Evaluation on The Levels Of Liver Function Enzymes In Type 2 Diabetics With Malaria Parasite Infection

 – Evaluation on the Levels of Liver Function Enzymes in Type 2 Diabetics with Malaria Parasite Infection – 

Download Evaluation on the Levels of Liver Function Enzymes in Type 2 Diabetics with Malaria Parasite Infection project materials: This project material is ready for students who are in need of it to aid their research.

INTRODUCTION

Type 2 diabetes mellitus is a long term metabolic disorder that is characterized by high blood glucose, insulin resistance and relative lack of insulin (Pasquel and Umpierrez, 2014).

The insulin resistance is the inability of cells to respond adequately to normal levels of insulin and this occurs primarily within the muscles,  liver and fat tissue.

The proportion of insulin resistance versus beta cell dysfunction differs among individuals with some having primarily insulin resistance and only a minor defect in insulin secretion and others with slight insulin and primarily a lack of insulin secretion(Maruthur  et al.,  2016).

There are usually symptoms associated with type 2 diabetes mellitus which include: increased thirst, frequent urination, weight loss, increased hunger, feeling tired and having wounds that dont heal (Zaccardi et al., 2016).

Malaria is a mosquito borne infectious disease that affects humans and other animals. It is caused by parasitic protozoans belonging to the plasmodium type.

The disease is commonly transmitted by an infected female anopheles mosquito.The species of plasmodium that cause malaria are: plasmodium vivax, plasmodium falciparum, plasmodium ovale, plasmodium malaria and plasmodium knowleski.

In all these, the plasmodium falciparum is the most common. (Cowman et al.,2012). The mosquito causes an infection by a bite. First, sporozoites enter the blood stream and migrate to the liver.

They infect the liver cells where they develop into ring forms trophozoites and schizonts that in turn produce further merozoites. Sexual forms are also produced within, if taken up by a mosquito will infect the insect and continue the life cycle, (Vaughan et al., 2008).

REFERENCES

Abdel Misih, S.R And Bloomston M. (2010): “Liver anatomy” surgical clinics of North America. 90(4): 643-53

Abu –Raddad L., Patrck .P., Kublin J. (2006): Dual infection with HIV and malaria, fuels the spread of  both  diseases in sub-Saharan Africa .Sciene 314: 1603-6

Anderson, G.C., Morton, C. Green, I.(2001).  Parasites  and  human diseases in community health. 3rd edition, Churchill Livingstone, U.S.A, Pp: 45-68

Arrow, K.J., Panasian, C., Gelband, H. (2008): Saving lives; buying times; Economics of malarial drugs in an age of resistance.4th edition. Pp 141

Ashley, M.V., Ahmed, S.A., Stefan ,H.T, Kappe (2008). “Malaria parasite pre-erythrocytic stage infection, gling and hiding cell host microbe, 2008; 4(3): 209-218.

Bagdade, J.D, Bierman, E.L, Porte ,D. Jr. The significance of basal insulin levels in the evaluation of the insulin response to glucose in diabetic and non-diabetic subjects. Journal of clinical investigation.(2008). 46: 1549-1557.

Bartoloni ,A., Zammarachi, L. (2012). “Clinical aspects of uncomplicated and severe malaria”. Mediterranean Journal of Hematology and Infectious Diseases 4(1): 2012-026.

Be the first to comment

Leave a Reply

Your email address will not be published.


*