Main Article Content
Abstract
ABSTRACT
Introduction. Several drugs of different chemical classes are used in the treatment of hypertension. Some of these drugs may induce liver injury. This study aimed at assessing the relationship between antihypertensive drugs and liver enzymes among hypertensive patients in Buea Regional Hospital. Methodology. A cross sectional hospital-based study was carried out from the month of February to May 2022. A total of 75 consenting hypertensive patients aged 21-60 years old were selected in a convenient manner. Socio-demographic data were obtained using a structured questionnaire while clinical data was obtained from medical records. Serum levels of liver enzymes were measured using a spectrophotometer based on kinetic methods. Data obtained was analysed using descriptive statistics, a Fisher’s exact test was used to test for association where appropriate and a P-value <0.05 was considered statistically significant. Results. Of the 75 participants enrolled y, 54(72%) were females while 21(28%) were males. Only 34.7% of the participants had their blood pressure controlled (BP <140/90mmHg). More than half of the study participants had normal serum levels for alanine aminotransferase (ALT), aspartate aminotransferase (AST) and for alkaline phosphatase (ALP): 92%, 64% and 90% respectively. Fisher’s test revealed that ALT and ALP showed a significant association with the side effects of the participants (p < 0.05 and p < 0.001, respectively). ALP was significant with the type of antihypertensive drug and complications of hypertension (p <0.005 and p <0.003, respectively). ALT was significantly associated with daily-dose frequency of the participants (p <0.05) and AST was significant with blood pressure (p <0.03). Conclusion. Most classes of antihypertensive drugs do not produce adverse effects in the liver based on liver enzymes measurement except for ALP which was positively associated with the type of antihypertensive drug particularly calcium channel blockers.
RÉSUMÉ
Introduction. Divers médicaments appartenant à différentes classes chimiques sont utilisés dans le traitement de l’hypertension artérielle. Certains de ces médicaments peuvent induire des atteintes hépatiques. Cette étude avait pour objectif d’évaluer la relation entre les médicaments antihypertenseurs et les enzymes hépatiques chez les patients hypertendus à l’Hôpital Régional de Buea. Méthodologie. Une étude transversale en milieu hospitalier a été menée de février à mai 2022. Un total de 75 patients hypertendus, âgés de 21 à 60 ans et ayant donné leur consentement éclairé, ont été recrutés de manière non probabiliste. Les données sociodémographiques ont été collectées à l’aide d’un questionnaire structuré, tandis que les données cliniques provenaient des dossiers médicaux. Les concentrations sériques des enzymes hépatiques ont été mesurées à l’aide d’un spectrophotomètre selon des méthodes cinétiques. Les données ont été analysées à l’aide de statistiques descriptives ; le test exact de Fisher a été utilisé pour rechercher une association lorsque cela était approprié, et une valeur de p < 0,05 a été considérée comme statistiquement significative. Résultats. Parmi les 75 participants, 54 (72 %) étaient des femmes et 21 (28 %) des hommes. Seuls 34,7 % des participants avaient une pression artérielle contrôlée (PA <140/90 mmHg). Plus de la moitié des participants présentaient des valeurs normales pour l’alanine aminotransférase (ALT), l’aspartate aminotransférase (AST) et la phosphatase alcaline (ALP), soit 92 %, 64 % et 90 % respectivement. Le test de Fisher a révélé une association significative entre l’ALT et l’ALP avec les effets secondaires rapportés par les participants (p < 0,05 et p < 0,001 respectivement). L’ALP était également significativement associée au type de médicament antihypertenseur utilisé et aux complications de l’hypertension (p < 0,005 et p < 0,003 respectivement). L’ALT était significativement liée à la fréquence quotidienne de prise médicamenteuse (p < 0,05) et l’AST était significativement associée à la pression artérielle (p < 0,03). Conclusion. La plupart des classes de médicaments antihypertenseurs n’induisent pas d’effets indésirables hépatiques selon les dosages enzymatiques, à l’exception de la phosphatase alcaline (ALP) qui a montré une association positive avec le type de médicament utilisé, en particulier les inhibiteurs des canaux calciques.
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References
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- 35. Carey RM, Whelton PK. Prevention, Detection, Evaluation, and Management of High Blood Pressure in Adults: Synopsis of the 2017 American College of Cardiology/American Heart Association Hypertension Guideline. Annals of Internal Medicine. 2018; 168(5): 351-8.
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- 38. Odili V, Oghagbon E, Ugwa N, Ochei U, Aghomo O. Adherence to International Guidelines in the Management of Hypertension in a Tertiary Hospital in Nigeria. Tropical Journal of Pharmaceutical Research. 2008; 7(2).
- 39. Preetha S. Estimation of liver function test in hypertension patients. Journal of Pharmaceutical Science Research. 2016; 8: 869.
References
1. American Heart Association. Obesity-induced hypertension: interaction of neurohumoraland renal mechanisms.Circular EconomyResearch. 2015; 116: 991-1006.
2. Lawoyin TO, Asuzu MC, Kaufman J, Rotimi C, Owoaje E, Johnson L, Cooper R.Prevalence of cardiovascular risk factors in an African, urban inner city community. West African Journal of Medicine 2002; 21(3): 208-11.
3. Bloch MJ. Worldwide prevalence of hypertension exceeds 1.3 billion. Journal of the American Society of Hypertension. 2016; 10(10): 753-4.
4. Zhou B, Perel P, Mensah GA, Ezzati M. Global epidemiology, health burden and effective interventions for elevated blood pressure and hypertension. Nature Reviews Cardiology. 2021; 10304: 932-933.
5. Guwatudde D, Nankya-Mutyoba J, Kalyesubula R, Laurence C, Adebamowo C, Ajayi I. The burden of hypertension in sub-Saharan Africa: a four-country cross sectional study. BioMed Central of Public Health. 2015; 15: 1211.
6. Kengne AP, Awah PK, Fezeu L, Mbanya JC. The burden of high blood pressure and related risk factors in urban sub-Saharan Africa: Evidences from Douala in Cameroon. Africa Health Science. 2007; 7(1): 38-44.
7. Kingue S, Ngoe CN, Menanga AP, Jingi AM, Noubiap JJN, Fesuh B. Prevalence and Risk Factors of Hypertension in Urban Areas of Cameroon: A Nationwide Population-Based Cross-Sectional Study. Journal of Clinical Hypertension.2015; 17(10): 819-24.
8. Jarari N,Rao N, Peela JR, Ellafi KA, Shakila S, Said AR. A review on prescribing patterns of antihypertensive drgs. Clinical Hypertension.2016; 22: 7.
9. Neal B,MacMahon S, Chapman N.Blood Pressure Lowering Treatment Trialists´ Collaboration, Effects of ACE inhibitors, calcium antagonists, and other blood-pressurelowering drgs: results of prospectively designed overviews of randomised trials, Blood Pressure Lowering Treatment Trialists´ Collaboration. Lancet London England journal. 2000; 356(9246): 1955-64.
10. Hansson L,Zanchetti A, George Carruthers S, Dahlöf B, Elmfeldt D, Julius S et al. Effects of intensive blood-pressure lowering and lowdose aspirin in patients with hypertension: principal results of the Hypertension Optimal Treatment (HOT) randomised trial HOT Study Group. Lancet. 1998; 351: 1755-62.
11. Cushma WC, Ford CE, Einhorn PT, Wright JT, Preston RA, Davis BR.Blood pressure control by drug group in the antihypertensive and lipid-lowering treatment to prevent heart attack trial (ALLHAT). Journal of Clinical Hypertension. Greenwich Conn. 2008; 10(10): 751-60.
12. Osterberg L, Blaschke T. Adherence to medication. New England Journal of Medicine.2005; 353: 487–97.
13. van Veen WA. Treatment adherence in hypertension: problems and research. Journal of Royal College of General Practitioners. 1980; (12): 22–5.
14. Burnier M,Wuerzner G, Struijker-Boudier H, Urquhart J.Measuring, analyzing, and managing drug adherence in resistant hypertension. Hypertension. 2013; 62: 218–25.
15. vanderLaan DM,Elders PJM, Boons CCLM, Beckeringh JJ, Nijpels G, Hugtenburg JG .Factors associated with antihypertensive medication nonadherence: a systematic review. Journal of Human Hypertension. 2017; 31: 687–94.
16. Corless JK, Middleton HM. Normal liver function: a basis for understanding hepatic disease. Archives of Internal Medicine.1983; 143: 2291–4.
17. Hanley AJG,Williams K, Festa A, Wagenknecht LE, D’Agostino RB, Kempf J. Elevations in markers of liver injury and risk of type 2 diabetes: the insulin resistance atherosclerosis study. Diabetes. 2004; 53: 2623–32.
18. Nkoke C, Noubiap JJ, Dzudie A, et al. Epidemiology of hypertensive crisis in Buea Regional Hospital, Cameroon. Journal of Clinical Hypertension. 2020; 22: 2105-2110.
19. World Health Organization. Isolated Systolic Hypertension. Hypertension journal. 2021
20. Schumann G, Klauke R. New IFCC reference procedures for the determination of catalytic activity concentrations of five enzymes in serum: preliminary upper reference limits obtained in hospitalized subjects. ClinicaChimicaActa. 2003; 327:69–79.
21. Tietz NW, Shuey DF. Reference intervals for alkaline phosphatase activity determined by the IFCC and AACC reference methods. Clinical Chemistry. 1986; 32: 1593–4.
22. Chobanian AV. National heart, lung, and blood institute; national high blood pressure education program coordinating committee. seventh report of the joint national committee on prevention, detection, evaluation, and treatment of high blood pressure. Hypertension. 2003; 42:1206–52.
23. Fryar CD, Ostchega Y, Hales CM, Zhang G and Kruszon-Moran D. Hypertension Prevalence and Control among Adults: United States, 2015-2016. National Center for Health Statistics. 2017; 289: 1-8.
24. Volpe M, Gallo G and Tocci G. Early and Fast Blood Pressure Control Important in Hypertension Management. International Journal of Cardiology. 2018; 254: 328-332.
25. Birditt KS, Newton N and Hope S. Implications of Marital/Partner Relationship: Quality and Perceived Stress for Blood Pressure among Adults. The Journals of Gerontology, Pyschological Sciences and Social Sciences. 2014; 69: 188-198.
26. Ramezankhani A, Azizi F and Hadaegh F. Association of Marital Status with Hypertension, Cardiovascular Disease: Long Term Follow-up Study. Public Library of Science. 2019; 14: e0215593.
27. Landi F, Calvani R, Picca A, Tosato M, Martone AM, Ortolani E, Fuga MT, Desideri G and Marzetti E. Body Mass Index is Strongly Associated with Hypertension: Results from the Longevity Check-up. Nutrients. 2018; 10: 1976.
28. Go AS, Mozaffarian D, Rogor VL. Heart disease and stroke statistics-2013 update: a report from the American Heart Association. Circulation 2013; 127: e6-e245.
29. Dzudie A, Kengne AP, Muna WF. Prevalence, awareness, treatment and control of hypertension in a self-selected sub-saharan African urban population: a cross-sectional study. British Medical Journal Open 2012: 2.
30. Maginga J, Guerrero M, Koh E. Hypertension control and its correlates among adults attending a Hypertension clinic in Tanzania. Journal of Clinical Hypertension 2016; 18: 207.
31. Sarganas G, Knopf H, Grams D, Neuhauser HK. Trends in Antihypertensive Medication Use and Blood Pressure Control Among Adults with Hypertension in Germany. American Journal of Hypertension. 2016; 29(1): 104-13.
32. Adebolu FA, Naidoo M. Blood pressure control amongst patients living with hypertension presenting to an urban district hospital outpatient clinic in Kwazulu-Natal. African Journal of Primary Health Care and Family Medicine. 2014; 6(1): E1-6.
33. Aronow, W. S. Treatment of hypertensive emergencies. Annals of Translational Medicine. 2017; 5(l1): s5.
34. Menanga A, Edie S, Nkoke C, Boombhi J, Musa AJ, Mfeukeu LK et al. Factors associated with blood pressure control amongst adults with hypertension in Yaoundé, Cameroon: a crosssectional study. Cardiovascular Diagnosis and Therapy. 2016; 6(5): 439-45.
35. Carey RM, Whelton PK. Prevention, Detection, Evaluation, and Management of High Blood Pressure in Adults: Synopsis of the 2017 American College of Cardiology/American Heart Association Hypertension Guideline. Annals of Internal Medicine. 2018; 168(5): 351-8.
36. Adejumo O, Okaka E, Iyawe I. Prescription pattern of antihypertensive medications and blood pressure control among hypertensive outpatients at the University of Benin Teaching Hospital in Benin City, Nigeria. Malawi Medical Journal Association. 2017; 29(2): 113-7.
37. Busari OA, Oluyonbo R, Fasae AJ, Gabriel OE, Ayodele LM, Agboola SM et al. Prescribing Pattern and Utilization of Antihypertensive Drgs and Blood Pressure Control in Adult Patients with Systemic Hypertension in a Rural Tertiary Hospital in Nigeria. American Journal of International Medicine. 2014; 2(6): 144.
38. Odili V, Oghagbon E, Ugwa N, Ochei U, Aghomo O. Adherence to International Guidelines in the Management of Hypertension in a Tertiary Hospital in Nigeria. Tropical Journal of Pharmaceutical Research. 2008; 7(2).
39. Preetha S. Estimation of liver function test in hypertension patients. Journal of Pharmaceutical Science Research. 2016; 8: 869.
