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      Global Burden of Leptospirosis: Estimated in Terms of Disability Adjusted Life Years

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          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Background

          Leptospirosis, a spirochaetal zoonosis, occurs in diverse epidemiological settings and affects vulnerable populations, such as rural subsistence farmers and urban slum dwellers. Although leptospirosis can cause life-threatening disease, there is no global burden of disease estimate in terms of Disability Adjusted Life Years (DALYs) available.

          Methodology/Principal Findings

          We utilised the results of a parallel publication that reported global estimates of morbidity and mortality due to leptospirosis. We estimated Years of Life Lost (YLLs) from age and gender stratified mortality rates. Years of Life with Disability (YLDs) were developed from a simple disease model indicating likely sequelae. DALYs were estimated from the sum of YLLs and YLDs. The study suggested that globally approximately 2·90 million DALYs are lost per annum (UIs 1·25–4·54 million) from the approximately annual 1·03 million cases reported previously. Males are predominantly affected with an estimated 2·33 million DALYs (UIs 0·98–3·69) or approximately 80% of the total burden. For comparison, this is over 70% of the global burden of cholera estimated by GBD 2010. Tropical regions of South and South-east Asia, Western Pacific, Central and South America, and Africa had the highest estimated leptospirosis disease burden.

          Conclusions/Significance

          Leptospirosis imparts a significant health burden worldwide, which approach or exceed those encountered for a number of other zoonotic and neglected tropical diseases. The study findings indicate that highest burden estimates occur in resource-poor tropical countries, which include regions of Africa where the burden of leptospirosis has been under-appreciated and possibly misallocated to other febrile illnesses such as malaria.

          Author Summary

          Leptospirosis is a zoonotic bacterial disease that affects vulnerable populations such as rural subsistence farmers and urban slum dwellers. Although leptospirosis can cause life-threatening clinical manifestations such as pulmonary hemorrhage syndrome and has a worldwide distribution, to date, the global burden of leptospirosis has not been estimated. The estimated 1.03 million cases annually result in a total of approximately 2.90 million Disability Adjusted Life Years. For comparison, this is over 70% of the global burden of cholera. Most of this burden of leptospirosis is the result of premature death and is suffered disproportionately by young adult males in resource-poor tropical countries. These estimates place leptospirosis as a leading cause of disease burden amongst zoonotic agents.

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          Most cited references17

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          Quantifying the burden of disease: the technical basis for disability-adjusted life years.

          C. Murray (1994)
          Detailed assumptions used in constructing a new indicator of the burden of disease, the disability-adjusted life year (DALY), are presented. Four key social choices in any indicator of the burden of disease are carefully reviewed. First, the advantages and disadvantages of various methods of calculating the duration of life lost due to a death at each age are discussed. DALYs use a standard expected-life lost based on model life-table West Level 26. Second, the value of time lived at different ages is captured in DALYs using an exponential function which reflects the dependence of the young and the elderly on adults. Third, the time lived with a disability is made comparable with the time lost due to premature mortality by defining six classes of disability severity. Assigned to each class is a severity weight between 0 and 1. Finally, a three percent discount rate is used in the calculation of DALYs. The formula for calculating DALYs based on these assumptions is provided.
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            Leptospira: the dawn of the molecular genetics era for an emerging zoonotic pathogen.

            Leptospirosis is a zoonotic disease that has emerged as an important cause of morbidity and mortality among impoverished populations. One hundred years after the discovery of the causative spirochaetal agent, little is understood about Leptospira spp. pathogenesis, which in turn has hampered the development of new intervention strategies to address this neglected disease. However, the recent availability of complete genome sequences for Leptospira spp. and the discovery of genetic tools for their transformation have led to important insights into the biology of these pathogens and their pathogenesis. We discuss the life cycle of the bacterium, the recent advances in our understanding and the implications for the future prevention of leptospirosis.
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              Leptospirosis: a zoonotic disease of global importance.

              In the past decade, leptospirosis has emerged as a globally important infectious disease. It occurs in urban environments of industrialised and developing countries, as well as in rural regions worldwide. Mortality remains significant, related both to delays in diagnosis due to lack of infrastructure and adequate clinical suspicion, and to other poorly understood reasons that may include inherent pathogenicity of some leptospiral strains or genetically determined host immunopathological responses. Pulmonary haemorrhage is recognised increasingly as a major, often lethal, manifestation of leptospirosis, the pathogenesis of which remains unclear. The completion of the genome sequence of Leptospira interrogans serovar lai, and other continuing leptospiral genome sequencing projects, promise to guide future work on the disease. Mainstays of treatment are still tetracyclines and beta-lactam/cephalosporins. No vaccine is available. Prevention is largely dependent on sanitation measures that may be difficult to implement, especially in developing countries.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS Negl Trop Dis
                PLoS Negl Trop Dis
                plos
                plosntds
                PLoS Neglected Tropical Diseases
                Public Library of Science (San Francisco, CA USA )
                1935-2727
                1935-2735
                2 October 2015
                October 2015
                : 9
                : 10
                : e0004122
                Affiliations
                [1 ]Section of Epidemiology, Vetsuisse Faculty, University of Zürich, Zürich, Switzerland
                [2 ]Fundação Oswaldo Cruz, Ministério da Saúde, Salvador, Bahia, Brazil
                [3 ]Department of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, Connecticut, United States of America
                [4 ]Institute of Collective Health, Federal University of Bahia (UFBA), Salvador, Brazil
                [5 ]Center for Analytical Sciences, Yale School of Public Health, New Haven, Connecticut, United States of America
                [6 ]WHO/FAO/OIE and National Leptospirosis Reference Center, Royal Tropical Institute, KIT Biomedical Research, Amsterdam, The Netherlands
                [7 ]Division of Information, Evidence, Research and Innovation (DIR), World Health Organization Regional Office for Europe, Copenhagen, Denmark
                [8 ]Department for the Control of Neglected Tropical Diseases, World Health Organization, Genève, Switzerland
                University of Tennessee, UNITED STATES
                Author notes

                The authors either served as members of the World Health Organization advisory body—the Leptospirosis Burden Epidemiology Reference Group or acted as advisors to LERG—without remuneration. The authors declare no other competing interests.

                Conceived and designed the experiments: PRT JEH FC JC MK MSMS MGAG CS AIK BAR. Performed the experiments: PRT JEH FC JC MK MSMS MGAG CS AIK BAR. Analyzed the data: PRT. Contributed reagents/materials/analysis tools: PRT JEH FC JC MK MSMS MGAG CS AIK BAR. Wrote the paper: PRT JEH FC JC MK MSMS MGAG CS AIK BAR.

                Article
                PNTD-D-15-01032
                10.1371/journal.pntd.0004122
                4591975
                26431366
                ed6b5c39-cfdf-4bfa-a37d-e03f59a4ad15
                Copyright @ 2015

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited

                History
                : 15 June 2015
                : 5 September 2015
                Page count
                Figures: 4, Tables: 5, Pages: 14
                Funding
                This work was supported by the World Health Organization, Brazilian Ministry of Education and National Institutes of Health (R01 AI052473, U01 AI088752, D43 TW00919, R25 TW009338, T32 AI007172, R24 TW007988). The World Health Organization approved the final manuscript before publication and thus their permission was required before the decision to publish. Two of the co-authors are also employees of the WHO. Thus the WHO did have an input into the the study design, analysis, preparation of the manuscript and decision to publish. Other funders played no role in these areas.
                Categories
                Research Article
                Custom metadata
                Data are within the manuscript, Supporting Information, or in associate manuscript "Global Morbidity and Mortality of Leptospirosis: A Systematic Review" by Costa et al http://journals.plos.org/plosntds/article?id=10.1371/journal.pntd.0003898.

                Infectious disease & Microbiology
                Infectious disease & Microbiology

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