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Journal of the National Medical Association logoLink to Journal of the National Medical Association
. 2005 Dec;97(12):1622–1629.

Moderate chronic pain, weight and dietary intake in African-American adult patients with sickle cell disease.

Jennifer J Pells 1, Katherine E Presnell 1, Christopher L Edwards 1, Mary Wood 1, Myleme O Harrison 1, Laura DeCastro 1, Stephanie Johnson 1, Miriam Feliu 1, Stephanie Canada 1, Jude C Jonassaint 1, Camela Barker 1, Brittani Leach-Beale 1, Markece J Mathis 1, Katherine Applegate 1, Anita Holmes 1, Goldie Byrd 1, Elwood Robinson 1
PMCID: PMC2640739  PMID: 16396054

Abstract

In this exploratory study, we evaluated weight status and dietary intake patterns during painful episodes in adult patients with SCD. Specifically, we explored the relation between pain severity and body mass index (BMI), and we tested the hypothesis that dietary intake would be reduced and dietary content altered during periods of increased pain. We conducted an analysis of survey data from 62 patients involved in a longitudinal evaluation of the relationship of medical and psychosocial factors to pain. Nearly half of patients with SCD were overweight, and 20% were obese. BMI was positively related to interference associated with pain. Although BMI was not statistically associated with reported pain severity, >40% of patients reported that they perceived their pain to be affected by their weight. Less than 20% of patients reported that they perceived that their weight affected their pain. Regarding dietary patterns, the majority of patients reported eating less during episodes of pain and significantly decreasing their intake of fats and proteins. We conclude that there is a need to better understand the relation among weight, dietary patterns and pain in patients with SCD in order to provide patients with accurate education and effective treatment recommendations for managing their disease and reducing current and future risks of lifestyle and disease-related morbidities.

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Selected References

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  1. Abrams M. R., Phillips G., Jr, Whitworth E. Adaptation and coping: a look at a sickle cell patient population over age 30--an integral phase of the life long developmental process. J Health Soc Policy. 1994;5(3-4):141–160. doi: 10.1300/J045v05n03_09. [DOI] [PubMed] [Google Scholar]
  2. Calle E. E., Thun M. J., Petrelli J. M., Rodriguez C., Heath C. W., Jr Body-mass index and mortality in a prospective cohort of U.S. adults. N Engl J Med. 1999 Oct 7;341(15):1097–1105. doi: 10.1056/NEJM199910073411501. [DOI] [PubMed] [Google Scholar]
  3. Charache S., Terrin M. L., Moore R. D., Dover G. J., Barton F. B., Eckert S. V., McMahon R. P., Bonds D. R. Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia. Investigators of the Multicenter Study of Hydroxyurea in Sickle Cell Anemia. N Engl J Med. 1995 May 18;332(20):1317–1322. doi: 10.1056/NEJM199505183322001. [DOI] [PubMed] [Google Scholar]
  4. Edwards Christopher L., Scales Mischca T., Loughlin Charles, Bennett Gary G., Harris-Peterson Shani, De Castro Laura M., Whitworth Elaine, Abrams Mary, Feliu Miriam, Johnson Stephanie. A brief review of the pathophysiology, associated pain, and psychosocial issues in sickle cell disease. Int J Behav Med. 2005;12(3):171–179. doi: 10.1207/s15327558ijbm1203_6. [DOI] [PubMed] [Google Scholar]
  5. Harrison M. Ojinga, Edwards Christopher L., Koenig Harold G., Bosworth Hayden B., Decastro Laura, Wood Mary. Religiosity/spirituality and pain in patients with sickle cell disease. J Nerv Ment Dis. 2005 Apr;193(4):250–257. doi: 10.1097/01.nmd.0000158375.73779.50. [DOI] [PubMed] [Google Scholar]
  6. Hartz A. J., Fischer M. E., Bril G., Kelber S., Rupley D., Jr, Oken B., Rimm A. A. The association of obesity with joint pain and osteoarthritis in the HANES data. J Chronic Dis. 1986;39(4):311–319. doi: 10.1016/0021-9681(86)90053-6. [DOI] [PubMed] [Google Scholar]
  7. Inoue Koki, Zorrilla Eric P., Tabarin Antoine, Valdez Glenn R., Iwasaki Sinichi, Kiriike Nobuo, Koob George F. Reduction of anxiety after restricted feeding in the rat: implication for eating disorders. Biol Psychiatry. 2004 Jun 1;55(11):1075–1081. doi: 10.1016/j.biopsych.2004.01.026. [DOI] [PubMed] [Google Scholar]
  8. Kerns R. D., Turk D. C., Rudy T. E. The West Haven-Yale Multidimensional Pain Inventory (WHYMPI). Pain. 1985 Dec;23(4):345–356. doi: 10.1016/0304-3959(85)90004-1. [DOI] [PubMed] [Google Scholar]
  9. Lattimore Paul, Caswell Noreen. Differential effects of active and passive stress on food intake in restrained and unrestrained eaters. Appetite. 2004 Apr;42(2):167–173. doi: 10.1016/j.appet.2003.09.002. [DOI] [PubMed] [Google Scholar]
  10. Leikin S. L., Gallagher D., Kinney T. R., Sloane D., Klug P., Rida W. Mortality in children and adolescents with sickle cell disease. Cooperative Study of Sickle Cell Disease. Pediatrics. 1989 Sep;84(3):500–508. [PubMed] [Google Scholar]
  11. Marcus Dawn A. Obesity and the impact of chronic pain. Clin J Pain. 2004 May-Jun;20(3):186–191. doi: 10.1097/00002508-200405000-00009. [DOI] [PubMed] [Google Scholar]
  12. Platt O. S., Brambilla D. J., Rosse W. F., Milner P. F., Castro O., Steinberg M. H., Klug P. P. Mortality in sickle cell disease. Life expectancy and risk factors for early death. N Engl J Med. 1994 Jun 9;330(23):1639–1644. doi: 10.1056/NEJM199406093302303. [DOI] [PubMed] [Google Scholar]
  13. Power C., Frank J., Hertzman C., Schierhout G., Li L. Predictors of low back pain onset in a prospective British study. Am J Public Health. 2001 Oct;91(10):1671–1678. doi: 10.2105/ajph.91.10.1671. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Rees David C., Olujohungbe Ade D., Parker Norman E., Stephens Adrian D., Telfer Paul, Wright Josh, British Committee for Standards in Haematology General Haematology Task Force by the Sickle Cell Working Party Guidelines for the management of the acute painful crisis in sickle cell disease. Br J Haematol. 2003 Mar;120(5):744–752. doi: 10.1046/j.1365-2141.2003.04193.x. [DOI] [PubMed] [Google Scholar]
  15. Rodgers G. P. Overview of pathophysiology and rationale for treatment of sickle cell anemia. Semin Hematol. 1997 Jul;34(3 Suppl 3):2–7. [PubMed] [Google Scholar]
  16. Schlundt D. G., Taylor D., Hill J. O., Sbrocco T., Pope-Cordle J., Kasser T., Arnold D. A behavioral taxonomy of obese female participants in a weight-loss program. Am J Clin Nutr. 1991 May;53(5):1151–1158. doi: 10.1093/ajcn/53.5.1151. [DOI] [PubMed] [Google Scholar]
  17. Silva Célia Maria, Viana Marcos Borato. Growth deficits in children with sickle cell disease. Arch Med Res. 2002 May-Jun;33(3):308–312. doi: 10.1016/s0188-4409(01)00360-5. [DOI] [PubMed] [Google Scholar]
  18. Van Strien T., Rookus M. A., Bergers G. P., Frijters J. E., Defares P. B. Life events, emotional eating and change in body mass index. Int J Obes. 1986;10(1):29–35. [PubMed] [Google Scholar]
  19. Veith R., Galanello R., Papayannopoulou T., Stamatoyannopoulos G. Stimulation of F-cell production in patients with sickle-cell anemia treated with cytarabine or hydroxyurea. N Engl J Med. 1985 Dec 19;313(25):1571–1575. doi: 10.1056/NEJM198512193132503. [DOI] [PubMed] [Google Scholar]
  20. Wandel Margareta, Roos Gun. Work, food and physical activity. A qualitative study of coping strategies among men in three occupations. Appetite. 2005 Feb;44(1):93–102. doi: 10.1016/j.appet.2004.08.002. [DOI] [PubMed] [Google Scholar]
  21. Wison Schaeffer J. J., Gil K. M., Burchinal M., Kramer K. D., Nash K. B., Orringer E., Strayhorn D. Depression, disease severity, and sickle cell disease. J Behav Med. 1999 Apr;22(2):115–126. doi: 10.1023/a:1018755831101. [DOI] [PubMed] [Google Scholar]

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