関: Chagas disease、Chagas' disease

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of or relating to the United States of America or its people or language or culture; "American citizens"; "American English"; "the American dream"
a native or inhabitant of a North American or Central American or South American country
a native or inhabitant of the United States
of or relating to or characteristic of the continents and islands of the Americas; "the American hemisphere"; "American flora and fauna"
North America and South America and Central America

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『アメリカ合衆国の』,米国の;アメリカ人の / 北アメリカの;北米人の / 南アメリカの;南米人の / 南北アメリカの;南北アメリカ人の / 米国人,アメリカ人 / 北(南)アメリカ人 / =American English
『アメリカ合衆国』,米国,アメリカ(《略》『Am.,Amer.』) / 《the Americas》南北アメリカ[イタリアの航海者･探検家Amerigo Vespucciの名前に由来]

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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2015/07/17 11:11:45」(JST)

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Chagas disease /ˈtʃɑːɡəs/, or American trypanosomiasis, is a tropical parasitic disease caused by the protozoan Trypanosoma cruzi.^[1] It is spread mostly by insects known as triatominae or kissing bugs.^[1] The symptoms change over the course of the infection. In the early stage, symptoms are typically either not present or mild and may include fever, swollen lymph nodes, headaches, or local swelling at the site of the bite.^[1] After 8–12 weeks, individuals enter the chronic phase of disease and in 60–70% it never produces further symptoms.^[2]^[3] The other 30 to 40% of people develop further symptoms 10 to 30 years after the initial infection,^[3] including enlargement of the ventricles of the heart in 20 to 30%, leading to heart failure.^[1] An enlarged esophagus or an enlarged colon may also occur in 10% of people.^[1]

T. cruzi is commonly spread to humans and other mammals by the blood-sucking "kissing bugs" of the subfamily Triatominae.^[4] These insects are known by a number of local names, including: vinchuca in Argentina, Bolivia, Chile and Paraguay, barbeiro (the barber) in Brazil, pito in Colombia, chinche in Central America, and chipo in Venezuela.^[5] The disease may also be spread through blood transfusion, organ transplantation, eating food contaminated with the parasites, and by vertical transmission (from a mother to her fetus).^[1] Diagnosis of early disease is by finding the parasite in the blood using a microscope.^[3] Chronic disease is diagnosed by finding antibodies for T. cruzi in the blood.^[3]

Prevention mostly involves eliminating kissing bugs and avoiding their bites.^[1] Other preventative efforts include screening blood used for transfusions.^[1] A vaccine has not been developed as of 2013.^[1] Early infections are treatable with the medication benznidazole or nifurtimox.^[1] Medication nearly always results in a cure if given early, but becomes less effective the longer a person has had Chagas disease.^[1] When used in chronic disease, medication may delay or prevent the development of end–stage symptoms.^[1] Benznidazole and nifurtimox cause temporary side effects in up to 40% of people^[1] including skin disorders, brain toxicity, and digestive system irritation.^[2]^[6]^[7]

It is estimated that 7 to 8 million people, mostly in Mexico, Central America and South America, have Chagas disease as of 2013.^[1] In 2006, Chagas was estimated to result in 12,500 deaths per year.^[2] Most people with the disease are poor,^[2] and most people with the disease do not realize they are infected.^[8] Large-scale population movements have increased the areas where Chagas disease is found and these include many European countries and the United States.^[1] These areas have also seen an increase in the years up to 2014.^[9] The disease was first described in 1909 by Carlos Chagas after whom it is named.^[1] It affects more than 150 other animals.^[2]

Signs and symptoms

An acute Chagas disease infection with swelling of the right eye (Romaña's sign).

Large scale anatomy of a heart that has been damaged by chronic Chagas disease – see also: Chagas heart, radiology

The human disease occurs in two stages: an acute stage, which occurs shortly after an initial infection, and a chronic stage that develops over many years.

The acute phase lasts for the first few weeks or months of infection. It usually occurs unnoticed because it is symptom-free or exhibits only mild symptoms that are not unique to Chagas disease. These can include fever, fatigue, body aches, muscle pain, headache, rash, loss of appetite, diarrhea, nausea, and vomiting. The signs on physical examination can include mild enlargement of the liver or spleen, swollen glands, and local swelling (a chagoma) where the parasite entered the body.^[10]

The most recognized marker of acute Chagas disease is called Romaña's sign, which includes swelling of the eyelids on the side of the face near the bite wound or where the bug feces were deposited or accidentally rubbed into the eye. Rarely, young children, or adults may die from the acute disease due to severe inflammation/infection of the heart muscle (myocarditis) or brain (meningoencephalitis).^[10] The acute phase also can be severe in people with weakened immune systems.^[4]

If symptoms develop during the acute phase, they usually resolve spontaneously within three to eight weeks in approximately 90% of individuals.^[2]^[6] Although the symptoms resolve, even with treatment the infection persists and enters a chronic phase. Of individuals with chronic Chagas disease, 60–80% will never develop symptoms (called indeterminate chronic Chagas disease), while the remaining 20–40% will develop life-threatening heart and/or digestive disorders during their lifetime (called determinate chronic Chagas disease). In 10% of individuals, the disease progresses directly from the acute form to a symptomatic clinical form of chronic Chagas disease.^[2]^[6]

The symptomatic (determinate) chronic stage affects the nervous system, digestive system and heart. About two-thirds of people with chronic symptoms have cardiac damage, including dilated cardiomyopathy, which causes heart rhythm abnormalities and may result in sudden death. About one-third of patients go on to develop digestive system damage, resulting in dilation of the digestive tract (megacolon and megaesophagus), accompanied by severe weight loss. Swallowing difficulties (secondary achalasia) may be the first symptom of digestive disturbances and may lead to malnutrition.^[11]

20% to 50% of individuals with intestinal involvement also exhibit cardiac involvement.^[11] Up to 10% of chronically infected individuals develop neuritis that results in altered tendon reflexes and sensory impairment. Isolated cases exhibit central nervous system involvement, including dementia, confusion, chronic encephalopathy and sensory and motor deficits.^[12]

The clinical manifestations of Chagas disease are due to cell death in the target tissues that occurs during the infective cycle, by sequentially inducing an inflammatory response, cellular lesions, and fibrosis. For example, intracellular amastigotes destroy the intramural neurons of the autonomic nervous system in the intestine and heart, leading to megaintestine and heart aneurysms, respectively. If left untreated, Chagas disease can be fatal, in most cases due to heart muscle damage.^[11]

Transmission

Rhodnius prolixus is the principal vector in Colombia, Venezuela, Guatemala, Honduras, and some parts of Nicaragua and El Salvador.

In Chagas-endemic areas, the main mode of transmission is through an insect vector called a triatomine bug.^[4] A triatomine becomes infected with T. cruzi by feeding on the blood of an infected person or animal. During the day, triatomines hide in crevices in the walls and roofs.^[4]

The bugs emerge at night, when the inhabitants are sleeping. Because they tend to feed on people's faces, triatomine bugs are also known as "kissing bugs". After they bite and ingest blood, they defecate on the person. Triatomines pass T. cruzi parasites (called trypomastigotes) in feces left near the site of the bite wound.^[4]

Scratching the site of the bite causes the trypomastigotes to enter the host through the wound, or through intact mucous membranes, such as the conjunctiva. Once inside the host, the trypomastigotes invade cells, where they differentiate into intracellular amastigotes. The amastigotes multiply by binary fission and differentiate into trypomastigotes, which are then released into the bloodstream. This cycle is repeated in each newly infected cell. Replication resumes only when the parasites enter another cell or are ingested by another vector.^[4] (See also: Life cycle and transmission of T. cruzi)

Dense vegetation (such as that of tropical rainforests) and urban habitats are not ideal for the establishment of the human transmission cycle. However, in regions where the sylvatic habitat and its fauna are thinned by economic exploitation and human habitation, such as in newly deforested areas, piassava palm culture areas, and some parts of the Amazon region, a human transmission cycle may develop as the insects search for new food sources.^[13]

T. cruzi can also be transmitted through blood transfusions. With the exception of blood derivatives (such as fractionated antibodies), all blood components are infective. The parasite remains viable at 4 °C for at least 18 days or up to 250 days when kept at room temperature. It is unclear whether T. cruzi can be transmitted through frozen-thawed blood components.^[14]

Other modes of transmission include organ transplantation, through breast milk,^[15] and by accidental laboratory exposure. Chagas disease can also be spread congenitally (from a pregnant woman to her baby) through the placenta, and accounts for approximately 13% of stillborn deaths in parts of Brazil.^[16]

Oral transmission is an unusual route of infection, but has been described. In 1991, farm workers in the state of Paraíba, Brazil, were infected by eating contaminated food; transmission has also occurred via contaminated açaí palm fruit juice and garapa.^[17]^[18]^[19]^[20]^[21] A 2007 outbreak in 103 Venezuelan school children was attributed to contaminated guava juice.^[22]

Chagas disease is a growing problem in Europe, because the majority of cases with chronic infection are asymptomatic and because of migration from Latin America.^[23]

Diagnosis

The presence of T. cruzi is diagnostic of Chagas disease. It can be detected by microscopic examination of fresh anticoagulated blood, or its buffy coat, for motile parasites; or by preparation of thin and thick blood smears stained with Giemsa, for direct visualization of parasites. Microscopically, T. cruzi can be confused with Trypanosoma rangeli, which is not known to be pathogenic in humans. Isolation of T. cruzi can occur by inoculation into mice, by culture in specialized media (for example, NNN, LIT); and by xenodiagnosis,^[24] where uninfected Reduviidae bugs are fed on the patient's blood, and their gut contents examined for parasites.^[11]

Various immunoassays for T. cruzi are available and can be used to distinguish among strains (zymodemes of T.cruzi with divergent pathogenicities). These tests include: detecting complement fixation, indirect hemagglutination, indirect fluorescence assays, radioimmunoassays, and ELISA. Alternatively, diagnosis and strain identification can be made using polymerase chain reaction (PCR).^[11]

Prevention

Awareness and prevention campaign poster in Cayenne, French Guiana, 2008

There is currently no vaccine against Chagas disease.^[25] Prevention is generally focused on decreasing the numbers of the insect that spreads it (Triatoma) and decreasing their contact with humans. This is done by using sprays and paints containing insecticides (synthetic pyrethroids), and improving housing and sanitary conditions in rural areas.^[26] For urban dwellers, spending vacations and camping out in the wilderness or sleeping at hostels or mud houses in endemic areas can be dangerous; a mosquito net is recommended. Some measures of vector control include:

A yeast trap can be used for monitoring infestations of certain species of triatomine bugs (Triatoma sordida, Triatoma brasiliensis, Triatoma pseudomaculata, and Panstrongylus megistus).^[27]
Promising results were gained with the treatment of vector habitats with the fungus Beauveria bassiana.^[28]
Targeting the symbionts of Triatominae through paratransgenesis can be done.^[29]

A number of potential vaccines are currently being tested. Vaccination with Trypanosoma rangeli has produced positive results in animal models.^[30] More recently, the potential of DNA vaccines for immunotherapy of acute and chronic Chagas disease is being tested by several research groups.^[31]

Blood transfusion was formerly the second-most common mode of transmission for Chagas disease, but the development and implementation of blood bank screening tests has dramatically reduced this risk in the 21st century. Blood donations in all endemic Latin American countries undergo Chagas screening, and testing is expanding in countries, such as France, Spain and the United States, that have significant or growing populations of immigrants from endemic areas.^[32]^[33] In Spain, donors are evaluated with a questionnaire to identify individuals at risk of Chagas exposure for screening tests.^[33]

The US FDA has approved two Chagas tests, including one approved in April 2010, and has published guidelines that recommend testing of all donated blood and tissue products.^[33]^[34] While these tests are not required in US, an estimated 75–90% of the blood supply is currently tested for Chagas, including all units collected by the American Red Cross, which accounts for 40% of the U.S. blood supply.^[34]^[35] The Chagas Biovigilance Network reports current incidents of Chagas-positive blood products in the United States, as reported by labs using the screening test approved by the FDA in 2007.^[36]

Management

There are two approaches to treating Chagas disease: antiparasitic treatment, to kill the parasite; and symptomatic treatment, to manage the symptoms and signs of the infection. Management uniquely involves addressing selective incremental failure of the parasympathetic nervous system. Autonomic disease imparted by Chagas may eventually result in megaesophagus, megacolon and accelerated dilated cardiomyopathy. The mechanisms that explain why Chagas targets the parasympathetic autonomic nervous system and spares the sympathetic autonomic nervous system remain poorly understood.

Medication

Antiparasitic treatment is most effective early in the course of infection, but is not limited to cases in the acute phase. Drugs of choice include azole or nitro derivatives, such as benznidazole^[37] or nifurtimox. Both agents are limited in their capacity to effect parasitologic cure (a complete elimination of T. cruzi from the body), especially in chronically infected patients, and resistance to these drugs has been reported.^[38]

Studies suggest antiparasitic treatment leads to parasitological cure in about 60–85% of adults and more than 90% of infants treated in the first year of acute phase Chagas disease. Children (aged six to 12 years) with chronic disease have a cure rate of about 60% with benznidazole. While the rate of cure declines the longer an adult has been infected with Chagas, treatment with benznidazole has been shown to slow the onset of heart disease in adults with chronic Chagas infections.^[2]^[11]

Treatment of chronic infection in women prior to or during pregnancy does not appear to reduce the probability the disease will be passed on to the infant. Likewise, it is unclear whether prophylactic treatment of chronic infection is beneficial in persons who will undergo immunosuppression (for example, organ transplant recipients) or in persons who are already immunosuppressed (for example, those with HIV infection).^[11]

Complications

In the chronic stage, treatment involves managing the clinical manifestations of the disease. For example, pacemakers and medications for irregular heartbeats, such as the anti-arrhythmia drug amiodarone, may be life saving for some patients with chronic cardiac disease,^[39] while surgery may be required for megaintestine. The disease cannot be cured in this phase, however. Chronic heart disease caused by Chagas disease is now a common reason for heart transplantation surgery. Until recently, however, Chagas disease was considered a contraindication for the procedure, since the heart damage could recur as the parasite was expected to seize the opportunity provided by the immunosuppression that follows surgery.^[40]

It was noted that survival rates in Chagas patients could be significantly improved by using lower dosages of the immunosuppressant drug cyclosporin. Recently, direct stem cell therapy of the heart muscle using bone marrow cell transplantation has been shown to dramatically reduce risks of heart failure in Chagas patients.^[41]

Epidemiology

Chagas disease in Latin America (endemic zones).

Chagas disease affects 8 to 10 million people living in endemic Latin American countries, with an additional 300,000–400,000 living in nonendemic countries, including Spain and the United States. An estimated 41,200 new cases occur annually in endemic countries, and 14,400 infants are born with congenital Chagas disease annually.^[2]^[11] in 2010 it resulted in approximately 10,300 deaths up from 9,300 in 1990.^[42]

The disease is present in 18 countries on the American continents, ranging from the southern United States to northern Argentina.^[4] Chagas exists in two different ecological zones. In the Southern Cone region, the main vector lives in and around human homes. In Central America and Mexico, the main vector species lives both inside dwellings and in uninhabited areas. In both zones, Chagas occurs almost exclusively in rural areas, where triatomines breed and feed on the more than 150 species from 24 families of domestic and wild mammals, as well as humans, that are the natural reservoirs of T. cruzi.^[43]

Although Triatominae bugs feed on them, birds appear to be immune to infection and therefore are not considered to be a T. cruzi reservoir. Even when colonies of insects are eradicated from a house and surrounding domestic animal shelters, they can re-emerge from plants or animals that are part of the ancient, sylvatic (referring to wild animals) infection cycle. This is especially likely in zones with mixed open savannah, with clumps of trees interspersed by human habitation.^[44]

The primary wildlife reservoirs for Trypanosoma cruzi in the United States include opossums, raccoons, armadillos, squirrels, woodrats, and mice.^[45] Opossums are particularly important as reservoirs, because the parasite can complete its life cycle in the anal glands of this animal without having to re-enter the insect vector.^[45] Recorded prevalence of the disease in opossums in the U.S. ranges from 8.3%^[45] to 37.5%.^[46]

Studies on raccoons in the Southeast have yielded infection rates ranging from 47%^[47] to as low as 15.5%.^[45] Armadillo prevalence studies have been described in Louisiana, and range from a low of 1.1%^[46] to 28.8%.^[48] Additionally, small rodents, including squirrels, mice, and rats, are important in the sylvatic transmission cycle because of their importance as bloodmeal sources for the insect vectors. A Texas study revealed 17.3% percent T. cruzi prevalence in 75 specimens representing four separate small rodent species.^[49]

Chronic Chagas disease remains a major health problem in many Latin American countries, despite the effectiveness of hygienic and preventive measures, such as eliminating the transmitting insects. However, several landmarks have been achieved in the fight against it in Latin America, including a reduction by 72% of the incidence of human infection in children and young adults in the countries of the Southern Cone Initiative, and at least three countries (Uruguay, in 1997, and Chile, in 1999, and Brazil in 2006) have been certified free of vectorial and transfusional transmission.^[11]^[50]^[51] In Argentina, vectorial transmission has been interrupted in 13 of the 19 endemic provinces,^[50] and major progress toward this goal has also been made in both Paraguay and Bolivia.

Screening of donated blood, blood components, and solid organ donors, as well as donors of cells, tissues, and cell and tissue products for T. cruzi is mandated in all Chagas-endemic countries and has been implemented.^[52] Approximately 300,000 infected people live in the United States, which is likely the result of immigration from Latin American countries.^[53] With increased population movements, the possibility of transmission by blood transfusion became more substantial in the United States. Transfusion blood and tissue products are now actively screened in the U.S., thus addressing and minimizing this risk.^[54]

History

Carlos Chagas, in his laboratory at the Instituto Oswaldo Cruz.

The disease was named after the Brazilian physician and epidemiologist Carlos Chagas, who first described it in 1909.^[55]^[56]^[57]^[58] The disease was not seen as a major public health problem in humans until the 1960s (the outbreak of Chagas disease in Brazil in the 1920s went widely ignored^[59]). Dr Chagas discovered that the intestines of Triatomidae (now Reduviidae: Triatominae) harbored a flagellate protozoan, a new species of the Trypanosoma genus, and was able to prove experimentally that it could be transmitted to marmoset monkeys that were bitten by the infected bug. Later studies showed squirrel monkeys were also vulnerable to infection.^[60]

Chagas named the pathogenic parasite as Trypanosoma cruzi^[55] and later that year as Schizotrypanum cruzi,^[57] both honoring Oswaldo Cruz, the noted Brazilian physician and epidemiologist who successfully fought epidemics of yellow fever, smallpox, and bubonic plague in Rio de Janeiro and other cities in the beginning of the 20th century. Chagas was also the first to unknowingly discover and illustrate the parasitic fungal genus Pneumocystis, later infamously linked to PCP (Pneumocystis pneumonia in AIDS victims).^[56] Confusion between the two pathogens' life-cycles led him to briefly recognize his genus Schizotrypanum, but following the description of Pneumocystis by others as an independent genus, Chagas returned to the use of the name Trypanosoma cruzi.

In Argentina, the disease is known as mal de Chagas-Mazza, in honor of Salvador Mazza, the Argentine physician who in 1926 began investigating the disease and over the years became the principal researcher of this disease in the country.^[61] Mazza produced the first scientific confirmation of the existence of Trypanosoma cruzi in Argentina in 1927, eventually leading to support from local and European medical schools and Argentine government policy makers.^[62]

It has been hypothesized that Charles Darwin might have suffered from Chagas disease as a result of a bite of the so-called great black bug of the Pampas (vinchuca) (see Charles Darwin's illness). The episode was reported by Darwin in his diaries of the Voyage of the Beagle as occurring in March 1835 to the east of the Andes near Mendoza. Darwin was young and generally in good health, though six months previously he had been ill for a month near Valparaiso, but in 1837, almost a year after he returned to England, he began to suffer intermittently from a strange group of symptoms, becoming incapacitated for much of the rest of his life. Attempts to test Darwin's remains at Westminster Abbey by using modern PCR techniques were met with a refusal by the Abbey's curator.^[63]

Research

Several experimental treatments have shown promise in animal models. These include inhibitors of oxidosqualene cyclase and squalene synthase,^[64]^[65] cysteine protease inhibitors,^[64]^[66] dermaseptins collected from frogs in the genus Phyllomedusa (P. oreades and P. distincta),^[67] the sesquiterpene lactone dehydroleucodine (DhL), which affects the growth of cultured epimastigote-phase Trypanosoma cruzi,^[68] inhibitors of purine uptake,^[64] and inhibitors of enzymes involved in trypanothione metabolism.^[69] Hopefully, new drug targets may be revealed following the sequencing of the T. cruzi genome.^[70]

Chagas disease has a serious economic impact on the United States and the world. The cost of treatment in the United States is estimated to be $900 million annually, which includes hospitalization and medical devices such as pacemakers. The global cost is estimated at $7 billion.^[71]

Megazol in a study seems more active against Chagas than benznidazole but has not been studied in humans.^[72] Fexinidazole, an old drug rediscovered for this purpose is being tested in phase 2 clinical trials.^[73] A Chagas vaccine (TcVac3) has been found to be effective in mice with plans for studies in dogs. It is hoped that it will be commercially available by 2018.^[74]

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^ Dumonteil E, Escobedo-Ortegon J, Reyes-Rodriguez N, Arjona-Torres A, Ramirez-Sierra M (2004). "Immunotherapy of Trypanosoma cruzi Infection with DNA Vaccines in Mice". Infect Immun 72 (1): 46–53. doi:10.1128/IAI.72.1.46-53.2004. PMC 343959. PMID 14688079.
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External links

Chagas disease at DMOZ
Chagas information at the U.S. Centers for Disease Control
Chagas information from the Drugs for Neglected Diseases initiative
Norma Andrews's seminar: Trypanosoma cruzi and Chagas Disease
UNHCO site on Chagas Disease
Chagas Disease information for travellers from IAMAT (International Association for Medical Assistance to Travellers)

UpToDate Contents

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1. シャガス病：急性と先天性のクルーズトリパノソーマ感染症chagas disease acute and congenital trypanosoma cruzi infection [show details]
… Chagas disease is caused by infection with the protozoan parasite Trypanosoma cruzi; the major manifestations are Chagas cardiomyopathy and gastrointestinal disease . Issues related to acute and congenital …
2. シャガス病：慢性クルーズトリパノソーマ感染症chagas disease chronic trypanosoma cruzi infection [show details]
… Chagas disease is caused by infection with the protozoan parasite Trypanosoma cruzi; the major manifestations are Chagas cardiomyopathy and gastrointestinal disease . Issues related to the natural history …
3. 慢性シャーガス心筋症：臨床症状と診断chronic chagas cardiomyopathy clinical manifestations and diagnosis [show details]
… Chagas disease (CD) is caused by Trypanosoma cruzi, a protozoan parasite that can cause acute myopericarditis as well as chronic fibrosing myocarditis. CD is the most common cause of non-ischemic cardiomyopathy …
4. シャガス病：疫学および予防chagas disease epidemiology and prevention [show details]
…epidemiology and prevention of Chagas disease will be reviewed here. Other issues related to Chagas disease are discussed in detail separately: Chagas disease is responsible for a higher burden …
5. 消化管のシャーガス病chagas gastrointestinal disease [show details]
… Chagas disease is caused by infection with the protozoan parasite Trypanosoma cruzi; the major manifestations are Chagas cardiomyopathy and gastrointestinal disease . Issues related to the epidemiology …

English Journal

Analysis of bioactivities and chemical composition of Ziziphus joazeiro Mart. using HPLC-DAD.

Brito SM1, Coutinho HD2, Talvani A3, Coronel C4, Barbosa AG1, Vega C4, Figueredo FG5, Tintino SR5, Lima LF5, Boligon AA6, Athayde ML6, Menezes IR7.
Food chemistry.Food Chem.2015 Nov 1;186:185-91. doi: 10.1016/j.foodchem.2014.10.031. Epub 2014 Oct 17.
The aim of this study was to evaluate the chemical profile and antioxidant, antimicrobial and antiparasitic activities of the hydroalcoholic extract of the leaves of Ziziphus joazeiro Mart. (HELZJ). The antioxidant DPPH and FRAP assays and chemical profile were determined by colorimetric methods and
PMID 25976809

Diagnosis of congenital Trypanosoma cruzi infection: A serologic test using Shed Acute Phase Antigen (SAPA) in mother-child binomial samples.

Volta BJ1, Russomando G2, Bustos PL1, Scollo K1, De Rissio AM1, Sánchez Z3, Cardoni RL1, Bua J4.
Acta tropica.Acta Trop.2015 Jul;147:31-7. doi: 10.1016/j.actatropica.2015.03.026. Epub 2015 Apr 3.
Chagas congenital infection is an important health problem in endemic and non-endemic areas in which Trypanosoma cruzi-infected women can transmit the parasite to their offspring. In this study, we evaluated the antibody levels against the T. cruzi Shed Acute Phase Antigen (SAPA) in 91 binomial samp
PMID 25847262

Effect of pacemaker site on B-type natriuretic peptide levels and left ventricular function in a population with high prevalence of Chagas disease.

de Souza SF1, Nascimento BR2, Nunes Mdo C3, da Silva JL4, de Carvalho VT5, Beaton AZ6, Rocha MO3, Ribeiro AL3.
International journal of cardiology.Int J Cardiol.2015 Jul 1;190:315-8. doi: 10.1016/j.ijcard.2015.04.127. Epub 2015 Apr 17.
PMID 25935619

Related Pictures

★リンクテーブル★

リンク元	「シャーガス病」「アメリカトリパノソーマ症」「Americanトリパノソーマ症」
関連記事	「American」「America」

「シャーガス病」

Chagas disease
	Photomicrograph of Giemsa-stained Trypanosoma cruzi
Classification and external resources
Specialty	Infectious disease
ICD-10	B57
ICD-9-CM	086
DiseasesDB	13415
MedlinePlus	001372
eMedicine	med/327
Patient UK	Chagas disease
MeSH	D014355

　　[★]

英: Chagas disease, Chagas' disease
同: Chagas病
関: アメリカトリパノソーマ病アメリカ・トリパノソーマ症 American trypanosomiasis、スキゾトリパノソーマ症 schizotrypanosomiasis、ブラジル・トリパノソーマ症 Brazilian trypanosomiasis、シャーガス-クルース病 Chagas-Cruz disease; トリパノソーマ属、原虫

アメリカでは感染者は献血が制限される
クルース・トリパノソーマ Trypanosoma cruziの感染
人獣共通感染症

特徴

ウイルス学

病原体

クルース・トリパノソーマ Trypanosoma cruzi

疫学

南アメリカ、中央アメリカ

潜伏期間

感染経路

サシガメ(Triatoma)の糞中に排出される感染型虫体から皮膚・眼の結膜へ

皮膚
眼の結膜　→　eye edema ロマニャ徴候

症状

拡張型心筋症、巨大結腸、巨大食道
慢性期に移行しやすい(初期に見つかるのは感染者のうち1-2%)。
多くの場合発熱を呈する
初期：

原虫侵入部の腫脹と領域リンパ節の腫脹
(眼の結膜)ロマニャ徴候

全身への移行：筋組織を好む

乳児では脳炎、心筋炎が重症化しやすい

脳：脳炎
心臓：不整脈、拡張型心筋症
筋肉：心筋炎

合併症

経過

無症状期：10-20年の無症状期
発症　　：抗体陽性者の半数以上が心症状(拡張型心筋症)、消化器症状(巨大食道、巨大結腸)を呈する

治療

nifurtimox

検査

予防

-Chagas病

「アメリカトリパノソーマ症」

　　[★]

英: American trypanosomiasis
関: シャーガス病、Americanトリパノソーマ症

「Americanトリパノソーマ症」

　　[★]

英: American trypanosomiasis
関: アメリカトリパノソーマ症

「American」

　　[★]

アメリカの、アメリカ人

関: America

「America」

　　[★]

n.

アメリカ、米国

関: American、USA

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[pmid18660992-30] Basso B, Moretti E, Fretes R (June 2008). "Vaccination with epimastigotes of different strains ofTrypanosoma rangeli protects mice against Trypanosoma cruzi infection". Mem Inst Oswaldo Cruz 103 (4): 370–4. doi:10.1590/S0074-02762008000400010. PMID 18660992.

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Chagas disease
Photomicrograph of Giemsa-stained Trypanosoma cruzi
Classification and external resources
Specialty	Infectious disease
ICD-10	B57
ICD-9-CM	086
DiseasesDB	13415
MedlinePlus	001372
eMedicine	med/327
Patient UK	Chagas disease
MeSH	D014355

匿名

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案内

American trypanosomiasis