1.Drug Resistance and in Vitro Susceptibility of Plasmodium falciparum in Thailand during 1988-2003.
Nantana SUWANDITTAKUL ; Wanna CHAIJAROENKUL ; Pongchai HARNYUTTANAKORN ; Mathirut MUNGTHIN ; Kesara NA BANGCHANG
The Korean Journal of Parasitology 2009;47(2):139-144
The aim of the present study was to investigate antimalarial drug pressure resulting from the clinical use of different antimalarials in Thailand. The phenotypic diversity of the susceptibility profiles of antimalarials, i.e., chloroquine (CQ), quinine (QN), mefloquine (MQ), and artesunate (ARS) in Plasmodium falciparum isolates collected during the period from 1988 to 2003 were studied. P. falciparum isolates from infected patients were collected from the Thai-Cambodian border area at different time periods (1988-1989, 1991-1992, and 2003), during which 3 different patterns of drug use had been implemented: MQ + sulphadoxine (S) + pyrimethamine (P), MQ alone and MQ + ARS, respectively. The in vitro drug susceptibilities were investigated using a method based on the incorporation of [3H] hypoxanthine. A total of 50 isolates were tested for susceptibilities to CQ, QN, MQ, and ARS. Of these isolates, 19, 16, and 15 were adapted during the periods 1988-1989, 1991-1993, and 2003, respectively. P. falciparum isolates collected during the 3 periods were resistant to CQ. Sensitivities to MQ declined from 1988 to 2003. In contrast, the parasite was sensitive to QN, and similar sensitivity profile patterns were observed during the 3 time periods. There was a significantly positive but weak correlation between the IC50 values of CQ and QN, as well as between the IC50 values of QN and MQ. Drug pressure has impact on sensitivity of P. falciparum to MQ. A combination therapy of MQ and ARS is being applied to reduce the parasite resistance, and also increasing the efficacy of the drug.
Animals
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Antimalarials/*pharmacology/therapeutic use
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Artemisinins/pharmacology/therapeutic use
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Chloroquine/pharmacology/therapeutic use
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*Drug Resistance
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Humans
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Malaria/drug therapy/*parasitology
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Mefloquine/pharmacology/therapeutic use
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Parasitic Sensitivity Tests/methods
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Plasmodium falciparum/*drug effects/isolation & purification
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Quinine/pharmacology/therapeutic use
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Thailand
2.First Report of Neutrophil Involvement of Exflagellated Plasmodium vivax Microgametes.
Soo In CHOI ; Byung Ryul JEON ; Yong Wha LEE ; Hee Bong SHIN ; You Kyoug LEE
Annals of Laboratory Medicine 2014;34(6):481-483
No abstract available.
Adult
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Anti-Bacterial Agents/therapeutic use
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Antimalarials/therapeutic use
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Clindamycin/therapeutic use
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Female
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Humans
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Malaria, Vivax/*diagnosis/drug therapy/parasitology
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Neutrophils/*parasitology
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Plasmodium vivax/growth & development/*isolation & purification
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Pregnancy
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Quinine/therapeutic use
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Trophozoites/cytology
3.Immunoglobulin A Nephropathy Associated with Plasmodium falciparum Malaria.
Dong Eun YOO ; Jeong Ho KIM ; Jeong Hae KIE ; Yoonseon PARK ; Tae Ik CHANG ; Hyung Jung OH ; Seung Jun KIM ; Tae Hyun YOO ; Kyu Hun CHOI ; Shin Wook KANG ; Seung Hyeok HAN
Journal of Korean Medical Science 2012;27(4):446-449
Glomerulonephritis occurs as a rare form of renal manifestation in Plasmodium falciparum malaria. Herein, we report a case of falciparum malaria-associated IgA nephropathy for the first time. A 49-yr old male who had been to East Africa was diagnosed with Plasmodium falciparum malaria. Microhematuria and proteinuria along with acute kidney injury developed during the course of the disease. Kidney biopsy showed mesangial proliferation and IgA deposits with tubulointerstitial inflammation. Laboratory tests after recovery from malaria showed disappearance of urinary abnormalities and normalization of kidney function. Our findings suggest that malaria infection might be associated with IgA nephropathy.
Acute Kidney Injury/etiology/pathology
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Antimalarials/therapeutic use
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Creatinine/blood
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Glomerulonephritis, IGA/*diagnosis/*etiology
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Hematuria/etiology
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Humans
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Immunoglobulin A/*metabolism
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Malaria/*complications/drug therapy/*pathology
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Male
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Middle Aged
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Plasmodium falciparum/*isolation & purification
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Proteinuria/etiology
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Quinine/therapeutic use
4.A History of Malaria in Modern Korea 1876-1945.
Korean Journal of Medical History 2011;20(1):53-82
Although it is not certain when malaria began to appear in Korea, malaria is believed to have been an endemic disease from ancient times. It was Dr. H. N. Allen (1858-1932) who made the first description and diagnosis of malaria in terms of Western medicine. In his first year report (1885) of Korean Government Hospital he mentioned malaria as the most prevalent disease. Very effective anti-malarial drug quinine was imported and it made great contribution in treating malaria. After Japan had annexed Korea in 1910, policies for public health system were fundamentally revised. Japan assumed control of Korean medical institutions and built high-quality Western hospitals for the health care of Japanese residents. The infectious diseases which were under special surveillance were cholera, typhoid fever, dysentery, typhus, scarlet fever, smallpox, and paratyphoid fever. Among chronic infectious diseases tuberculosis and leprosy were those under special control. Malaria, however, was not one of these specially controlled infectious diseases although it was widely spread throughout the peninsula. But serious studies on malaria were carried out by Japanese medical scientists. In particular, a Japanese parasitologist Kobayasi Harujiro(1884-1969) carried out extensive studies on human parasites, including malaria, in Korea. According to his study, most of the malaria in Korea turned out to be tertian fever. In spite of its high prevalence, malaria did not draw much attention from the colonial authorities and no serious measure was taken since tertian fever is a mild form of malaria caused by Plasmodium vivax and is not so much fatal as tropical malaria caused by P. falciparum. And tertian malaria was easily controlled by taking quinine. Although the majority of malaria in Korea was tertian fever, other types were not absent. Quartan fever was not rarely reported in 1930s. The attitude of colonial authorities toward malaria in Korea was contrasted with that in Taiwan. After Japan had set out to colonize Taiwan as a result of Sino-Japanese war, malaria in Taiwan was a big obstacle to the colonization process. Therefore, a lot of medical scientists were asked to engage the malaria research in order to handle health problems in colonized countries caused by malaria. Unlike the situation in Taiwan, malaria in Korea did not cause a serious health problem as in Taiwan. However, its risk was not negligible. In 1933 there were almost 130,000 malaria patients in Korea and 1,800 patients among them died of malaria. The Japanese Government General took measures to control malaria especially during the 1930s and the number of patients decreased. However, as Japan engaged in the World War II, the general hygienic state of the society worsened and the number of malarial patients increased. The worsened situation remains the same after Liberation (1945) and during the Korean war (1950-53).
Colonialism/history
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History, 19th Century
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History, 20th Century
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Humans
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Korea
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Malaria/diagnosis/drug therapy/*history
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Malaria, Vivax/diagnosis/drug therapy/history
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Microscopy, Polarization
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Plasmodium malariae/isolation & purification
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Plasmodium ovale/isolation & purification
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Plasmodium vivax/isolation & purification
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Quinine/history/therapeutic use