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      Parasitological, serological and molecular diagnosis of acute and chronic Chagas disease: from field to laboratory

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          Abstract

          There is no consensus on the diagnostic algorithms for many scenarios of Trypanosoma cruzi infection, which hinders the establishment of governmental guidelines in endemic and non-endemic countries. In the acute phase, parasitological methods are currently employed, and standardised surrogate molecular tests are being introduced to provide higher sensitivity and less operator-dependence. In the chronic phase, IgG-based serological assays are currently used, but if a single assay does not reach the required accuracy, PAHO/WHO recommends at least two immunological tests with different technical principles. Specific algorithms are applied to diagnose congenital infection, screen blood and organ donors or conduct epidemiological surveys. Detecting Chagas disease reactivation in immunosuppressed individuals is an area of increasing interest. Due to its neglect, enhancing access to diagnosis of patients at risk of suffering T. cruzi infection should be a priority at national and regional levels.

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          Most cited references128

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          Detection of loop-mediated isothermal amplification reaction by turbidity derived from magnesium pyrophosphate formation.

          The loop-mediated isothermal amplification (LAMP) is a novel nucleic acid amplification method that uses only one type of enzyme. One of the characteristics of the LAMP method is its ability to synthesize extremely large amount of DNA. Accordingly, a large amount of by-product, pyrophosphate ion, is produced, yielding white precipitate of magnesium pyrophosphate in the reaction mixture. Judging the presence or absence of this white precipitate allows easy distinction of whether nucleic acid was amplified by the LAMP method. Since an increase in the turbidity of the reaction mixture according to the production of precipitate correlates with the amount of DNA synthesized, real-time monitoring of the LAMP reaction was achieved by real-time measurement of turbidity. Copyright 2001 Academic Press.
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            GRADE guidelines: 2. Framing the question and deciding on important outcomes.

            GRADE requires a clear specification of the relevant setting, population, intervention, and comparator. It also requires specification of all important outcomes--whether evidence from research studies is, or is not, available. For a particular management question, the population, intervention, and outcome should be sufficiently similar across studies that a similar magnitude of effect is plausible. Guideline developers should specify the relative importance of the outcomes before gathering the evidence and again when evidence summaries are complete. In considering the importance of a surrogate outcome, authors should rate the importance of the patient-important outcome for which the surrogate is a substitute and subsequently rate down the quality of evidence for indirectness of outcome. Copyright © 2011 Elsevier Inc. All rights reserved.
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              Chagas disease

              Chagas disease is an anthropozoonosis from the American continent that has spread from its original boundaries through migration. It is caused by the protozoan Trypanosoma cruzi, which was identified in the first decade of the 20th century. Once acute infection resolves, patients can develop chronic disease, which in up to 30-40% of cases is characterised by cardiomyopathy, arrhythmias, megaviscera, and, more rarely, polyneuropathy and stroke. Even after more than a century, many challenges remain unresolved, since epidemiological control and diagnostic, therapeutic, and prognostic methods must be improved. In particular, the efficacy and tolerability profile of therapeutic agents is far from ideal. Furthermore, the population affected is older and more complex (eg, immunosuppressed patients and patients with cancer). Nevertheless, in recent years, our knowledge of Chagas disease has expanded, and the international networking needed to change the course of this deadly disease during the 21st century has begun.
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                Author and article information

                Journal
                Mem Inst Oswaldo Cruz
                Mem Inst Oswaldo Cruz
                mioc
                Memórias do Instituto Oswaldo Cruz
                Instituto Oswaldo Cruz, Ministério da Saúde
                0074-0276
                1678-8060
                01 June 2022
                2022
                : 117
                : e200444
                Affiliations
                [1 ]Instituto de Investigaciones en Ingeniería Genética y Biología Molecular Dr Hector Torres, CONICET, Laboratorio de Biología Molecular de la Enfermedad de Chagas, Ciudad de Buenos Aires, Argentina
                [2 ]Barcelona Institute for Global Health, University of Barcelona, Hospital Clinic, Barcelona, Spain
                [3 ]Foundation for Innovative New Diagnostics, Geneva, Switzerland
                Author notes
                + Corresponding author: schijman@ 123456dna.uba.ar

                AGS drafted the first version of the review; AP and JAP contributed with updated information on molecular methods; SAL - serology; JAP - RDTs; SAL and AGS designed Figure and Tables. All coauthors revised the text to reach consensus on the final version of the manuscript.

                Author information
                http://orcid.org/0000-0001-9805-3415
                Article
                00207
                10.1590/0074-02760200444
                9164950
                35613155
                0aa28527-04fc-49e3-9e4f-44fffb45fcf0

                This is an open-access article distributed under the terms of the Creative Commons Attribution License

                History
                : 30 August 2020
                : 13 January 2021
                Page count
                Figures: 1, Tables: 3, References: 118
                Categories
                Review

                chagas disease,trypanosoma cruzi,diagnosis,polymerase chain reaction,loop mediated isothermal amplification

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