Literature DB >> 26855061

Nutrient Insufficiencies/Deficiencies in Children With Sickle Cell Disease and Its Association With Increased Disease Severity.

David J Martyres1, Abi Vijenthira2, Nick Barrowman3, Sydney Harris-Janz4, Christine Chretien4, Robert J Klaassen4.   

Abstract

BACKGROUND: Sickle cell disease (SCD) is characteristically described as a disease of hemolytic anemia and vaso-occlusive crises (VOCs). However, patients suffer from a multitude of other problems including impaired development, chronic pain, and increased susceptibility to infection. Nutritional deficiency has been implicated as a contributor to these issues. PROCEDURE: We reported the nutrition status with respect to vitamin D, zinc, B6, B12, folate, and homocysteine serum levels in Canadian children with SCD (n = 91). We also tested for associations between nutrients and markers of disease severity and growth.
RESULTS: Almost half the sample (42%) had multiple nutrient insufficiencies/deficiencies, and a further 27% had a single insufficiency/deficiency. The most common insufficiency/deficiency was zinc in 57% followed by calcidiol (25 dihydroxyvitamin D (25(OH)D)) (52%). Sixteen percent of patients had low vitamin B6 levels, while folate, calcitriol (1,25(OH)D), and homocysteine levels were normal. Increased number of vitamin insufficiencies/deficiencies was associated with increasing disease severity (P = 0.018). Zinc insufficiency/deficiency was significantly associated with an increased number of home pain crises (P = 0.001) and an increased incidence of hospitalizations for VOCs (P = 0.01).
CONCLUSIONS: Our findings show that patients with SCD commonly have multiple nutrient insufficiencies/deficiencies and support the growing evidence for the link between low zinc and increased VOC. It also indicates that increased nutrient insufficiencies/deficiencies are associated with increased disease severity in SCD. Prospective studies with larger samples are needed to further elucidate the relationship between nutrient deficiencies and SCD, and to determine whether nutrient supplementation can improve the disease course.
© 2016 Wiley Periodicals, Inc.

Entities:  

Keywords:  nutrient deficiency; pain; sickle cell disease; vitamin d; zinc

Mesh:

Year:  2016        PMID: 26855061     DOI: 10.1002/pbc.25940

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  12 in total

1.  Trace elements in children suffering from sickle cell anemia: A case-control study.

Authors:  Joseph K Sungu; Olivier Mukuku; Augustin Mulangu Mutombo; Paul Mawaw; Michel N Aloni; Oscar N Luboya
Journal:  J Clin Lab Anal       Date:  2017-02-15       Impact factor: 2.352

2.  Food insecurity, housing instability, and dietary quality among children with sickle cell disease: Assessment from a single urban center.

Authors:  Cristina R Fernández; Maureen Licursi; Randi Wolf; Margaret T Lee; Nancy S Green
Journal:  Pediatr Blood Cancer       Date:  2021-11-22       Impact factor: 3.167

3.  Vitamin D supplementation and pain-related emergency department visits in children with sickle cell disease.

Authors:  Anna M Hood; Charles T Quinn; Christopher D King; Lisa M Shook; James L Peugh; Lori E Crosby
Journal:  Complement Ther Med       Date:  2020-02-15       Impact factor: 2.446

4.  Influence of Nutrition on Disease Severity and Health-related Quality of Life in Adults with Sickle Cell Disease: A Prospective Study.

Authors:  Sanaa Kamal; Moheyeldeen Mohamed Naghib; Jamaan Al Zahrani; Huda Hassan; Karim Moawad; Omar Arrahman
Journal:  Mediterr J Hematol Infect Dis       Date:  2021-01-01       Impact factor: 2.576

5.  Possible Risk Factors for Severe Anemia in Hospitalized Sickle Cell Patients at Muhimbili National Hospital, Tanzania: Protocol for a Cross-Sectional Study.

Authors:  Furahini Tluway; Florence Urio; Bruno Mmbando; Raphael Zozimus Sangeda; Abel Makubi; Julie Makani
Journal:  JMIR Res Protoc       Date:  2018-02-28

6.  Comparative study of sickle cell anemia and hemoglobin SC disease: clinical characterization, laboratory biomarkers and genetic profiles.

Authors:  Milena Magalhães Aleluia; Teresa Cristina Cardoso Fonseca; Regiana Quinto Souza; Fábia Idalina Neves; Caroline Conceição da Guarda; Rayra Pereira Santiago; Bruna Laís Almeida Cunha; Camylla Villas Boas Figueiredo; Sânzio Silva Santana; Silvana Sousa da Paz; Júnia Raquel Dutra Ferreira; Bruno Antônio Veloso Cerqueira; Marilda de Souza Gonçalves
Journal:  BMC Hematol       Date:  2017-09-15

7.  In Vitro Lymphocyte Functions in Undernourished Children With Sickle Cell Anemia.

Authors:  Solo R Kuvibidila; Renée Gardner; Maria C Velez; Lolie Yu; Rajasekharan P Warrier
Journal:  Ochsner J       Date:  2020

8.  Folic acid supplementation in children with sickle cell disease: study protocol for a double-blind randomized cross-over trial.

Authors:  Brock A Williams; Heather McCartney; Erin Adams; Angela M Devlin; Joel Singer; Suzanne Vercauteren; John K Wu; Crystal D Karakochuk
Journal:  Trials       Date:  2020-06-29       Impact factor: 2.279

Review 9.  Precipitating factors and targeted therapies in combating the perils of sickle cell disease--- A special nutritional consideration.

Authors:  Shahida A Khan; Ghazi Damanhouri; Ashraf Ali; Sarah A Khan; Aziz Khan; Ahmed Bakillah; Samy Marouf; Ghazi Al Harbi; Saeed H Halawani; Ahmad Makki
Journal:  Nutr Metab (Lond)       Date:  2016-08-08       Impact factor: 4.169

10.  Prevalence of Vitamin D Deficiency Varies Widely by Season in Canadian Children and Adolescents with Sickle Cell Disease.

Authors:  Kaitlyn L I Samson; Heather McCartney; Suzanne M Vercauteren; John K Wu; Crystal D Karakochuk
Journal:  J Clin Med       Date:  2018-01-30       Impact factor: 4.241

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