Literature DB >> 34327432

Does group A strep have any skin in the ARF game?

Gregory J Tyrrell1,2.   

Abstract

•The observation that indigenous populations of New Zealand have high rates of GAS skin infections as well as high rates of ARF suggest the two diseases are linked.•It is therefore important to screen skin infections for GAS in all populations but especially in individuals of Māori and Pacific Islander heritage in New Zealand and treat those that are positive.•Failure to adequately treat GAS skin infections could potentially lead more serious skin infection manifestations and possibly invasive disease as well as ARF in vulnerable groups such as the Māroi and Pacific Islanders.•More work needs to be done to show GAS skin infections can lead to ARF.
© 2021 The Author(s).

Entities:  

Year:  2021        PMID: 34327432      PMCID: PMC8315609          DOI: 10.1016/j.lanwpc.2021.100114

Source DB:  PubMed          Journal:  Lancet Reg Health West Pac        ISSN: 2666-6065


Group A streptococci (GAS) (Streptococcus pyogenes) are a cause of several diseases with the most common being pharyngitis and skin/soft tissue infections such as superficial pyoderma. While it is known that an important sequalae of GAS pharyngitis is acute rheumatic fever (ARF), whether GAS skin infections also lead to ARF is not completely clear [1]. It is known that ARF is the result of an autoimmune response directed against GAS antigens during streptococcal pharyngitis [1]. This autoimmune response, which typically occurs after pharyngitis has resolved, may cause damage to the mitral and/or aortic heart valves leading to a long-term disease known as rheumatic heart disease (RHD) [1]. ARF has been taught in medical schools for decades to be a disease which is a sequalae of acute GAS pharyngitis. However, evidence is beginning to suggest that there is also an association of ARF with GAS skin infections in some populations [1], [2], [3]. We know that the rates of ARF are disproportionately high in indigenous communities located in tropical and subtropical parts of the world [1]. This has been documented in groups such as the Aboriginal populations in Australia and the Māroi and Pacific Islander populations of New Zealand [1,4]. In New Zealand, ARF and RHD have been shown to be diseases principally affecting the Māori and Pacific Islander populations in contrast to other groups such Asian and Europeans [5]. It is these groups that are also severely economically disadvantaged with high rates of poverty and overcrowded housing, conditions known to predispose individuals to GAS skin infections and ARF [5]. The rates of ARF in Māroi children aged 5–14 years from 2000 to 2009 have been reported as high as 40.2/100 000 and in the Pacific Islander population as high as 81.2/100 000 [6]. These rates sharply contrast with the non-Māroi non-Pacific Islander population rate of 2.1/100 000. In 2011 the New Zealand government created the Rheumatic Fever Prevention Programme with the goal of reducing the incidence of ARF in this country [7]. This program had success early on through targeting the reduction of GAS pharyngitis in school aged children. However, after a period, ARF rates started to rise again suggesting treating only GAS infected sore throats may not be the complete answer. Proving a clear linkage of GAS skin infections as a cause of ARF has not been straightforward. In this study, Julie Bennett and colleagues collected data on over 377 000 skin swabs over a seven-year period in northern New Zealand for which a significant proportion were GAS positive (13%) [8]. These investigators found that the skin infections in children caused by GAS were predominately in the Māroi (9.7 per 1000 person years) and Pacific Islander populations (15.9 per 1000 person years) as opposed to other ethnicities (0.8 for Asian and 2.2 for European/other). The study went further and looked at rates of ARF over this same time. They found that ARF rates in Pacific Islanders under 20 years of age were 70 times higher than other ethnicities [8]. Interestingly, a parallel study analyzing the rates of GAS pharyngitis in the same population found similar GAS pharyngitis rates regardless of ethnicity [6]. This contrasts with the high rates of GAS skin disease identified in the Māroi and Pacific Islander populations and lower rates in other ethnic populations. High GAS skin infection positivity rates and high rates of ARF in the Pacific Islanders and Māori populations suggest GAS skin infections maybe drivers of ARF and, later in life, RHD in these populations. While studies suggest this to be the case, conclusively proving this though is no simple task. How does this work influence clinical practice? Based on the findings in the accompanying article as well as previous investigations, skin infections in New Zealand (especially in Pacific Islanders and Māori), need to be investigated for a causative bacterial agent and if GAS are present, be treated with antibiotics until the infection is resolved. The potential risk of ARF in these populations is too high not to investigate and if GAS is causing a skin infection, treat. Work to clinically resolve skin infections should receive the same attention as treating other infections, especially in regions where elevated rates of ARF have been documented. The findings from the accompanying article adds to the growing evidence that GAS skin infections likely contribute to high rates of ARF in disadvantage populations in New Zealand. Drawing a definitive link is not easy though and clearly more research needs to be done to conclusively tie the two diseases together. Important questions yet to be answered regarding GAS skin infections and ARF include: Does reducing the burden of GAS skin infections in populations such as Māroi and Pacific Islanders also reduce the prevalence of ARF and subsequent RHD? If GAS skin infections are the prevalent cause of ARF in New Zealand's indigenous populations, what is the immunological mechanism for this?

Declaration of Competing Interest

No conflict of interest.
  7 in total

1.  Primary prevention of rheumatic fever in the 21st century: evaluation of a national programme.

Authors:  Susan J Jack; Deborah A Williamson; Yvonne Galloway; Nevil Pierse; Jane Zhang; Jane Oliver; Richard J Milne; Graham Mackereth; Catherine M Jackson; Andrew C Steer; Jonathan R Carapetis; Michael G Baker
Journal:  Int J Epidemiol       Date:  2018-10-01       Impact factor: 7.196

Review 2.  Acute rheumatic fever and rheumatic heart disease.

Authors:  Jonathan R Carapetis; Andrea Beaton; Madeleine W Cunningham; Luiza Guilherme; Ganesan Karthikeyan; Bongani M Mayosi; Craig Sable; Andrew Steer; Nigel Wilson; Rosemary Wyber; Liesl Zühlke
Journal:  Nat Rev Dis Primers       Date:  2016-01-14       Impact factor: 52.329

Review 3.  Streptococcal skin infection and rheumatic heart disease.

Authors:  Tom Parks; Pierre R Smeesters; Andrew C Steer
Journal:  Curr Opin Infect Dis       Date:  2012-04       Impact factor: 4.915

Review 4.  Acute rheumatic fever: a chink in the chain that links the heart to the throat?

Authors:  Malcolm McDonald; Bart J Currie; Jonathan R Carapetis
Journal:  Lancet Infect Dis       Date:  2004-04       Impact factor: 25.071

5.  Distribution of Streptococcal Pharyngitis and Acute Rheumatic Fever, Auckland, New Zealand, 2010-2016.

Authors:  Jane Oliver; Arlo Upton; Susan J Jack; Nevil Pierse; Deborah A Williamson; Michael G Baker
Journal:  Emerg Infect Dis       Date:  2020-06       Impact factor: 6.883

6.  Rising Ethnic Inequalities in Acute Rheumatic Fever and Rheumatic Heart Disease, New Zealand, 2000-2018.

Authors:  Julie Bennett; Jane Zhang; William Leung; Susan Jack; Jane Oliver; Rachel Webb; Nigel Wilson; Dianne Sika-Paotonu; Matire Harwood; Michael G Baker
Journal:  Emerg Infect Dis       Date:  2021-01       Impact factor: 6.883

7.  Estimating the risk of acute rheumatic fever in New Zealand by age, ethnicity and deprivation.

Authors:  J K Gurney; J Stanley; M G Baker; N J Wilson; D Sarfati
Journal:  Epidemiol Infect       Date:  2016-06-17       Impact factor: 4.434

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.