Association of rheumatic fever with serum albumin concentration and body iron stores in Bangladeshi children: case-control studyBMJ 1998; 317 doi: https://doi.org/10.1136/bmj.317.7168.1287 (Published 07 November 1998) Cite this as: BMJ 1998;317:1287
- M Mostafa Zaman (), doctoral studenta,
- Nobuo Yoshiike, senior researcherb,
- Mian Abdur Rouf, microbiologistc,
- Sirajul Haque, professor of cardiologyc,
- Anisul Haque Chowdhury, research assistantc,
- Takeo Nakayama, assistant professora,
- Heizo Tanaka, professora
- a Department of Epidemiology, Medical Research Institute, Tokyo Medical and Dental University, 2-3-10 Kandasurugadai, Tokyo 101, Japan
- b Division of Adult Health Science, National Institute of Health and Nutrition, 1-23-1 Toyama, Tokyo 162
- c National Centre for Control of Rheumatic Fever and Heart Diseases, Sher-e-Bangla Nagar, Dhaka 1207, Bangladesh
- Correspondence to: Dr M M Zaman, National Centre for Control of Rheumatic Fever and Heart Diseases, Sher-e-Bangla Nagar, Dhaka 1207, Bangladesh
- Accepted 16 April 1998
Malnutrition in early life may cause metabolic1 and immune2 imbalance and consequently affect tissue reactivity of the child to group A β haemolytic streptococcal infection of the throat, leading to rheumatic fever.1 In developing countries protein and iron deficiencies during childhood are common and cause growth retardation,3 which is also found in rheumatic fever.4 Iron deficiency predisposes to repeated infections,3 which are necessary for a rheumatic attack. We examined whether rheumatic fever is associated with serum protein concentrations and body iron stores in Bangladeshi children.
Subjects, methods, and results
Recruitment of subjects and their socioeconomic background are described elsewhere.4 Briefly, 218 consecutive subjects aged 5 to 20 years who had a recent infection with group A β haemolytic streptococci were selected in the outpatient clinic of the National Centre for Control of Rheumatic Fever and Heart Diseases, Dhaka. Of them, 60 had rheumatic fever (as defined by the updated Jones criteria 1992) and 158 did not. Fasting convalescent blood samples (3-4 weeks after first contact) were obtained in 44 (73%) subjects with rheumatic fever and 139 (88%) without. Because the occurrence of rheumatic fever is strongly influenced by age and nutritional deprivation differs between sexes in Bangladesh, 44 subjects without rheumatic fever were randomly matched with cases for age (within one year) and sex.
Haemoglobin concentration and packed cell volume were measured in Bangladesh. Serum samples were stored at −80°C, transported to Tokyo on dry ice, and again stored at −80°C until used. Standard methods were used to determine nutritional markers. Transferrin saturation was calculated. Odds ratios and their 95% confidence intervals were obtained by univariate conditional logistic regression analyses (for matched subjects) for nutritional markers, which were entered into the model as continuous variables. Multiple logistic regression analyses were performed to calculate odds ratios adjusted for several socioeconomic factors that differed significantly between the groups. A measure of inflammation (C reactive protein concentration) was also considered as a covariate because it influences the nutritional markers of interest.
The mean (SD) age of the cases and controls was 12.6 (3.2) and 12.5 (3.2) years respectively, with 26 boys in each group. None of the cases had rheumatic heart disease or congestive heart failure. Three cases were presumed to have had an attack of rheumatic fever. The cases had lower serum albumin concentrations and all measures of body iron stores. Logistic regression analyses showed lower risk estimates for one unit increase in these variables (table). However, when confounding by socioeconomic factors and inflammation was taken into account, significance persisted for albumin concentration, packed cell volume, iron stores, and transferrin saturation. Analyses that excluded the three cases that were presumed to have had an attack of rheumatic fever gave similar results.
All subjects had recent infections with group A β haemolytic streptococci. The findings attributable to this particular inclusion criterion may widen our understanding of why most children with such infection escape a rheumatic attack while only a few do not. Our analyses adjusted for socioeconomic factors imply that low serum albumin concentrations and body iron stores may contribute to rheumatic fever. To rule out the possibility that differences in nutritional markers reflect differences in severity of inflammation, we adjusted for C reactive protein concentration in our analyses.
Iron deficiency might have favoured rheumatic fever by predisposing the cases to frequent infections with group A β haemolytic streptococci. The target organ lesions in patients with rheumatic fever predominantly contain T cells. We speculate that the tissue damage caused by T cell infiltration may be favoured by protein deprivation because T cell mediated immunological functions become exaggerated under mild to moderate chronic protein or protein energy deprivation.5 Although case-control studies have inherent limitations, our results suggest that deficiency of albumin and iron is linked to susceptibility to rheumatic fever.
The preliminary results of this work were presented at the 14th congress of rheumatology of the International League of Associations of Rheumatologists in Singapore, 8-13 June 1997. Fouzia Hasin, Amiruzzaman Khan, Billah Khan, and Mohammad Osman helped in recruiting the subjects. MMZ is a Monbusho (Japanese ministry of education, science, sports, and culture) scholar.
Contributors: MMZ initiated and coordinated the study, formulated study hypothesis, designed the protocol, discussed core ideas, analysed data, interpreted results, and wrote the manuscript. NY initiated the study, prepared the protocol, interpreted results, and revised the manuscript. MAR revised the laboratory aspect of the protocol, collected samples, and monitored the quality of diagnostic laboratory tests. SH revised the clinical aspect of the protocol, coordinated subject recruitment, and validated clinical diagnosis. AHC executed subject recruitment, data documentation, and quality control. TN helped in data analyses and revised critically the intellectual content of the manuscript. HT critically reviewed the protocol and manuscript and approved the final version for publication.
Funding This work was partially supported by a grant (4C-2) for international health cooperation research from the Ministry of Health and Welfare, Japan.
Conflict of interest None.