From: Epidemiology of neurodegenerative diseases in sub-Saharan Africa: a systematic review
Author, year of publication | Country | Setting | Design/period of study | Population characteristics | Diagnosis criteria | Prevalence | Profile of parkinsonism patients | Comments |
---|---|---|---|---|---|---|---|---|
Bower [10], 2005 | Ethiopia | Hospital | Cross-sectional 2003-2004 | 720 patients; 109 (15 · 1%) with movement disorders including 71 men; age 52 y. (13–80) | Not provided | 72/1,000 of all admissions (PD: 64/1,000) | N:52; PD:88% | Review of medical files/outpatient neurology clinic. |
Age (at onset): 57y (30–80) | ||||||||
Men: 75% | ||||||||
Akinyemi [11], 2008 | Nigeria | Hospital | Case–control 2005-2005 | 51 patients (men 37) with PD and 50 controls | UKPDS Brain Bank criteria | NA | N:51; PD: 100% | 22% patients with PD had cognitive dysfunction, with age at PD onset as sole predictor of cognitive dysfunction. |
Age (at onset): 70y (41–80) | ||||||||
Men:72% | ||||||||
Cosnett [12], 1988 | South Africa | Hospital | Cross-sectional 1979-1985 | 2638 patients | Clinical (Bradykinesia, rigidity, resting tremor and postural instability) | 5.3/1,000 | N:14; PD: 100% | Retrospective review of medical files/outpatient clinic |
Age: NA | Blacks: 1.5/1000 | |||||||
Men: NA | Indians: 12.6/1000 | |||||||
Whites: 23.1/1000 | ||||||||
Dotchin [13], 2008 | Tanzania | Community | Cross-sectional | 161,071 inhabitants | UKPDS Brain Bank criteria | Overall: 40/100,000 | N: 32; PD:100% | Prevalence is adjusted to UK population. Mean duration 5.1 y |
Men: 64/100,000 | ||||||||
women: 20/100,000 | Age (at onset): 69y (29–90) | |||||||
Men: 72% | ||||||||
Schoenberg [14], 1988 | Nigeria | Community | Cross-sectional | Black population aged 40 + 3412 participants | Clinical | Age adjusted: 67/100,000 | N: 2; PD:100% |  |
Age: NA | ||||||||
Men: NA | ||||||||
USA | Community | Cross-sectional | Black population aged 40 + 3521 black participants and 5404 white participants. | Clinical | Age adjusted: | N: 12; PD: 100% |  | |
Age: NA | ||||||||
Blacks: 341/100,000 | Men: NA | |||||||
Whites: 352/100,000 | ||||||||
Winkler [15], 2010 | Tanzania | Hospital | Cross-sectional | n = 8676 patients admitted (740 with neurological diseases) | UKPDS Brain Bank criteria | 1/1,000 (all patients) | N: 8; PD:37% |  |
2003 | 11/1,000 (Patients with neurological diseases | |||||||
Age: ≥32 y | ||||||||
Men: 100% | ||||||||
Community | Cross-sectional | 1569 people, age 50–110 years | UKPDS Brain Bank criteria | 235/100,000 | N: 0 | None of the 18 screened-positive was confirmed as having PD. Poisson distribution used to estimate the prevalence. | ||
2003-2005 | ||||||||
Kengne [16], 2006 | Cameroon | Hospital | Cross-sectional | 4041 patients in a neurology clinic145 (3.9%) had neurodegenerative diseases | Not provided | 488/1,000 of all neurodegenerative diseases; 10.1/1,000 of all neurologic consultation | N: 41; PD 100% | 4 selected neurodegenerative brain disorders: dementia, PD, ALS, chorea |
1993-2001 | Age: 15-84 y | |||||||
Men: 73.2% | ||||||||
Lombard [17],1978 | Zimbabwe | Hospital | Cross-sectional | Total patients admitted: 83,453 blacks, 34,952 whites | Not provided | Blacks: 0.21/1,000 | N: 50 (17 blacks) | Retrospective review of medical files |
Whites: 2.83/1,000 | Age/men: NA | |||||||
Osuntokun [18], 1979 | Nigeria | Hospital | Cross-sectional | 217 patients with parkinsonism | Not provided | NA | N: 217; PD 38% | All patients evaluated by the authors |
1966-1976 | Age: median 51-70 y, | |||||||
Men:75% | ||||||||
Osuntokun [19], 1987 | Nigeria | Community | Cross-sectional | Total participants surveyed: 18,954 | Not provided | 10/100,000 | N. 2; PD 100% | Screening Questionnaire developed by author |
1985 | Age/men: NA | |||||||
Haylett [20], 2012 | South Africa | Hospital | Cross-sectional | 229 patients with PD including 163 whites (71%), 45 mixed ancestry (20%), 17 blacks (7%) and 4 Indians (2%) | UKPDS Brain Bank criteria | NA | N: 229; PD 100% | Mutation in the Parkin gene |
Age (at onset): 54 y (17–80) | Homozygous or compound heterozygous mutations: 7 patients | |||||||
Heterozygous variant: 7 | ||||||||
Men: % NA | ||||||||
Ekenze [21], 2010 | Nigeria | Hospital | Cross-sectional | 8440 admission in the medical ward; 1249 had neurological diseases (men 640) | Not specified | 21.9/1000 of al neurological admissions | N: 14 | Â |
2003-2007 | Age ≥ 70 y (71%) | |||||||
Men: 28.6% | ||||||||
Owolabi [22], 2010 | Nigeria | Hospital | Cross-sectional | 6282 admission in the medical ward; 980 had neurological diseases (men 586) | Clinical: any 3 out of tremor, rigidity, Akinesia/bradikinesia/postural and instability | 4.1/1,000 of all neurological admissions | N: 4 | Â |
2005-2007 | Age: (50–68) | |||||||
Men; 100% | ||||||||
Okubadejo [23], 2004 | Nigeria | Hospital | Case–control | 33 participants (men 25, mean age 60 y) with PD and 33 match controls | Any 3 out of tremor, rigidity, Akinesia/bradikinesia/postural and instability | NA | N: 33 | Case fatality rate was higher in PD (25% vs. 7.1%), Factors associated with increased mortality: advanced age and disease severity |
Age (at onset): 36-80y | ||||||||
Men: 75% | ||||||||
Okubadejo [24], 2005 | Nigeria | Hospital | Case–control | 28 participants (men 21, mean age 63 y) with PD and 28 match controls | Any 2 out of tremor, rigidity, Akinesia/bradikinesia/postural and instability, exclusion of other causes of parkinsonism | NA | N: 28; PD 100% | Autonomic dysfunction rate was higher in PD (61% vs. 6%), |
Age (at onset): 37-76 y | ||||||||
Men: 76% | ||||||||
Okubadejo [25], 2010 | Nigeria | Hospital | Cross-sectional | 124 participants with Parkinsonism in a neurology clinic | Any 3 of the following: tremors, rigidity, bradykinesia, and postural or gait abnormality | 15/1,000 of all neurological consultations | N: 98; PD 79% | Other causes of parkinsonism n(%): Vascular/drug induced/MSA/LBD: 9(35)/5(19)/4(15)/3(11) |
1996-2006 | ||||||||
Age (at onset): 61y Men: 76.5% | ||||||||
Keyser [26], 2010 | South Africa | Hospital | Cross-sectional | 154 patients with PD including 51 whites (35%), 45 Afrikaners (31%), 29 mixed ancestry (20%), 17 blacks (12%) and 3 Indians (2%). | UK Parkinson’s Disease UKPDS Brain Bank criteria | NA | N: 154; PD 100% | 16 sequence variants of the PINK1gene identified: 1 homozygous mutation (Y258X), 2 heterozygous missense variants (P305A and E476K), and 13 polymorphisms |
Age (at onset): 52 y | ||||||||
Men: 62% | ||||||||
Van Der Merwe [27], 2012 | South Africa | Hospital | Cross-sectional | 111 patients with early onset PD (men 71) and 286 with late onset PD (men 62%) from a movement disorder clinic | UKPDS Brain Bank criteria | NA | N: 397; PD 100% | A positive family history was associated with a younger age at onset. |
2007-2011 | Age (at onset): 57 y Men: 248 | |||||||
Femi [28], 2012 | Nigeria | Hospital | Cross-sectional | 1153 participants in 2 Neurologic clinics; 96 (men: 74) had parkinsonism | presence of at least three of the four cardinal features of tremors, rigidity, bradykinesia, and postural or gait abnormality | 69.4/1,000 of all neurological consultations | N: 96; PD (83.3%) | Â |
2007-2011 | ||||||||
Age: 58 y | ||||||||
Men: 63.5% | ||||||||
Cilia [29], 2012 | Ghana | Hospital | Case–control | 54 participants with PD and 46 healthy participants | UKPDS Brain Bank criteria | NA | N: 54; PD 100% | Leucine-rich repeat kinase 2 (LRRK2) gene found in no participants |
Age (at onset): 59 y (30–83) | ||||||||
 |  |  |  |  |  |  | Men: 61% |  |