Key result
Anti-gliadin antibodies were significantly more prevalent in Japanese patients with idiopathic cerebellar ataxia (36%) compared to normal controls (2%) (OR 25.6) and disease controls (4%).
Why the study?
Is gluten sensitivity (measured by anti-gliadin antibodies) more prevalent in Japanese patients with idiopathic cerebellar ataxia compared to disease and normal controls?
Case-Control (n=88)
Is gluten sensitivity (measured by anti-gliadin antibodies) more prevalent in Japanese patients with idiopathic cerebellar ataxia compared to disease and normal controls?
Odds Ratio: 25.6 (95% CI 2.66–246)
Absolute Event Rate: 36% vs 2%
p-value: p=<0.001
Gluten sensitivity is significantly more prevalent in Japanese patients with adult-onset sporadic cerebellar ataxia compared to controls, suggesting a potential role for gluten-free diets in a subset of these patients.
Supports association of gluten sensitivity with idiopathic cerebellar ataxia; hypothesis-generating and should not yet change practice.
OBJECTIVE: Gluten sensitivity is associated with multiple neurological abnormalities including gluten ataxia, motor neuron disease-like neuropathy, small fiber type neuropathy, cognitive impairment, and even parkinsonism. We investigated whether or not gluten sensitivity is involved in Japanese patients with idiopathic cerebellar ataxia with extracerebellar presentation. PATIENTS OR MATERIALS: Fourteen patients with idiopathic cerebellar ataxia with extracerebellar presentation (autonomic instability, parkinsonism, or pyramidal dysfunction in varying combinations) were screened for anti-gliadin antibodies (AGA) to analyze for the presence or absence of gluten sensitivity. Patients with typical MR findings of multiple system atrophy of the cerebellar type were excluded. As disease controls without cerebellar ataxia, 9 patients with Parkinson's disease and 18 patients with amyotrophic lateral sclerosis were screened for AGA. Forty-seven normal controls were also screened for AGA. RESULTS: We found a high prevalence of AGA in 5 (36%) of 14 cerebellar ataxia patients, but in only 1 (4%) of 27 disease controls without cerebellar ataxia (odds ratio, 14.4; 95% CI, 1.41147; p<0.05) and in only 1 (2%) of 47 normal controls (odds ratio, 25.6; 95% CI, 2.66246; p<0.001). Among the cerebellar ataxia patients, atypical features such as sensorimotor neuropathy and/or mild cognitive impairment were more prevalent in the AGA-positive group (60%) than in the AGA-negative group (0%). In one of the ataxic patients with AGA, a gluten-free diet had positive effects on neurological symptoms and nutritional status. CONCLUSION: Gluten sensitivity is involved in at least some of the unexplained neurological symptoms of Japanese patients with adult-onset, sporadic cerebellar ataxia.
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Ihara et al. (2006) conducted a case-control in Idiopathic cerebellar ataxia with extracerebellar presentation (n=88). Anti-gliadin antibodies (AGA) vs. Normal controls and disease controls without cerebellar ataxia was evaluated on Prevalence of anti-gliadin antibodies (AGA) (OR 25.6, 95% CI 2.66-246, p=<0.001). Anti-gliadin antibodies were significantly more prevalent in Japanese patients with idiopathic cerebellar ataxia (36%) compared to normal controls (2%) (OR 25.6) and disease controls (4%).
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