Table 1.
Results of studies of the epidemiology of olfactory disorders
Population | n | Age (range) | Gender (% Female) | Smell Test | Major findings | Strengths | Weaknesses | Reference |
---|---|---|---|---|---|---|---|---|
Skövde Sweden | 1387 | 20–80 + | 51.77 % | self-report, SOIT | -poorer-than normal odor detection sensitivity was 15.3% (self-report) -the prevalence of olfactory dysfunction was 19.1%; 13.3% had hyposmia and 5.8% suffered from anosmia |
population-based data across all ages; representative of the general adult Swedish population | self-report | 26; 27 |
Skövde Sweden | 1713 | 13–80 + | 52.13 % | self-report | =3.9% of the general population aged 13 years and older report having had parosmia (4.0% of the adults and 3.4% of the teenagers). | added a teenage population; assessed qualitative disorders | teenage data may be less reliable? | 28 |
The Beaver Dam Study WI, USA | 2491 | 53–97 | 58% | SDOIT | -prevalence of impaired olfaction was 24.5% | extensive information available on potential risk factors | limited generalizability to minority groups? | 13 |
The Beaver Dam Offspring Study WI, USA | 1993 | 21–84 | 54.4% | SDOIT | -prevalence of olfactory impairment was low at 3.8% in this primarily middle-aged cohort -this increased with age (from 0.6% in those <35 years to 13.9% among those ≥65 years) |
one of the few longitudinal studies extensive information available on potential risk factors | may not be representative? | 29 |
National Health Interview Survey (NHIS) USA | 80,000 | ≥18 | * | home interview | -1.4% of US adults complained of an olfactory problem -almost 40% of those who reported a chemosensory problem were ≥65 years |
large sample | likely underestimates actual prevalence due to self-report? | 30 |
KNHANES South Korea (2009) | 7306 | 20–95 | 56.7% | questionnaire | -prevalence of subjective olfactory disorders was 4.5% | large sample provided a clinical association between olfactory dysfunction and mental health | self-report, not strictly controlled | 31 |
KNHANES South Korea (2010–201 1) | 11972 | ≥19 | 50.74 % | questionnaire | -prevalence of olfactory dysfunction was 5.0% | large sample provided a clinical association between olfactory dysfunction and mental health | unable to distinguish degrees of smell disturbance; cross-sectional | 32 |
NSHAP, USA | 3005 | 57–85 | 56.7% | Odor ID test | -prevalence of severe olfactory dysfunction was 2.7% | nationally representative sample | only a small percentage of the variance is explained | 33 |
NSHAP, USA | 1436 | 57–85 | 51.7% | Odor ID test | -odor identification is one of the strongest predictors of 5-year mortality | well controlled | no cause of death, no information on younger ages, acquired causes | 1 |
OLFACAT Catalonia, Spain | 9348 | 5–91 | 65.7% | Odor ID test | -prevalence of dysfunction was 19.4% - a significant age-related decline in odor detection |
large sample | potential bias in this non-random sample; lack of ethnic diversity, socio-cultural class | 36 |
Memory and Aging Project (MAP) IL, USA | 481 | mean age 80.6 ± 7.0 | 72.6% | CC-SIT | -prevalence of olfactory impairment was 55.3% -impaired odor identification in old age is associated with impaired global cognition |
high rate of participation in follow-up outstanding cognitive assessment | select cohort of convenience; fewer women included | 42 |
Memory and Aging Project (MAP) IL, USA | 1162 | mean age 79.7 ± 7.7 | 74.5% | CC-SIT | -difficulty identifying familiar odors in old age is associated with increased risk of death | well characterized cohort | select cohort; fewer women included | 45 |
Blue Mountains Eye Study Australia | 1636 | ≥60 | 58.1% | SDOIT | -prevalence of olfactory impairment was 27.0%. | high participation rate high follow-up rate | cross-sectional, potential bias? | 46 |
Bet.ula Sweden | 1906 | 45–90 | 54.46 % | SOIT | -a gradual/linear deterioration in cued odor identification across the adult life span | good demographic and cognitive variables, sample size | cross-sectional | 48 |
Honolulu-Asia Aging Study (HAAS) HI, USA | 2267 | 71–95 | 0% | CCSIT | -olfactory deficits associated with the presence of incidental Lewybodies and PD | longitudinal design, large sample size with excellent follow-up, well-validated test instruments | men only; older age focused | 39 |
not provided