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Dive into the research topics where Albert Akpalu is active.

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Featured researches published by Albert Akpalu.


Brain | 2014

The modern pre-levodopa era of Parkinson’s disease: insights into motor complications from sub-Saharan Africa

Roberto Cilia; Albert Akpalu; Fred Stephen Sarfo; Momodou Cham; Marianna Amboni; Emanuele Cereda; Margherita Fabbri; Patrick Adjei; John Akassi; Alba Bonetti; Gianni Pezzoli

Delaying the initiation of levodopa has been proposed to reduce the risk of motor complications in Parkinson’s disease. In a 4-year multicentre study in Ghana, Cilia et al. find that motor fluctuations and dyskinesias are predicted by disease duration and levodopa dose, but not by the duration of levodopa therapy.


Cardiovascular Journal of Africa | 2015

The burden of stroke in Africa: a glance at the present and a glimpse into the future.

M.O. Owolabi; Sally N Akarolo-Anthony; Ro Akinyemi; Donna K. Arnett; Mulugeta Gebregziabher; Carolyn Jenkins; H. Tiwari; O. Arulogun; Albert Akpalu; Fred Stephen Sarfo; Reginald Obiako; Lukman Owolabi; Kwamena W. Sagoe; S. Melikam; Abiodun M. Adeoye; Daniel T. Lackland; Bruce Ovbiagele

Summary Objective Information on the current burden of stroke in Africa is limited. The aim of this review was to comprehensively examine the current and projected burden of stroke in Africa. Methods We systematically reviewed the available literature (PubMed and AJOL) from January 1960 and June 2014 on stroke in Africa. Percentage change in age-adjusted stroke incidence, mortality and disability-adjusted life years (DALYs) for African countries between 1990 and 2010 were calculated from the Global Burden of Diseases (GBD) model-derived figures. Results Community-based studies revealed an age-standardised annual stroke incidence rate of up to 316 per 100 000 population, and age-standardised prevalence rates of up to 981 per 100 000. Model-based estimates showed significant mean increases in age-standardised stroke incidence. The peculiar factors responsible for the substantial disparities in incidence velocity, ischaemic stroke proportion, mean age and case fatality compared to high-income countries remain unknown. Conclusions While the available study data and evidence are limited, the burden of stroke in Africa appears to be increasing.


Epilepsia | 2007

Differential Cellular Gene Expression in Ganglioglioma

Uzma Samadani; Alexander R. Judkins; Albert Akpalu; Eleonora Aronica; Peter B. Crino

Summary:  Purpose: Gangliogliomas (GGs) are neuronal‐glial tumors highly associated with epilepsy. We hypothesized that the expression of select gene families including neurotransmitter receptor subunits and growth factors would be distinct in neurons and astrocytes within GG compared with adjacent cortex and that these changes would yield insights into seizure onset and lesion formation.


Epilepsia | 2014

Clinical features, proximate causes, and consequences of active convulsive epilepsy in Africa.

Symon M. Kariuki; William Matuja; Albert Akpalu; Angelina Kakooza-Mwesige; Martin Chabi; Ryan G. Wagner; Myles Connor; Eddie Chengo; Anthony K. Ngugi; Rachael Odhiambo; Christian Bottomley; Steven White; Josemir W. Sander; Charles R. Newton

Epilepsy is common in sub‐Saharan Africa (SSA), but the clinical features and consequences are poorly characterized. Most studies are hospital‐based, and few studies have compared different ecological sites in SSA. We described active convulsive epilepsy (ACE) identified in cross‐sectional community‐based surveys in SSA, to understand the proximate causes, features, and consequences.


Neuroepidemiology | 2015

Phenotyping Stroke in Sub-Saharan Africa: Stroke Investigative Research and Education Network (SIREN) Phenomics Protocol

Albert Akpalu; Fred Stephen Sarfo; Bruce Ovbiagele; Rufus Akinyemi; Mulugeta Gebregziabher; Reginald Obiako; Lukman Owolabi; Kwamena W. Sagoe; Carolyn Jenkins; Oyedunni Arulogun; Sheila Adamu; Lambert Tetteh Appiah; Martin A. Adadey; Francis Agyekum; Joseph A. Quansah; Yaw Mensah; Abiodun M. Adeoye; Arti Singh; Aridegbe Tosin; Osimhiarherhuo Ohifemen; Abubabkar A. Sani; Eric Tabi-Ajayi; Ibinaiye Phillip; Suleiman Isah; Nasir Tabari; Aliyu Mande; Atinuke Agunloye; Godwin Ogbole; Joshua O. Akinyemi; Onoja Akpa

Background: As the second leading cause of death and the leading cause of adult-onset disability, stroke is a major public health concern particularly pertinent in Sub-Saharan Africa (SSA), where nearly 80% of all global stroke mortalities occur, and stroke burden is projected to increase in the coming decades. However, traditional and emerging risk factors for stroke in SSA have not been well characterized, thus limiting efforts at curbing its devastating toll. The Stroke Investigative Research and Education Network (SIREN) project is aimed at comprehensively evaluating the key environmental and genomic risk factors for stroke (and its subtypes) in SSA while simultaneously building capacities in phenomics, biobanking, genomics, biostatistics, and bioinformatics for brain research. Methods: SIREN is a transnational, multicentre, hospital and community-based study involving 3,000 cases and 3,000 controls recruited from 8 sites in Ghana and Nigeria. Cases will be hospital-based patients with first stroke within 10 days of onset in whom neurovascular imaging will be performed. Etiological and topographical stroke subtypes will be documented for all cases. Controls will be hospital- and community-based participants, matched to cases on the basis of gender, ethnicity, and age (±5 years). Information will be collected on known and proposed emerging risk factors for stroke. Study Significance: SIREN is the largest study of stroke in Africa to date. It is anticipated that it will shed light on the phenotypic characteristics and risk factors of stroke and ultimately provide evidence base for strategic interventions to curtail the burgeoning burden of stroke on the sub-continent.


eNeurologicalSci | 2016

Profile of neurological disorders in an adult neurology clinic in Kumasi, Ghana

Fred Stephen Sarfo; John Akassi; Elizabeth Badu; Aham Okorozo; Bruce Ovbiagele; Albert Akpalu

Background Although the burden of neurological disorders is highest among populations in developing countries there is a dearth of data on the clinical spectrum of these disorders. Objective To profile the frequency of neurologic disorders and basic demographic data in an adult neurology out-patient service commissioned in 2011 in Kumasi, Ghana. Methods The study was conducted at the neurology clinic of the Komfo Anokye Teaching Hospital in Kumasi, Ghana. Over a three year period, all medical records of patients enrolled at the out-patient neurology clinic was reviewed by a neurologist and neurological diagnoses classified according to ICD-10. Results 1812 adults enrolled for care in the neurology out-patient service between 2011 and 2013. This comprised of 882 males and 930 females (male: female ratio of 1.0: 1.1) with an overall median age of 54 (IQR, 39–69) years. The commonest primary neurological disorders seen were strokes, epilepsy and seizure disorders, and movement disorders at frequencies of 57.1%, 19.8%, and 8.2% respectively. Conclusions Cerebrovascular diseases, epilepsy and movement disorders were among the commonest neurological disorders and the major contributors to neurologic morbidity among Ghanaians in an urban neurology clinic.


Cardiovascular Journal of Africa | 2015

Stroke genomics in people of African ancestry: charting new paths.

Ro Akinyemi; Bruce Ovbiagele; Albert Akpalu; Carolyn Jenkins; Kwamena W. Sagoe; Lukman Owolabi; Fred Stephen Sarfo; Reginald Obiako; M. Gebreziabher; Ezinne Melikam; S. Warth; Oyedunni Arulogun; Daniel T. Lackland; Adesola Ogunniyi; Hemant K. Tiwari; Raj N. Kalaria; Donna K. Arnett; Mayowa Owolabi

Abstract One in six people worldwide will experience a stroke in his/her lifetime. While people in Africa carry a disproportionately higher burden of poor stroke outcomes, compared to the rest of the world, the exact contribution of genomic factors to this disparity is unknown. Despite noteworthy research into stroke genomics, studies exploring the genetic contribution to stroke among populations of African ancestry in the United States are few. Furthermore, genomics data in populations living in Africa are lacking. The wide genomic variation of African populations offers a unique opportunity to identify genomic variants with causal relationships to stroke across different ethnic groups. The Stroke Investigative Research and Educational Network (SIREN), a component of the Human Health and Heredity in Africa (H3Africa) Consortium, aims to explore genomic and environmental risk factors for stroke in populations of African ancestry in West Africa and the United States. In this article, we review the literature on the genomics of stroke with particular emphasis on populations of African origin.


Stroke | 2016

Multilingual Validation of the Questionnaire for Verifying Stroke-Free Status in West Africa

Fred Stephen Sarfo; Mulugeta Gebregziabher; Bruce Ovbiagele; Rufus Akinyemi; Lukman Owolabi; Reginald Obiako; Onoja Akpa; Kevin S. Armstrong; Albert Akpalu; Sheila Adamu; Vida Obese; Nana Boa-Antwi; Lambert Tetteh Appiah; Oyedunni Arulogun; Yaw Mensah; Abiodun M. Adeoye; Aridegbe Tosin; Osimhiarherhuo Adeleye; Eric Tabi-Ajayi; Ibinaiye Phillip; Abubakar Sani; Suleiman Isah; Nasir Tabari; Aliyu Mande; Atinuke Agunloye; Godwin Ogbole; Joshua O. Akinyemi; Ruth Laryea; Sylvia Melikam; Ezinne Uvere

Background and Purpose— The Questionnaire for Verifying Stroke-Free Status (QVSFS), a method for verifying stroke-free status in participants of clinical, epidemiological, and genetic studies, has not been validated in low-income settings where populations have limited knowledge of stroke symptoms. We aimed to validate QVSFS in 3 languages, Yoruba, Hausa and Akan, for ascertainment of stroke-free status of control subjects enrolled in an on-going stroke epidemiological study in West Africa. Methods— Data were collected using a cross-sectional study design where 384 participants were consecutively recruited from neurology and general medicine clinics of 5 tertiary referral hospitals in Nigeria and Ghana. Ascertainment of stroke status was by neurologists using structured neurological examination, review of case records, and neuroimaging (gold standard). Relative performance of QVSFS without and with pictures of stroke symptoms (pictograms) was assessed using sensitivity, specificity, positive predictive value, and negative predictive value. Results— The overall median age of the study participants was 54 years and 48.4% were males. Of 165 stroke cases identified by gold standard, 98% were determined to have had stroke, whereas of 219 without stroke 87% were determined to be stroke-free by QVSFS. Negative predictive value of the QVSFS across the 3 languages was 0.97 (range, 0.93–1.00), sensitivity, specificity, and positive predictive value were 0.98, 0.82, and 0.80, respectively. Agreement between the questionnaire with and without the pictogram was excellent/strong with Cohen k=0.92. Conclusions— QVSFS is a valid tool for verifying stroke-free status across culturally diverse populations in West Africa.


The Pan African medical journal | 2015

Prevalence and risk factors for Active Convulsive Epilepsy in Kintampo, Ghana

Kenneth Ayuurebobi Ae-Ngibise; Bright Akpalu; Anthony K. Ngugi; Albert Akpalu; Francis Agbokey; Patrick Adjei; Damien Punguyire; Christian Bottomley; Charles R. Newton; Seth Owusu-Agyei

Introduction Epilepsy is common in sub-Saharan Africa, but there is little data in West Africa, to develop public health measures for epilepsy in this region. Methods We conducted a three-stage cross-sectional survey to determine the prevalence and risk factors for active convulsive epilepsy (ACE), and estimated the treatment gap in Kintampo situated in the middle of Ghana. Results 249 people with ACE were identified in a study population of 113,796 individuals. After adjusting for attrition and the sensitivity of the screening method, the prevalence of ACE was 10.1/1000 (95% Confidence Interval (95%CI) 9.5-10.7). In children aged <18 years, risk factors for ACE were: family history of seizures (OR=3.31; 95%CI: 1.83-5.96), abnormal delivery (OR=2.99; 95%CI: 1.07-8.34), problems after birth (OR=3.51; 95%CI: 1.02-12.06), and exposure to Onchocerca volvulus (OR=2.32; 95%CI: 1.12-4.78). In adults, a family history of seizures (OR=1.83; 95%CI: 1.05-3.20), never attended school (OR=11.68; 95%CI: 4.80-28.40), cassava consumption (OR=3.92; 95%CI: 1.14-13.54), pork consumption (OR=1.68; 95%CI: 1.09-2.58), history of snoring at least 3 nights per week (OR=3.40: 95%CI: 1.56-7.41), exposure to Toxoplasma gondii (OR=1.99; 95%CI: 1.15-3.45) and Onchocerca volvulus (OR=2.09: 95%CI: 1.29-3.40) were significant risk factors for the development of ACE. The self-reported treatment gap was 86.9% (95%CI: 83.5%-90.3%). Conclusion ACE is common within the middle belt of Ghana and could be reduced with improved obstetric care and prevention of parasite infestations such as Onchocerca volvulus and Toxoplasma gondii.


Nutrition | 2013

Nutritional status and dietary habits in Parkinson's disease patients in Ghana.

Michela Barichella; Albert Akpalu; Momodou Cham; Giulia Privitera; Erica Cassani; Emanuele Cereda; Laura Iorio; Roberto Cilia; Alba Bonetti; Gianni Pezzoli

OBJECTIVE Dietary treatment is important for the management of Parkinsons disease (PD). Our objective was to describe the dietary habits and assess the nutritional status of Ghanaian patients with PD. This study is part of a larger project, for which Ghana has been selected as a pilot country. METHODS Fifty-five Ghanaian patients with PD and 12 healthy Ghanaian controls were recruited. We assessed nutritional status, investigated dietary habits, and assessed the prevalence of the nutritional complications of PD (e.g., constipation and dysphagia). RESULTS The mean daily caloric intake was about 1200 kcal/d in patients with PD and in controls. The typical diet was based on semisolid foods, usually vegetable soups accompanied by cereal flour or root starch or sometimes chicken or fish. The intake of milk and its derivatives was low. The prevalences of constipation and dysphagia in patients with PD were 49% and 21%, respectively. CONCLUSION This study has yielded information that could be useful for the study of the management of PD and for the assessment of response to therapy.

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Fred Stephen Sarfo

Komfo Anokye Teaching Hospital

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Bruce Ovbiagele

University of South Carolina

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Carolyn Jenkins

Medical University of South Carolina

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