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Hi ;

I think it was 1989-1990:

_________________________

Z Gastroenterol Verh. 1989 Jul;24:136.

Treatment of primary sclerosing cholangitis with ursodeoxycholic acid

Stiehl A, Raedsch R

PMID: 2474928

_________________________

Dig Dis Sci. 1989 Dec;34(12 Suppl):59S-65S.

Effect of different doses of ursodeoxycholic acid in chronic liver

disease.

Podda M, Ghezzi C, Battezzati PM, Bertolini E, Crosignani A, Petroni

ML, Zuin M

Istituto di Medicina Interna, University of Milan, Italy.

Recent clinical studies have indicated that ursodeoxycholic acid

(ursodiol), administered at dosages ranging between 10 and 15

mg/kg/day, improves liver function indices in both cholestatic and

inflammatory chronic liver diseases. These dosages would be

considered high for the use of ursodiol in gallstone dissolution

therapy. To investigate the dose-response relationship to ursodiol

administration, we planned a few studies in patients with primary

biliary cirrhosis (PBC), primary sclerosing cholangitis (PSC), and

chronic hepatitis (CH). Patients with PBC were subdivided into two

groups on the basis of their serum bilirubin values, with 2 mg/dl as

the dividing line. Ursodiol was given at dosages of 250, 500, and 750

mg/day for consecutive periods of two months, the order of treatment

being randomly assigned to each patient. The enrichment with ursodiol

of biliary bile acids was similar in both PBC and CH and, within the

PBC group, in both anicteric and icteric patients. Highly significant

decreases in serum enzyme levels were observed in all groups with the

250 mg/day dose, corresponding to about 4-5 mg/kg/day. The two higher

doses induced further improvements in serum enzyme levels, especially

in patients with PBC, but no significant differences were found

between the 500 and the 750 mg/day doses. The improvements were

roughly proportional to the enrichment of conjugated biliary bile

acids with ursodiol. Serum bilirubin levels, an important prognostic

factor in PBC, were also significantly reduced by ursodiol

administration in patients with initial serum levels higher than 2

mg/dl. The present study indicated that ursodiol is a potentially

useful drug for chronic liver disease.(ABSTRACT TRUNCATED AT 250

WORDS) PMID: 2598769.

_______________________________

J Hepatol. 1990 Jul;11(1):120-3.

Ursodeoxycholic acid for primary sclerosing cholangitis.

Chazouillères O, Poupon R, Capron JP, Metman EH, Dhumeaux D,

Amouretti M, Couzigou P, Labayle D, Trinchet JC

Hôpital Saint-Antoine, Paris, France.

The effects of ursodeoxycholic acid (UDCA, 750-1250 mg/day) were

evaluated prospectively in 15 patients with primary sclerosing

cholangitis (PSC). Five patients had associated inflammatory bowel

disease. After 6 months of treatment, the proportion of patients

suffering from fatigue or pruritus decreased from 60% to 20% and from

33% to 20%, respectively. No exacerbation of associated disorders was

observed. Serum alkaline phosphatase levels (normal less than 100

IU/l) decreased from 401 +/- 53 to 222 +/- 42 (mean +/- S.E.; p less

than 0.001), those of gamma-glutamyl transpeptidase, (normal less

than 40 IU/l) from 520 +/- 89 to 185 +/- 32 (p less than 0.001) and

those of alanine aminotransferases, (normal less than 30 IU/l) from

79 +/- 12 to 42 +/- 6 (p less than 0.02). In three patients, the

discontinuation of UDCA was associated with an aggravation of the

liver test results. In conclusion, this study shows that 6 months of

treatment with UDCA leads to clinical and biochemical improvements in

patients with PSC. These results suggest that UDCA could be an

effective treatment for PSC, and may justify a controlled therapeutic

trial. PMID: 1975818.

_______________________

Gastroenterology. 1990 Aug;99(2):533-5.

Asymptomatic primary sclerosing cholangitis treated with

ursodeoxycholic acid.

Hayashi H, Higuchi T, Ichimiya H, Hishida N, Sakamoto N

Third Department of Medicine, Nagoya University School of Medicine,

Japan.

Ursodeoxycholic acid treatment (600 mg/day) was evaluated in a

patient with asymptomatic primary sclerosing cholangitis. Serum

levels of biliary enzymes decreased to normal ranges within 1 month's

treatment and remained normal for 26 months. Serum chenodeoxycholic

acid had been replaced by ursodeoxycholic acid, and hepatic copper

metabolism, assessed by x-ray probe analysis, improved during the

treatment. However, neither biliary tract sclerosis nor portal tract

pathology changed with the treatment. These observations suggest that

ursodeoxycholic acid protects the liver in primary sclerosing

cholangitis by improving the metabolism of bile acid and copper.

PMID: 2365199

_______________________________

Dave

(father of (23); PSC 07/03; UC 08/03)

>

> Does anyone know when Urso was first used for PSC (not PBC)? Just

> curious.

>

> Cheers,

>

>

>

Link to comment
Share on other sites

Hi ;

I think it was 1989-1990:

_________________________

Z Gastroenterol Verh. 1989 Jul;24:136.

Treatment of primary sclerosing cholangitis with ursodeoxycholic acid

Stiehl A, Raedsch R

PMID: 2474928

_________________________

Dig Dis Sci. 1989 Dec;34(12 Suppl):59S-65S.

Effect of different doses of ursodeoxycholic acid in chronic liver

disease.

Podda M, Ghezzi C, Battezzati PM, Bertolini E, Crosignani A, Petroni

ML, Zuin M

Istituto di Medicina Interna, University of Milan, Italy.

Recent clinical studies have indicated that ursodeoxycholic acid

(ursodiol), administered at dosages ranging between 10 and 15

mg/kg/day, improves liver function indices in both cholestatic and

inflammatory chronic liver diseases. These dosages would be

considered high for the use of ursodiol in gallstone dissolution

therapy. To investigate the dose-response relationship to ursodiol

administration, we planned a few studies in patients with primary

biliary cirrhosis (PBC), primary sclerosing cholangitis (PSC), and

chronic hepatitis (CH). Patients with PBC were subdivided into two

groups on the basis of their serum bilirubin values, with 2 mg/dl as

the dividing line. Ursodiol was given at dosages of 250, 500, and 750

mg/day for consecutive periods of two months, the order of treatment

being randomly assigned to each patient. The enrichment with ursodiol

of biliary bile acids was similar in both PBC and CH and, within the

PBC group, in both anicteric and icteric patients. Highly significant

decreases in serum enzyme levels were observed in all groups with the

250 mg/day dose, corresponding to about 4-5 mg/kg/day. The two higher

doses induced further improvements in serum enzyme levels, especially

in patients with PBC, but no significant differences were found

between the 500 and the 750 mg/day doses. The improvements were

roughly proportional to the enrichment of conjugated biliary bile

acids with ursodiol. Serum bilirubin levels, an important prognostic

factor in PBC, were also significantly reduced by ursodiol

administration in patients with initial serum levels higher than 2

mg/dl. The present study indicated that ursodiol is a potentially

useful drug for chronic liver disease.(ABSTRACT TRUNCATED AT 250

WORDS) PMID: 2598769.

_______________________________

J Hepatol. 1990 Jul;11(1):120-3.

Ursodeoxycholic acid for primary sclerosing cholangitis.

Chazouillères O, Poupon R, Capron JP, Metman EH, Dhumeaux D,

Amouretti M, Couzigou P, Labayle D, Trinchet JC

Hôpital Saint-Antoine, Paris, France.

The effects of ursodeoxycholic acid (UDCA, 750-1250 mg/day) were

evaluated prospectively in 15 patients with primary sclerosing

cholangitis (PSC). Five patients had associated inflammatory bowel

disease. After 6 months of treatment, the proportion of patients

suffering from fatigue or pruritus decreased from 60% to 20% and from

33% to 20%, respectively. No exacerbation of associated disorders was

observed. Serum alkaline phosphatase levels (normal less than 100

IU/l) decreased from 401 +/- 53 to 222 +/- 42 (mean +/- S.E.; p less

than 0.001), those of gamma-glutamyl transpeptidase, (normal less

than 40 IU/l) from 520 +/- 89 to 185 +/- 32 (p less than 0.001) and

those of alanine aminotransferases, (normal less than 30 IU/l) from

79 +/- 12 to 42 +/- 6 (p less than 0.02). In three patients, the

discontinuation of UDCA was associated with an aggravation of the

liver test results. In conclusion, this study shows that 6 months of

treatment with UDCA leads to clinical and biochemical improvements in

patients with PSC. These results suggest that UDCA could be an

effective treatment for PSC, and may justify a controlled therapeutic

trial. PMID: 1975818.

_______________________

Gastroenterology. 1990 Aug;99(2):533-5.

Asymptomatic primary sclerosing cholangitis treated with

ursodeoxycholic acid.

Hayashi H, Higuchi T, Ichimiya H, Hishida N, Sakamoto N

Third Department of Medicine, Nagoya University School of Medicine,

Japan.

Ursodeoxycholic acid treatment (600 mg/day) was evaluated in a

patient with asymptomatic primary sclerosing cholangitis. Serum

levels of biliary enzymes decreased to normal ranges within 1 month's

treatment and remained normal for 26 months. Serum chenodeoxycholic

acid had been replaced by ursodeoxycholic acid, and hepatic copper

metabolism, assessed by x-ray probe analysis, improved during the

treatment. However, neither biliary tract sclerosis nor portal tract

pathology changed with the treatment. These observations suggest that

ursodeoxycholic acid protects the liver in primary sclerosing

cholangitis by improving the metabolism of bile acid and copper.

PMID: 2365199

_______________________________

Dave

(father of (23); PSC 07/03; UC 08/03)

>

> Does anyone know when Urso was first used for PSC (not PBC)? Just

> curious.

>

> Cheers,

>

>

>

Link to comment
Share on other sites

It must be about that long ago (1990) that I started on it. In all that time, I have not had any physical indication that it was doing anything at all.

On another topic, does anyone suffer from psoriasis? Some sources say that cyclosporin helps. I'm not going there. My TX Doc says that if you have one autoimmune disease, you'll get some more. Very comforting.

Don

Please be a blood/organ donor

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Share on other sites

It must be about that long ago (1990) that I started on it. In all that time, I have not had any physical indication that it was doing anything at all.

On another topic, does anyone suffer from psoriasis? Some sources say that cyclosporin helps. I'm not going there. My TX Doc says that if you have one autoimmune disease, you'll get some more. Very comforting.

Don

Please be a blood/organ donor

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Share on other sites

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