Key result
ACE I/I genotype linked to ~131% greater polydipsia risk in schizophrenia versus D allele.
Why the study?
Previous studies revealed changes in central ACE levels in schizophrenic patients possibly related to polydipsia, and the ACE I/D polymorphism is associated with ACE levels, motivating investigation of its association with schizophrenia and polydipsia.
Is the ACE I/D polymorphism associated with schizophrenia or polydipsia in schizophrenic patients?
Case-Control (n=241)
Is the ACE I/D polymorphism associated with schizophrenia or polydipsia in schizophrenic patients?
Odds Ratio: 2.31 (95% CI 0.95–5.65)
The ACE I/D polymorphism showed no association with schizophrenia but a modest association with polydipsia in schizophrenic patients, requiring further replication.
ACE I/D polymorphism in schizophrenia remains hypothesis-generating; leaves open any link to polydipsia or clinical relevance.
Angiotensin-converting enzyme (ACE) is a key enzyme in the renin-angiotensin system and can modulate dopamine turnover in the midbrain. Previous studies have revealed changes in the central ACE levels for schizophrenic patients, possibly related to the polydipsia commonly demonstrated for chronic schizophrenia. An insertion (I)/deletion (D) polymorphism of the ACE gene has been associated with ACE levels. Therefore, we elected to investigate the ACE I/D polymorphism for 124 schizophrenic patients and 117 control subjects. No significant differences for the genotype distribution or the allele frequency were revealed comparing controls and schizophrenic patients. The ACE genotypes were not associated with onset age or psychiatric symptoms for the schizophrenic cases. A modest association was revealed for this ACE polymorphism and polydipsia diagnosis for these patients. Using bearers of the D allele as baseline, the ratio for I/I homozygote was 2.31 (95% CI 0.95-5.65). This association needs further replication as it may have implications for the pathogenesis and the treatment of polydipsia for schizophrenic patients.
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Ouyang et al. (2001) conducted a case-control in Schizophrenia and Polydipsia (n=241). ACE I/D polymorphism (I/I homozygote) vs. D allele bearers and healthy controls was evaluated on Polydipsia diagnosis in schizophrenic patients (OR 2.31, 95% CI 0.95-5.65). The ACE I/I homozygous genotype was modestly associated with polydipsia in schizophrenic patients compared to D allele bearers (OR 2.31; 95% CI 0.95-5.65).
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