Abnormal coagulation profile in people living with HIV-AIDS on combined Antiretroviral Therapy: findings from a case-control study in the Ho municipality, Ghana

Abnormal coagulation profile in people living with HIV-AIDS on combined Antiretroviral Therapy: findings from a case-control study in the Ho municipality, Ghana

Richard Kobina Dadzie Ephraim¹, James Elikem Ahadzie¹, Patrick Adu^1,&, Joseph Boachie¹, Hope Agbodzakey¹, Prince Adoba¹, Obed Cudjoe¹

 

¹Department of Medical Laboratory Technology, School of Allied Health Sciences, College of Health and Allied Sciences (COHAS), University of Cape Coast, Ghana

 

 

^&Corresponding author
Patrick Adu, Department of Medical Laboratory Technology, School of Allied Health Sciences, College of Health and Allied Sciences (COHAS), University of Cape Coast, Ghana

 

 

 

 

Human immunodeficiency virus (HIV) infection/acquired immunodeficiency syndrome (AIDS), is a global pandemic caused by infection with human immunodeficiency virus [1, 2]. As of 2016, approximately 36.7 million people were living with HIV globally [3]. Ghana's HIV prevalence rate currently stands at 2.4% according to the Ghana Aids Commission [4]. The main immunological complication of HIV infection is cellular CD4+ T-lymphocyte depletion, for which various causal mechanisms have been proposed. Among these are HIV-induced cytolysis; dysregulation of cytokines; cytotoxic T lymphocyte responses and HIV-induced autoimmune reactions [5]. The introduction of combined antiretroviral therapy (cART) for treatment of HIV infection has generally been accepted as the gold standard in the management of HIV patients [6]. Since the advent of effective antiretroviral therapy (ART) for HIV, there has been a substantial decrease in deaths related to HIV/AIDS [7] as well as non-AIDS associated events. Different anti-retroviral agents target different steps in HIV replication including glycoprotein components 120 and 41 as well as enzymes involved in HIV replication [8]. Recently, Omoregie et al., found that HIV patients with CD4 count < 200 cell/µL had higher PT and APTT values; although only PT correlated with CD4 counts [9]. They opined that the progression of the HIV infection consequently causes endothelial dysfunction and liver damage that might result in severe clotting impairment [9]. Another study also found that 34.88% of the sampled HIV infected individuals had deranged partial thromboplastin time activated with kaolin (PTTK), with 9 out of 10 of those with the deranged PTTK also demonstrating thrombotic disorders as a result of the presence of circulating anticoagulant [10]. However, another study by Dikshit et al., found no case of coagulation abnormalities in the HIV patients studied [11] suggesting the need for further studies to clarify the impact of HIV infection as well as cART therapy on the coagulation profile of these patients. In this study we sought to compare the coagulation profiles of HIV persons on cART to that of cART naïve HIV patients to assess the coagulation profiles and how cART therapy might impact these factors.

 

 

Study setting/study design/participants: this hospital-based case-control study was conducted from January to April 2014 at the Volta Regional Hospital in Ho, the capital of the Volta Region of Ghana. Confirmed PLWHA (110), comprising 65 on cART and 45 cART naive patients visiting the ART clinic were recruited onto the study. The antiretroviral drugs being used by the participants were various combinations (CB) of Zidovudine (AZT) + Lamivudine (LAM) + Efavirenz (EFV) as CB1; AZT + LAM + Nevirapine (NEV) as CB2; AZT + NEV + EFV as CB3. However, participants with myeloproliferative disorders, liver diseases, those on other drugs apart from cART and those on anticoagulant therapy where excluded. Other clinical and demographic information was collected using questionnaire. Ethical approval was obtained from the University of Cape Coast Institutional Review Board (UCCIRB) and the Ethical Committee of the hospital before commencement of the study. Written informed consent was sought from the participants before collecting their data and samples.

 

Blood Sample Collection and processing: five (5) ml blood was collected from the study participants for coagulation studies (PT, APTT, INR) (citrated tubes at blood to anticoagulant ratio of 9:1) and full blood count (FBC) (EDTA anticoagulated tubes). The blood for coagulation studies was centrifuged at 1500 rpm for 3-5 minutes and the plasma separated.

 

PT, APTT, FBC estimation: the plasma was used to estimate prothrombin time (PT), activated partial thromboplastin time (APTT) using standard operating procedures as previously described [12] EDTA anti-coagulated blood was used to estimate the WBC, lymphocyte count, platelet count by using the automated Sysmex X-500i haematology analyzer (Sysmex Corporation, Japan). The WBC stratification was based on previously recommended reference range in the literature [13].

 

Statistical analysis: the data were entered into Microsoft excel and analyzed using IBM Statistical Package for Social Sciences (SPSS) statistics for windows, version 21.0 (Armonk NY; IBM Corporation). Data were expressed as means and percentages for different variables. Comparison between variables was done using Chi-square test. One-way ANOVA was also used to compare means of scores of more than two groups. Continuous variables were analyzed using unpaired student's T -test for variation among HIV naïve individuals and those on cART. Statistical significance level was set at P<0.05.

 

 

Table 1 summarizes the general characteristics of the study participants. The PT (13.83 ± 2.05 vs 17.24 ± 4.24), and INR (1.2 ± 0.2 vs 1.44 ± 0.4) were significantly reduced in Patients on cART compared to the cART naïve patients (p<0.001, both in patients on cART). Though the APTT was also lower in the patients on cART compared to cART naïve patients, this did not reach statistical significance (p=0.081). However, although platelet counts were higher in patients on cART compared to cART naïve patients, the difference did not reach statistical significance (p=0.402). In addition, WBC counts were reduced in patients on cART compared to cART naïve patients. Table 2 shows the coagulation profile of the study participants. Majority of the participants on cART had a normal PT (10-15 sec) compared to the cART naïve participants (75.4% v 33.3%; P< 0.001). Moreover, majority of the cART naïve participants had prolonged PT (> 15 sec) than those on cART (66.7% v 23.1%; P< 0.001) suggesting a potential role of cART in restoring the PT. In addition, a higher proportion of cART participants (21.5%) had estimated APTT within the reference range, compared to 13.3% cART naïve participants. Interestingly, whereas 78.5% of cART participants had prolonged APTT (APTT >45 seconds), 86.7% of cART naïve participants had prolonged APTT. The effects of different cART regimen on PT, APTT, platelet and WBC counts were also investigated (Table 3). Participants on drug combination 2 (AZT+LAM+NEV) had a significantly higher mean PT and INR when compared to those on drug combinations 3 (AZT+NEV+EFV) and 1 (AZT+LAM+EFV) respectively (p=0.020, one-way ANOVA). Comparatively, CB2 appeared less able to restore PT (40.7% had PT>15 seconds) in contrast to those on CB1 (7.4%) or CB3 (18.2%) therapy (p=0.013; one-way ANOVA). With regards to the APTT, participants on CB3 had lower mean APTT compared to CB1 or CB2 {47.55 versus 56.81 (CB1) or 56.85 (CB2); p=0.058}. More importantly, a significantly greater proportion of participants on CD3 had APTT in the reference range when compared to CB1 and CB3 (63.6% versus 11.1% & 14.8% respectively; p <0.001). Moreover, whereas only 36.4% of participants on CB3 had prolonged APTT (APTT >45 seconds), significantly higher proportions of participants on CB1 (88.9%) and CB2 (85.2%) had prolonged APTT (p< 0.001). In addition, whereas a lower proportion of participants on CB3 had <4x10³/mm³ compared to CB1 and CB2 {27.3% versus 63% (CB1), or 59.3% (CB2); p = 0.116}, a higher proportion of participants on CB3 had WBC of 4-10x103/mm³ when compared to CB1 or CB2 {72.7% versus 37% (CB1), or 37% (CB2); p = 0.093}.

 

 

In this study we determined the effect of cART on the coagulation profile of HIV/AIDS patients. Our results showed that participants on cART had lower mean PT and APTT, but higher platelet counts when compared to their cART naïve HIV patients. In addition, whereas the PT and APTT of cART participants were generally within the reference range, these parameters for the cART naïve participants were generally higher than the upper limit of the reference range suggesting a potential role of cART to restore and/or correct these coagulation factor derangements. Recently, Omokaro et al., reported that HIV seropositive patients have higher APTT and PT than HIV seronegative persons [9]. In spite of the increased APTT and PT, they further stated that only PT positively correlated with the CD4 counts in HIV seropositive individuals and suggested endothelial dysfunction as underlying defect in the prolonged APTT and PT in these patients. Although our study did not assess the functional capacity of the liver in these participants, it could be argued that the improved PT and APTT reported herein amongst the participants on cART could have been the consequence of cART improving the hepatic functional ability to synthesize some coagulation factors that are indirectly assessed through the PT and APTT assay.

 

Interestingly, this study also showed that the type of cART regimen or drug combination has significant effect on the restoration of normal coagulation profile in these patients. Patients on cART combination 3 [ Zidovudine (AZT) + Nevirapine (NEV) + Efavirenz (EFV)] appeared to have a more favourable coagulation profile as these participants had lower mean APTT and PT compared to those on cART combination 1 [AZT + Lamivudine (LAM) + EFV] or cART combination 2 [AZT+LAM+ Nevirapine (NEV)]. In addition, a higher proportion of participants on cART combination 3 had their APTT and PT restored to the reference range values when compared to CB1 or CB2. This is an interesting observation considering that it is generally proposed that two nucleoside reverse transcriptase inhibitors should form the backbone of cART therapy [14] for optimal response. cART combination 3 however contained only one nucleoside reverse transcriptase inhibitor (AZT) and two non-nucleoside reverse transcriptase inhibitors (NEV + EFV). This is also against the backdrop of previous report that suggested an association of hepatotoxicity with nevirapine treatment [15]. It will be interesting to investigate the variability in the responses of different races or population groups to the various cART combinations. Moreover, whereas cART naïve HIV/AIDS patients had higher mean total WBC counts compared to cART treated HIV patients, CB3 was more effective in raising the WBC counts when compared to CB1 or CB2. As high as 72.7% of participants on cART CB3 had their WBC counts restored to the reference range when compared to 37% participants on either cART CB1 or CB2. Our findings agree with a previous report by Omoregie et al who showed that HIV-positive patients have significantly lower CD4 and platelet counts than HIV-negative subjects [9]. We propose that the increased WBC counts in participants on cART in this study might be due to a cART being able to restore bone marrow haematopoietic activity [16]. Our study, however, had a few limitations. As malnutrition has been shown to be a major factor in the HIV/AIDS disease burden in worldwide [17], it is reasonable to suppose that the nutritional status of the patients investigated might have had effect on the extent to which cART impacted the coagulation profile of these patients. We did not however, investigate effects of the indigenous dietary inclinations of the participants' vis-à-vis cART combination and coagulation profile. More so, this study did not investigate the duration of cART therapy on the coagulation parameters.

 

 

Findings from this study suggest that, these type of cART regimen could affect the coagulation and other haematopoietic profiles in PLWHA. Moreover, Zidovudine + Nevirapine + Efavirenz combined therapy had the most beneficial effects in correcting for PT, APTT and total WBC counts in the population studied. Future studies addressing the associations between local dietary choices, cART combination, and coagulation profiles of PLWHA would likely yield interesting findings.

 

 

The authors declare no competing interests.

 

 

RKDE, PA, JB and JEA conceived of the study and participated in its design and coordination. RKDE, PA and JEA were involved in the recruitment of participants, data collection and analysis. RKDE, PA and OC drafted the manuscript. HA, OC and PA provided analytic and statistical support. All authors read and approved the final manuscript.

 

 

Our special appreciation is extended to the staff of the HIV/AIDS clinic and the laboratory personnel of the Volta Regional Hospital for their immeasurable contribution in making this work a success.

 

 

Table 1: general characteristics of study participants

Table 2: coagulation profile of study participants

Table 3: coagulation profile of study participants on cART stratified by the type of cART combination

 

 

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