Cannabis Abuse and Hematological Variations to Endorse Severe Health Implications Among Kashmiri Youth
Irfan Ahmad Wani*1, Bhupinder Singh2 and Muzafer Ahmad Khan3
1 Research Scholar utd, Barkatullah University Bhopal M.P, India
2 Professor utd, Barkatullah University Bhopal M.P, India
3 Director Drug De-Addiction and Rehabilitation Centre Police Control Srinagar Kashmir, India
Submission: July 13, 2018; Published: July 17, 2018
*Corresponding author: Irfan Ahmad Wani, Research Scholar utd Barkatullah University Bhopal M.P India, Tel: 917006558529; Email: wanipsy@gmail.com
How to cite this article: Irfan AW Bhupinder S, Muzafer AK. Cannabis Abuse and Hematological Variations to Endorse Severe Health Implications Among Kashmiri Youth. JOJ Nurse Health Care. 2018; 8(4): 555745. DOI: 10.19080/JOJNHC.2018.08.555745.
Abstract
The present study is conceded out to scrutinize the effect of cannabis abuse on blood composition of cannabis abusers in contrast with control group of Kashmiri youth by taking complete blood count test to figure out the occurrence of hematological variations which are typical cause of health pathology. The sample consisted of 300 male patients on which CBC test was taken of these 150 were belong to cannabis abusers and rest were belong to control group. The result of the study showed that two groups significantly differed on Hemoglobin, Hematocrit, RBC count, platelet count, total Leucocyte count, Neutrophils, Lymphocytes, Monocytes, Eosionophills, Basophil, absolute Neutrophil count, absolute Lymphocytes count, absolute Monocyte count, absolute Eosionophil count, absolute Basophills and glucose fasting. While in MCV, MCH, MCHC and RDW-CV contents remain non-significant among cannabis abusers.
Keywords: Cannabis abuse; Haematology; Thromboembolism and hypochromia
Abbrevations:MCV: Mean Corpuscular Volume; MCH: Mean Corpuscular Hemoglobin; MCHC: Mean Corpuscular Hemoglobin Concentration
Introduction
The most contentious use of the cannabis sativa plant is for its psychoactive properties a chemical namely Delta-9-tetrahydriocannabinol (THC) Ebuehi OAT [1]. Cannabis smoke contains various chemicals, including THC, carbon monoxide and carcinogens (substances that cause cancer) (British Medical Association BMA [2]. Cannabis is consumed by various routes, with the most common route smoking Baggio et al. [3]. Inhalation by smoking or vaporization releases maximal levels of THC into blood within minutes, peaking at 15-30 minutes, and decreasing within 2-3 hours. Even with a fixed dose of THC in a cannabis cigarette, THC pharmacokinetics and effects vary as a function of the weight of a cannabis cigarette its preparation, the concentration of other cannabinoids, the rate of inhalation, depth and duration of puffs, volume inhaled, extent of breath-holding, vital capacity, escaped smoke and dose titration Azorlosa et al. [4]; Azorlosa et al. [5]. The components of cannabis smoke become more concentrated and stronger towards the end with each puff Tashkin et al. [6]. So the smoking of fewer cannabis cigarettes down to a shorter butt length could mean taking in a greater number of smoke components than smoking the same amount of cannabis in more cigarettes smoked to a longer butt length British Lung Foundation [7]. In humans smoking one or more cannabis cigarettes, THC levels in peripheral blood exceeded the range of 5 to 250ng/ml, while intravenous administration of 10mg/kg THC resulted in a blood level of 720ng/ml after 20 minutes Safarian et al. [8]. An extensive comparison of smoke (mainstream: smoke exhaled by a smoker and side stream: smoke generated from the end of a cigarette) generated by igniting cannabis and tobacco cigarettes, showed marked qualitative similarities in specific compounds (e.g. ammonia, carbon monoxide, hydrogen cyanide, among others), and also significant quantitative differences Moir et al. [9]. Blood cell production and release of anandamide may complicate measurement of endocannabinoids in blood. This complication arises from the observation that ex vivo blood samples have high rates of anandamide release and this may clearly confound analytical measurements Vogeser et al. [10] Cannabis smoking was identified in the determinants of myocardial infarction study as a risk factor for initiating a myocardial infarction, such that the risk was increased 4.8-fold in the 60min after its use Mittleman et al. [11]. The acute administration of cannabis being associated with an increased risk of myocardial infarction and the coronary artery risk developing in young adults trial Rodondi et al. [12]. Cannabis smoking is associated with cardiovascular effects including tachycardia and hypertension with orthostatic hypotension. The tachycardia clearly acts as a stressor, and smoking cannabis (when compared to placebo controls) has been shown provoke symptoms instable angina Aronow and Cassidy [13]. The present study tries to focus on whether cannabis abuse produces alterations in hematological parameters which leads to endorse health disorders among Kashmiri people.
Objective: The objective of the present study is to compare the blood test among cannabis abusers and control group to see the changes formed by cannabis abuse whether (higher or lower) in hematological indices to highlight the associated health and blood disorders.
Hypothesis: There will be significant differences in Hemoglobin, Hematocrit, RBC, MCV, MCH, MCHC, ROW-CV, Platelet, Leucocytes, Neutrophil, Lymphocytes, Monocytes, Eosionophills, Basophills, absolute Neutrophil, absolute Lymphocyte, absolute Monocytes, absolute Eisnophills, absolute Basophills and Glucose fasting levels between cannabis abusers and control group of Kashmiri youth.
Methods: A purposive sample of 300 male participant were taken into consideration for complete blood count test in which 150 were belong to cannabis abusers who smoke 10 or more joints per day from last 15 years and are admitted in drug deaddiction center and remaining 150 were belong to control group and the mean age of the sample were 30.34 years.
Tool Used: Complete blood count (CBC) was taken as a tool to analyze the hematological variations produced by cannabis abuse (Tables 1 & 2) and (Figure 1).
Results and Discussion
The result of the study showed that two groups significantly differed on Hemoglobin, Hematocrit, RBC count, platelet count, total Leucocyte count, Neutrophils, Lymphocytes, Monocytes, Eosionophills, Basophil, absolute Neutrophil count, absolute Lymphocytes count, absolute Monocyte count, absolute Eosionophil count, absolute Basophills and glucose fasting. While on the other hand MCV, MCH, MCHC and RDW-CV showed nonsignificant differences between cannabis abusers and control group on blood count test. Cannabis abusers showed lower scores in hemoglobin in complete blood count test (M=14.58) in comparison with control group (M=18.47). Chronic consumption of Cannabis showed that the RBC increased dose dependently with the packed cell volume not showing any considerable difference among the groups. Early studies in line indicated that there was increased hemoglobin content which agrees with the findings of Karimi et al. 13] and this may indicate that the consumption of high dose of cannabis sativa may improve oxygen carrying capacity in blood. However, the mechanism of action is not known. In context of hematocrit control group showed higher scores (M=49.76) in accord with cannabis abusers (M=43.56). In the present study cannabis abusers showed lower RBC count (M=3.23) in evaluation with control group (M=8.54). The tetrahydrocannabinol THC has long term significant toxicological implications such as bone marrow suppression and disturbs the maturation of monocytes as well as erythrocytes (Karimi et al, 2007). Cannabis abusers showed lower scores in MCV (M=79.41) in accord with control group (M=80.67). In context of MCH cannabis abusers showed lower scores (M= 31.92) in contrast with control group (M=30.41). Cannabis abusers showed lower score in MCHC (M=34.37) in standpoint with control group (M= 33.89). In the milieu of RDWCV the cannabis abusers showed lowers scores (M=13.33) in comparison with control group (14.16). The early research in line showed significant differences in the hematological parameters between the cannabis smokers (Test) and non-smoker (control) subjects. Faster pulse rate and lower body temperatures were seen among test subjects as compared to control. The values observed for total white blood cell (TWBC), ESR and RBC were lower in test subject (smokers) than the control (non-smokers), while the values observed for ESR, Hb, and RBC were relatively close. The mean values observed for PCV, TWBC and Hb were markedly lower in test subject than in control and could be indicative of reduced percentage of blood in the cell Nwaichi and Omorodion [14]. It is plausible that treatment with high dose of Cannabis sativa extract had a microcytic effect, while treatment with low dose of Cannabis sativa had a normocytic effect. Another index for diagnosing anemia is mean corpuscular hemoglobin (MCH) and mean corpuscular hemoglobin concentration (MCHC) Archibong et al. [15]. MCH showed no differences between the control and cannabis sativa treated groups. The MCHC also did not show any difference between control and low dose groups, but was significantly raised in high dose group. However low MCHC is an indicator of hypochromia in early iron deficiency, and MCH level decreases as the hypochromia develops. It is therefore plausible that cannabis sativa contains Hb production enhancing factors. This may therefore prevent the likelihood of hypochromia in the Cannabis sativa treated rats Rose and Bentley [16].
Cannabis abusers showed higher scores in platelet count (M= 92.15) in accord with control group (M=76.56). Literature revealed that the cannabis dose dependent increase in platelet count. This is contrary to the report by Oseni et al. [17] reported a decrease in platelets count in human subjects. The disparity in results could be due to difference in species of animals used, duration of test as well as quality and quantity of Cannabis sativa used. This result however agrees with the findings of Maccarrone et al. [18]; Gautheir [19] who both found that Cannabis sativa consumption leads to platelet activation. The increased platelet count is probably a contributory factor in the thrombogenic potential and its implication in cardiovascular shock and myocardial infarction Mean corpuscular volume (MCV) which is the average volume of a single RBC showed a significant reduction in the high dose group compared to control and low dose groups. In patients with anaemia, MCV measurement allows for classification as microcytic (MCV below normal range), normocytic (MCV within normal range) or macrocytic (MCV above normal range) Randal et al. [20] In the perspective of total Leucocyte count cannabis abusers showed lower scores (M=7.54) in comparison with control group (M=10.32). In the context of Neutrophils the cannabis abusers showed lower scores (M=69.32) in perspective with control group (M=75.24). In the context of Lymphocytes the control group showed higher scores (M=19.33) in accord with cannabis abusers (M=13.33). The exposure to cannabis sativa using different routes can result in different effects. The total white cells count decreased significantly in all treated rats and that was due to the significant reduction of the neutrophils and lymphocytes percentages. The reduction of the neutrophils in the addicted smokers was not significant but with significant increase in the lymphocytes count Mukhtar & Elbagir [21]. The activation of CB2, cannabinoid 2 receptor reduced ischemic injury this action involved the reduction of the number of neutrophils in the ischemic brain of experimental mice Murikinati et al. [22].
In the back ground of Monocytes the cannabis abusers showed lower scores (M=5.32) in relation with control group (M=9.43). In the context of Eosionophills the cannabis abusers showed lower scores (M=3.92) in perspective of control group (M=7.32). In the frame work of Basophil the control group showed higher scores (M=6.43) in deal with cannabis abusers (M=2.77). Early research in line showed resembles with present study and indicated that there was a decrease in total white blood cells count in the group fed low and high doses of cannabis sativa when compared with control. This may be one of the reasons Cannabis sativa is used in anti-inflammatory conditions (Russo, 2001). In the context of absolute Neutrophil count the cannabis abusers showed lower scores (M=5.22) in relation with control group (M=8.98). In the back ground of absolute Lymphocytes count the cannabis showed lower scores (M=2.56) in accord with control group). In the line of absolute Monocytes count the cannabis abusers showed lower scores (M=2.38) in the harmony with control group (M=6.78). In the perspective of absolute Eosionophil count the cannabis abusers showed lower scores (M=1.17) in the milieu of control group (M=4.77). In the frame work of absolute Basophil the cannabis abusers showed lower scores (M=2.03) in reference with control group (M=7.01). Earlier research indicated that cannabis sativa may lead to thromboembolism, production of immature monocytes, reduced white blood cell count and by implication reduced body defense mechanism, and it may improve RBC count with no concomitant increase in PCV but with improved Hb which is also shown in the high MCHC at high volume content and therefore an improved oxygen carrying capacity. It may therefore be recommended that individuals with anemia or immune complications should not use Cannabis sativa in their food preparation on regular basis Obembe et al. [23]. In the glucose fasting parameter of complete blood count cannabis abusers showed higher scores (M=76.53) in concurrence with control group (M=59.71). Literature revealed that there were signifi¬cant increases in fasting blood glucose and triglycerides and a decrease in high-density lipoprotein cholesterol for the cannabis negative group, with no significant changes in the cannabis positive group. Rates of metabolic syn¬drome did not differ significantly between groups Scheffler et al. [24].
Conclusion
Cannabis abuse fabricate changes in hematological indices such as in Hemoglobin, Hematocrit, RBC, MCV, MCH, MCHC, RDW-CV, Platelets, Leucocytes, Neutrophils, Lymphocytes, Monocytes, Eosionophil, basophil, absolute Neutrophils, absolute Lymphocytes, absolute Monocytes, absolute Eosionophills and Glucose fasting. These changes cause bone marrow suppression, thromboembolism, and hypochromia neutropenia, neutrophilic, leukocytosis, lymphocytopenia, lemphocytic leukocytosis, hypothyroidism, cushing syndrome, sepsis, asthama, allergic rhinitis, attropic dermatitis, leukemia, hereditary sperocytosis, hemolatic anemia and reduced body defense mechanism [25,26].
Acknowledgement
The author appreciates all those who participated in the study and helped to facilitate the research process.
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