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Multivariate analysis showed that the risk ratio for the development of response in patients with serum HBV-DNA level of less than 200 Meq/ml was 3.60 compared with patients with that of 200 Meq/ml or more than 200 Meq/ml (95% CI, 1.012 12.81).
As it was a retrospective study, due to unavailability of all records, there was an inability to analyze electrolytes and there relation with the BUN/Creatinine ratio for the development of pre renal failure.
The likelihood ratio for the development of carcinomatous meningitis again significantly correlated with breast cancer subtype.
We did not find a significant odds ratio for the development of fHCM for cats heterozygous for the mutation.
The Cox proportional hazards model was used to estimate the hazard ratio for the development of diabetes between the groups.
The hazard ratio for the development of dementia was 1.16 for patients who had POCD at 1 week, and 1.50 for patients with POCD at 3 weeks.
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The adjusted odds ratios for the development of three-vessel disease were 2.80 (95% confidence interval 1.06 7.37; P=.038) for PON1 codon 192 Arg/Arg and 3.68 (95% confidence interval 1.26 10.68; P=.017) for PON2 codon 311 Cys/Cys.
The odds ratios for the development of ROP were greatest in infants weighing less than 1250 grams.
Unadjusted odds ratios for the development of diabetes are shown in Table 1.
Statistical analyses included Cox regression for calculating risk ratios of survival endpoints and logistic regression for determining odds ratios for the development of loco-regional recurrences.
The odds ratios for the development of simvastatin-induced myopathy were 4.5 and 16.9 for heterozygous and homozygous C allele transitions at this single nucleotide polymorphism.
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