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Incidence of Human Plasmodiasis in Northern and Southern Districts of Khyber Pakhtunkhwa, Pakistan

PJZ_50_4_1585-1588

 

 

Incidence of Human Plasmodiasis in Northern and Southern Districts of Khyber Pakhtunkhwa, Pakistan

Muhammad Asim Khan1,*, Shahid Niaz Khan1, Sanaullah Khan2, Abdul Jabbar Khan3, Muhammad Adnan4, Nawab Ali5 and Ijaz Ali6

1Department of Zoology, Kohat University of Science and Technology, Kohat 26000

2Department of Zoology, University of Peshawar, Peshawar

3Department of Biological Sciences, Gomal University, D.I. Khan

4Department of Botany, Kohat University of Science and Technology, Kohat 26000

5Department of Biotechnology and Genetic Engineering, Kohat University of Science and Technology, Kohat 26000

6Department of Biosciences, COMSATs Institute of Information Technology, Islamabad

ABSTRACT

Total 3968 blood films were prepared from various age groups ranging from below 1 year up to above 50 years during the months of June 2010 to June 2012, residing in Northern (Peshawar, Mardan, Charsaddah, Sawabi, Nowshehra) and Southern (Bannu, Lakki, Karrak, Kohat, D.I.Khan) districts of Khyber Pakhtunkhwa, Pakistan. All the films were examined by microscopy for the detection of malarial parasites. In the Southern districts, the overall incidence of Plasmodium slides positivity was 52.47% of which 91.07% were identified as Plasmodium vivax and 6.23% as P. falciparum and 2.69 was 43.62%, of which Plasmodium vivax were 91.2%, Plasmodium falciparum were 6.09% and 2.68% were identified as mixed infections. Malaria was most prevalent in the age group 11 - 20 years (61.68 %,) and 40 -50 > (81.63%) years patients. The results also showed that highest infection (72.56%) was found in the month of August and (68.52%) in September, while the lowest prevalence of malaria infection was found in the months of December (7.93%) and in February (12.62%).


Article Information

Received 13 May 2016

Revised 22 June 2017

Accepted 12 January 2018

Available online 07 June 2018

Authors’ Contributions

MAK collected the samples, designed the study and performed microscopic analysis. SNK, SK, MA, NA, IA and AJK helped in manuscript writing and statistically analysis.

Key words

Malaria, P. falciparum, P. vivax, Plasmodiasis.

DOI: http://dx.doi.org/10.17582/journal.pjz/2018.50.4.sc14

* Corresponding author: asim_997@yahoo.com

0030-9923/2018/0004-1585 $ 9.00/0

Copyright 2018 Zoological Society of Pakistan



Malaria is a vector-borne infectious disease caused by protozoan parasite of the genus Plasmodium (Snow et al., 2005). Plasmodium is primarily transmitted by the bite of an infected female Anopheles mosquito, but infections can also occur through exposure to infected blood Products (transfusion malaria) and by congenital transmission (Trampuz et al., 2003). Plasmodium has different species. P. vivax and P. falciparum are the common species detected in human disease. Other species are less common. Malaria occurs throughout the year. Prevalence of malaria shows seasonal variation (Jan and Kiani, 2001).

At present 109 countries are endemic for malaria, out of which 45 countries are within the African region (WHO, 2009). Outside Africa, it is a major public health problem and important contributor to the global burden of morbidity (Yang et al., 2006). More than 90% of cases of malarial deaths occur in tropical Africa. Poorest countries are suffering with burden of malaria (Panda and Mohapatra, 2004). In European countries most cases are due to P. malariae and P. vivax (Voittier et al., 2008). South East Asia and India contribute about 70% of the total malaria cases (Dash et al., 2008).

Vivax malaria is a major health problem in Pakistan. In the last decade there has been a six fold increase in falciparum malaria, which now comprises 42% of all malaria cases recorded by National Malaria Control Program (MCP) (Shah et al., 1997). Factors associated with the upsurge include of chloroquine resistance across the country (Shah et al., 1997), warmer autumns favoring prolonged transmission (Bouma et al., 1996), and a chronic decline in vector control activities. Anopheles culicifacies, the purported primary vector in the Punjab province (Reisen and Boreham, 1982), disappeared by September, whereas A. stephensi was found more abundant in North-West Frontier Province (presently Khyber Pakhtunkhwa) than A. culicifacies. In Pakistan (Duki, Harnai and Sibi), the primary vector species are A. culicifacies and A. stephensi (MCP, 1999, 2006). In this study, we report incidence of Plasmodium in northern and southern districts of Khyber Pakhtunkhwa.

Materials and methods

After informed consent of the subjects a total of 3968 blood smears, both thick and thin, were prepared for the detection of malarial parasites. The current study was carried out in southern districts (Bannu, Lakki, Karak, Kohat, D.I. Khan) and northern districts (Peshawar, Mardan, Charsaddah, Sawabi, Nowshehra) of Khyber Pakhtunkhwa during June 2010 to June 2012. Blood smears were fixed in methyl alcohol and then stained in Giemsa stain for 20-30 min. The slides were screened under microscope for the detection of malarial parasites.

 

Results and discussion

Table I shows overall incidence of Plasmodium prevalence in Southern and Northern districts of Khyber Pakhtunkhwa. Out of total 52.47% prevalence in southern districts 91.07% identified as P. vivax, 6.23% as P. falciparum and 2.69% as mixed infections. In the northern districts the overall incidence of Plasmodium was 43.62% of which P. vivax contributed 91.2%, P. falciparum 6.09% and mixed infections 2.68%.

Similar type of study in India showed 7.2% population in Gujrat infected with Plamodium, of which 72.47.% were identified as P. vivax, 24.1% cases were P. falciparum and 3.44% cases were mixed infections (Trivedi et al., 2010). Similarly, Zarchi et al. (2006) observed infection of Plasmodium in Iranian parts of south-east of Caspian Sea and detected that P. vivax was 61%, P. falciparum was 20.7% and mixed infection was 18.3%, respectively. Yasinzai and Kakar (2012) showed high incidence of P. vivax (81%) and P. falciparum (18.9%) in Jaffarabad district.

Idris et al. (2007) reported 7.2% positive cases in Abbottabad of which P. vivax contributed 72.47%, P. falciparum 24.1% and mixed infection was observed 3.44% cases. Akbar et al. (2006) observed high prevalence of malarial parasites (96.2%) in children of Mansehra, in which P. vivax was 92.2%, and P. falciparum was 7.7%. Jan and Kiani (2001) also observed high incidence of P. vivax (6.33%) compared to P. falciparum (0.67%) in Kashmiri refugees of Muzaffarabad.

Table II shows age wise incidence of Plasmodium. The overall highest incidence was in the age group of 41-45 years (81.63%) followed by age groups 11-20 (61.68%) and 21-30 (47.18%). Age group <1-10 was least affected (22.78%). In all of them P. vivax was the most dominant infection.

Table III shows incidence of plasmodiasis during different season of the year. Highest slides positivity rate (SPR) was observed in August (72.56%) and September (68.52%) and lowest in December (7.93%) and in February (12.62%). From among southern districts high SPR of P. vivax was 92.4% observed in Bannu district followed by 89.7% in Kohat and 89.7% in D.I. Khan, P. falciparum on the other hand showed 8.1% incidence in D.I. Khan and 3.4% in Bannu. Likewise in northern districts P. vivax showed 92.93% SPR in Peshawar followed by 80.76% in Nowshehra district, P. falciparum showed 19.23% incidence in Nowshehra and 2.8% in Charsadda.

 

Table I.- Overall incidence of malarial parasites in Southern and Northern districts of Khyber Pakhtunkhwa.

Areas

Slides examined

No. of positive (%)

P. vivax (%)

P. falciparum (%)

Mixed (%)

Southern districts

Bannu

782

409 (52.3)

378 (92.4)

14 (3.4)

17 (4.1)

Lakki

448

192 (42.8)

176 (91.6)

11 (5.7)

5 (2.6)

Karak

411

166 (40.38)

153 (92.1)

13 (7.8)

0 (0.0)

Kohat

385

215 (55.8)

193 (89.7)

15 (6.9)

7 (3.2)

D.I. Khan

663

429 (64.7)

385 (89.7)

35 (8.1)

9 (2.69)

Total

2689

1411 (52.4)

1285 (91.1)

88 (6.2)

38 (2.7)

Northern districts

Peshawar

673

354 (52.6)

322 (90.9)

21 (5.9)

11 (3.1)

Mardan

174

48 (27.58)

42 (87.5)

6 (12.5)

0 (0.0)

Charsadda

203

98 (48.2)

93 (88.5)

3 (2.8)

2 (1.9)

Sawabi

158

32 (20.2)

27 (84.3)

3 (9.3)

2 (6.2)

Nowshehra

71

26 (36.6)

25 (96.1)

1 (3.8)

0 (0.0)

Total

1279

558 (43.6)

509 (91.2)

34 (6.09)

15 (2.68)

 

Table II.- Age wise over all incidence of malarial parasites in Northern and Southern districts of Khyber Pakhtunkhwa.

Age groups

Slides examined

Over all infection (%)

P. vivax (%)

P. falciparum (%)

Mixed (%)

<1-10

891

203 (22.78)

203 (100)

0 (0.00)

0 (0.00)

11-20

1172

723 (61.68)

656 (90.73)

45 (6.22)

22 (3.04)

21-30

907

428 (47.18)

401 (93.69)

19 (4.43)

8 (1.86)

31-40

388

117 (30.15)

87 (74.35)

21 (17.94)

9 (7.69)

41-50>

610

498 (81.63)

447 (89.75)

37 (7.42)

14 (2.81)

Total

3968

1769 (49.62)

1794 (91.11)

122 (6.19)

53 (2.69)

 

Table III.- Month wise incidence of malarial parasites in Northern and Southern districts of Khyber Pakhtunkhwa.

Month

Slides examined

Over all infection (%)

P. vivax (%)

P. falciparum (%)

Mixed (%)

June 2010

779

363 (46.59)

359 (98.89)

4 (1.1)

0 (0)

July

653

434 (66.46)

411 (94.70)

21 (4.83)

2 (0.46)

August

401

291 (72.56)

237 (81.44)

37 (12.71)

17 (5.84)

September

664

455 (68.52)

393 (86.37)

39 (8.57)

23 (5.05)

October

225

140 (62.22)

133 (95.0)

4 (2.85)

3 (2.14)

November

131

38 (29.0)

37 (97.36)

1 (2.63)

0 (0.0)

December

189

15 (7.93)

13 (86.66)

2 (13.33)

0 (0.0)

January

121

26 (21.48)

26 (100)

0 (0.0)

0 (0.0)

February

103

13 (12.62)

12 (92.30)

1 (7.69)

0 (0.0)

March

137

32 (23.35)

32 (100)

0 (0.0)

0 (0.0)

April

197

47 (23.85)

43 (91.48)

4 (8.52)

0 (0.0)

May

107

33 (30.84)

31 (93.93)

2 (6.7)

0 (0.0)

June 2012

261

82 (31.41)

67 (81.70)

7 (8.53)

8 (9.75)

Total

3968

1969

1794 (91.11)

122 (6.19)

53 (2.69)

 

Similar type of study was done by Toma et al. (2001), in Laos, in which the prevalence rate of malarial parasites in less than 10 years was 40.7%, 11 to 20 years 52.4%, 21 to 30 years 28.6%, 31 to 40 years 25.0%, 41 to 50 years 7.1% and >50 years 26.3%. Yasinzai and Kakar (2012) reported 32.8% in 1-10 years, 50.6% 11-20 years and 51.5% in the age group of 21 years and above. Likewise Idris et al., (2007) reported 48.27% infection in <15 years age group, 8.96% in 15-30 years, 5.51% in 30-45 years, 16.55% in 45-60 years, 13.79% in 60-80 years and 6.89% in 80 years age group.

In the study percentages of infections is more in 11-20 and 41-50> years age groups, because at that stage children are more exposed to environment, and percentage of infections was high in old age persons are due to low immune response. Similar result has been found by Ali et al. (2013) at district Charsada, adolescence 11-20 years were more infected (22.8%) than younger (1-10 years) and old aged above thirty years were highly (39%) infected.

Seasonal variations were also observed in Khyber Pakhtunkhwa, Pakistan. In the present study high percentage of infection was observed in August (72.56%) and September (68.52%) and lowest in December (7.93%) and February (12.62%). While, Yasinzai and Kakar (2012) observed high percentage of infection was in May (56.8%) and lowest in June (35.2%) in Jafffarabad. High percentage of infections (57.90%) in September and lowest (25.33%) in January detected by Mohammad and Hussain (2003) in Buner district. The differences in the above mentioned studies are due to number of samples, hygienic conditions of the areas, immune response and temperature of the areas etc.

 

Conclusion

It was concluded that there were significant risk factors for malaria prevalence. The poor hygienic condition, no use of antimalarials sprays, use of irrigated land, sharing the house with livestock, improper diagnosis, high temperature of the area and load shading also play a key role for the spread of malaria in both Southern and Northern belt of Khyber Pakhtunkhwa, Pakistan.

 

Acknowledgement

The authors are highly obliged for the cooperation of all Laboratories Incharge and Laboratories Assistant of all the Hospitals of Northern and Southern Districts.

 

Statement of conflict of interest

Author has declared that no competing interests exist.

 

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