Literature DB >> 30569002

Nutritional Deficiencies Are Common in Patients with Transfusion-Dependent Thalassemia and Associated with Iron Overload.

Elijah K Goldberg1, Sushrita Neogi1, Ashutosh Lal2, Annie Higa3, Ellen Fung1,2.   

Abstract

Patients with thalassemia are frequently deficient in key micronutrients. Attempts to correct these inadequacies through nutritional supplementation have been met with some success, although disparities between intake and circulating levels continue to be observed. This study employed a convenience sample of 41 well-nourished transfusion dependent patients with thalassemia to identify possible mechanisms behind nutritional deficiencies. Each subject completed a Block 2005© Food Frequency Questionnaire (FFQ), through which macro and micronutrient intake was quantified. Fasting blood was drawn to assess vitamins A, C, D, E, copper, selenium, zinc and hematologic parameters. Dietary intake was found to be inadequate compared to Institute of Medicine (IOM) recommendations for many of the fat-soluble vitamins, as well as calcium and zinc. Circulating deficiencies of vitamins C, D, copper, zinc and γ tocopherol were also present in over 20% of patients. Many individuals who consumed an adequate dietary intake had deficient levels of circulating nutrients, which suggest alternative etiologies of nutrient excretion or loss, in addition to higher micronutrient requirements. Liver iron concentration displayed a significant negative relationship with vitamins C (r=-0.62, p<0.001), E (r=-0.37, p=0.03), and zinc (r=-0.35, p=0.037), indicating that in iron-overloaded patients, these nutrients are either endogenously consumed at higher rates or sequestered within the liver, resulting in a functional nutrient deficiency. While this study identified hepatic iron overload to be a significant cause of nutritional deficits commonly observed in patients with thalassemia, multiple etiologies are simultaneously responsible. In response to these findings, nutritional status should be monitored regularly in at-risk patients with thalassemia, and prophylactically addressed with supplementation or aggressive chelation to avoid associated co-morbidities.

Entities:  

Keywords:  Food Frequency Questionnaire; iron overload; nutrition; thalassemia; vitamin C; vitamin D; zinc

Year:  2018        PMID: 30569002      PMCID: PMC6296481          DOI: 10.12691/jfnr-6-10-9

Source DB:  PubMed          Journal:  J Food Nutr Res (Newark)        ISSN: 2333-1119


  7 in total

1.  Nutrition in Thalassemia: A Systematic Review of Deficiency, Relations to Morbidity, and Supplementation Recommendations.

Authors:  Elijah K Goldberg; Ashutosh Lal; Ellen B Fung
Journal:  J Pediatr Hematol Oncol       Date:  2022-01-01       Impact factor: 1.289

Review 2.  Iron-Induced Hepatocarcinogenesis-Preventive Effects of Nutrients.

Authors:  Hiroyuki Tsuchiya
Journal:  Front Oncol       Date:  2022-06-27       Impact factor: 5.738

Review 3.  Vitamin and mineral supplementation for β-thalassemia during COVID-19 pandemic.

Authors:  Annette d'Arqom; Melvanda G Putri; Yovani Savitri; Andi Muh Rahul Alfaidin
Journal:  Future Sci OA       Date:  2020-08-18

4.  Moderate to severe liver siderosis and raised AST are independent risk factors for vitamin D insufficiency in β-thalassemia patients.

Authors:  Hadi Darvishi-Khezri; Hossein Karami; Mohammad Naderisorki; Mohammad Zahedi; Alireza Razavi; Mehrnoush Kosaryan; Aily Aliasgharian
Journal:  Sci Rep       Date:  2020-12-03       Impact factor: 4.379

5.  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

6.  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.  A Retrospective Long-Term Study on Age at Menarche and Menstrual Characteristics in 85 Young Women with Transfusion-Dependent β-Thalassemia (TDT).

Authors:  Salvatore Di Maio; Pierluigi Marzuillo; Demetris Mariannis; Soteroula Christou; Andreas Ellinides; Costantinos Christodoulides; Vincenzo de Sanctis
Journal:  Mediterr J Hematol Infect Dis       Date:  2021-07-01       Impact factor: 2.576

  7 in total

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