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.