Raised plasma insulin level and homeostasis model assessment (HOMA) score in cerebral malaria: evidence for insulin resistance and marker of virulence

被引:0
作者
Eltahir, Elrashid M. [1 ,2 ]
ElGhazali, Gehad [1 ,2 ,3 ]
A-Elgadir, Thoraya M. E. [1 ,2 ]
A-Elbasit, Ishraga E. [1 ,2 ]
Elbashir, Mustafa I. [1 ,2 ]
Giha, Hayder A. [1 ,2 ,4 ]
机构
[1] Univ Khartoum, Fac Med, MalRC, Dept Biochem, Khartoum, Sudan
[2] Univ Khartoum, Fac Med, Dept Microbiol, Khartoum, Sudan
[3] King Fahad Med City, Riyadh, Saudi Arabia
[4] AGU, Dept Med Biochem, Fac Med & Med Sci, Manama, Bahrain
关键词
cerebral malaria; hyperglycaemia; HOMA; insulin resistance; virulence; PLASMODIUM-FALCIPARUM; GLUCOSE; HYPOGLYCEMIA; AREA; COMPLICATIONS; ERYTHROCYTES; TURNOVER; KINETICS; CHILDREN; ADULTS;
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Objective: To study the glycaemic profile of patients with severe malaria (SM). Methods: For this purpose, 110 SM patients were recruited. Pre-treatment random blood glucose and plasma insulin were measured in a subset of donors. An ex-vivo experiment was developed for estimation of glucose consumption by parasitized erythrocytes. Results: Hyperglycaemia was frequent in SM but more commonly associated with cerebral malaria (CM), while hyperinsulinaemia was recognized in severe-malarial-hypotension (median, 25 %-75 %, 188.2, 93.8-336.8 pmol/L). The plasma insulin level was positively correlated with age (CC=0.457, P<0.001) and negatively with parasitaemia (CC=-0.368, P=0.045). Importantly, fatal-CM was associated with hyperglycaemia (12.22, 6.5-14.6 mmol/L), hyperinsulinaemia (141.0, 54.0-186.8 pmol/L) and elevated homeostasis model assessment (HOMA) values. However, there was a trend of higher glucose consumption by parasites in CM compared with that in uncomplicated malaria (UM). Conclusion: Hyperglycaemia, hyperinsulinaemia and elevated HOMA are evidence for insulin resistance and possibly pancreatic B-cell dysfunction in fatal-CM.
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页码:513 / 520
页数:8
相关论文
共 35 条
[1]   Allelic polymorphism of MSP2 gene in severe P-falciparum malaria in an area of low and seasonal transmission [J].
A-Elbasit, Ishraga E. ;
ElGhazali, Gehad ;
A-Elgadir, Thoraya M. E. ;
Hamad, Amel A. ;
Babiker, Hamza A. ;
Elbashir, Mustafa I. ;
Giha, Hayder A. .
PARASITOLOGY RESEARCH, 2007, 102 (01) :29-34
[2]   Glucose and lactate kinetics in children with severe malaria [J].
Agbenyega, T ;
Angus, BJ ;
Bedu-Addo, G ;
Baffoe-Bonnie, B ;
Guyton, T ;
Stacpoole, PW ;
Krishna, S .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2000, 85 (04) :1569-1576
[3]  
Beales PF, 2000, T ROY SOC TROP MED H, V94, pS1
[4]   Glucose metabolism in severe malaria: Minimal model analysis of the intravenous glucose tolerance test incorporating a stable glucose label [J].
Binh, TQ ;
Davis, TME ;
Johnston, W ;
Thu, LTA ;
Boston, R ;
Danh, PT ;
Anh, TK .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1997, 46 (12) :1435-1440
[5]   The uncertain burden of Plasmodium falciparum epidemics in Africa [J].
Cox, Jonathan ;
Hay, Simon I. ;
Abeku, Tarekegn A. ;
Checchi, Francesco ;
Snow, Robert W. .
TRENDS IN PARASITOLOGY, 2007, 23 (04) :142-148
[6]   Glucose and lactate turnover in adults with falciparum malaria: effect of complications and antimalarial therapy [J].
Davis, TME ;
Binh, TQ ;
Thu, LTA ;
Long, TTA ;
Johnston, W ;
Robertson, K ;
Barrett, PHR .
TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 2002, 96 (04) :411-417
[7]   GLUCOSE-TURNOVER IN SEVERE FALCIPARUM-MALARIA [J].
DAVIS, TME ;
LOOAREESUWAN, S ;
PUKRITTAYAKAMEE, S ;
LEVY, JC ;
NAGACHINTA, B ;
WHITE, NJ .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1993, 42 (03) :334-340
[8]   Membrane modifications in erythrocytes parasitized by Plasmodium falciparum [J].
Deitsch, KW ;
Wellems, TE .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1996, 76 (1-2) :1-10
[9]   Acidosis in severe childhood malaria [J].
English, M ;
Sauerwein, R ;
Waruiru, C ;
Mosobo, M ;
Obiero, J ;
Lowe, B ;
Marsh, K .
QJM-AN INTERNATIONAL JOURNAL OF MEDICINE, 1997, 90 (04) :263-270
[10]   Drug resistance-virulence relationship in Plasmodium falciparum causing severe malaria in an area of seasonal and unstable transmission [J].
Giha, HA ;
Elbashir, MI ;
A-Elbasit, IE ;
A-Elgadit, TME ;
ElGhazali, GE ;
Mackinnon, MJ ;
Babiker, HA .
ACTA TROPICA, 2006, 97 (02) :181-187