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Proteinuria is associated with persistence of antibody to streptococcal M protein in Aboriginal Australians

Published online by Cambridge University Press:  01 February 1999

A. M. GOODFELLOW
Affiliation:
Menzies School of Health Research, PO Box 41096, Casuarina NT, Australia 0810
W. E. HOY
Affiliation:
Menzies School of Health Research, PO Box 41096, Casuarina NT, Australia 0810
K. S. SRIPRAKASH
Affiliation:
Menzies School of Health Research, PO Box 41096, Casuarina NT, Australia 0810
M. J. DALY
Affiliation:
Menzies School of Health Research, PO Box 41096, Casuarina NT, Australia 0810 Present address: Whitehead Institute for Biomedical Research, 9 Cambridge Centre, Cambridge, MA, 02142, USA.
M. P. REEVE
Affiliation:
Menzies School of Health Research, PO Box 41096, Casuarina NT, Australia 0810 Present address: Whitehead Institute for Biomedical Research, 9 Cambridge Centre, Cambridge, MA, 02142, USA.
J. D. MATHEWS
Affiliation:
Menzies School of Health Research, PO Box 41096, Casuarina NT, Australia 0810
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Abstract

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Aboriginal communities in Northern Australia with high rates of group A streptococcal (GAS) skin infection in childhood also have high rates of renal failure in adult life. In a cross-sectional study of one such high risk community, albuminuria was used as a marker of renal disease. The prevalence of albuminuria increased from 0/52 in subjects aged 10–19 years to 10/29 (32·9%) in those aged 50 or more (P<0·001). Antibodies to streptococcal M protein, markers of past GAS infection, were present in 48/52 (92%) at ages 10–19 years, 16/32 (50%) at ages 30–39, and 20/29 (69%) in those aged 50 or more. After allowing for the age-dependencies of albuminuria and of M protein antibodies (P<0·001) albuminuria was significantly associated with M protein antibodies (P<0·01). Thus, 72% of adults aged 30 or more with M protein antibodies also had albuminuria, compared with only 21% of those who were seronegative. More detailed modelling suggested that although most Aboriginal people in this community developed M protein antibodies following GAS infection in childhood, the development of proteinuria was associated with the persistence of such seropositivity into adult life. The models predicted that proteinuria developed at a mean age of 30 years in seropositive persons, at 45 years in seronegative persons who were overweight, and at 62 years in seronegative persons of normal weight. We demonstrated a clear association between evidence of childhood GAS infection and individual risk of proteinuria in adult life. This study provided a strong rationale for prevention of renal disease through the more effective control of GAS skin infections in childhood and through the prevention of obesity in adult life.

Type
Research Article
Copyright
© 1999 Cambridge University Press