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Table 2 Clinical use of taurine in different pathophysiological conditions

From: Taurine: the appeal of a safe amino acid for skeletal muscle disorders

References

Patients

Dose (g/day or mg/kg)

Duration

Result

Franconi et al. [130]

IDDM (Diabetes mellitus type 1)

1.5 g

90 days

No effect

Elizarova and Nedosugova [131]

IDDM

1 g

30 days

Glucose metabolism and trygliceride level improved

Chauncey et al. [133]

NIDDM (DM type 2)

3 g

4 months

Plasma taurine level increased

Brøns et al. [134]

Overweight non-diabetic

1.5 g

8 weeks

No effect

Xiao et al. [136]

Overweight non-diabetic

3 g

2 weeks

Insulin sensitivity improved

Nakamura et al. [132]

NIDDM with microalbuminemia

3 g

12 months

No effect

Moloney et al. [135]

IDDM

1.5 g

2 weeks

Endotelium-dependent reaction improved

Gonzales-Contreras et al. [142]

Cholestasis by parenteral nutrition

~25 mg/kg/day

~50 days

Hepatoprotection with reduction of AST, ALT and GGT

Rosa et al. [143]

Obesity

3 g/day

8 weeks

Increase in plasma levels of taurine and adiponectin; reduction of inflammatory markers

Pearl et al. [141]

Succinic semialdehyde dehydrogenase deficiency (efficacy, safety and tolerability)

50–200 mg/kg/d (age range 12 years)

13 months (mean time from 3 to 50)

No significant effects

Tolerability issues at highest doses

Fujita et al. [139]

Hypertension

6 g

7 days

Systolic and diastolic pressure improved

Azuma et al. [138]

Congestive heart failure

6 g

4 weeks

Heart parameters improved

Bergamini et al. [137]

Epilepsy

200 mg–21 g

Various

Seizure frequency reduction

Durelli et al. [36]

Dystrophic myotonia

6–10 g

6 months

Myotonic symptoms improvement

Dunn-Lewis et al. [140]

Elderly

500 mg in multinurtient supplement

4 weeks

Physical function improved