• 沒有找到結果。

嚴重病毒性肝硬化病人血清鋅值與白蛋白的關係

N/A
N/A
Protected

Academic year: 2021

Share "嚴重病毒性肝硬化病人血清鋅值與白蛋白的關係"

Copied!
7
0
0

加載中.... (立即查看全文)

全文

(1)

2005 16 11-17

92

1 2 1 2 1 1 1 2 1 1

1

2

2002 2004

20~80

2 mg/dl

31 16 15

59.3 11.7 B C 22 9 Child-Pugh A,B, C

1, 24 6 7.25 0.83 gm/dl 3.24 0.57 gm/dl

2.47 2.1 mg/dl 150.9 93.1 mg/dl 72.2 22.9 mg/dl

662.4 121.5 g/L R = 0.644

P = 0.034

3.5 gm/dl 700 g/L

( Liver cirrhosis ) ( Zinc )

( Albumin )

(2)

1

2

3-4 5

6

7 - 8

9

10

4

11

2 0 0 2

2 0 0 4 B C

20~80 Child-Puph B C

Child-Puph C

B C

Furosemide ( 40 mg ) spironolactone (25 mg )

2 mg/dl

(3)

( simple linear regression ) SPSS

3 1

16 15

59.3 11.7 B

22 C 9 61.3 10.1

157.8 11.1

Child-Pugh ( )

B

6 A 2 3

10.94 1.77 gm/dl 4730 2200/mm3

22.4 14.1%

84.3 43.4K 13.8 1.6 INR 1.3 1.4

7.25 0.83 gm/dl 3.24

0.57 gm/dl ( 19 3.5 gm/dl ) 2.47 2.1 mg/dl

150.9 93.1 mg/dl 72.2 22.9

mg/dl ( ) 662.4 121.5 g/L

790 g/L

R = 0.644, B=136.3, Alpha=220.6, CI= 0.95, P = 0.034 ( )

Child-Pugh

( )

13

16 15

22 9 Child-Pugh

1* 24

6

*

Child-Pugh

(4)

1 9 6 0

12 1974

300

( alkaline phosphatase ) 2 0 0 0

( transcription factors )

13

14-15 16

15mg

1 2 m g 1 5 -

25mg

( malabsorption syndrome )

17

18

(%) 22.4 14.1 20-40 0.959

(x1000/mm3) 84.3 43.4 140-450 0.179

PT ( ) 13.8 1.6 9-13 0.207

INR 1.35 0.29 < 2 0.219

(gm/dl) 106.8 37.8 70-120 0.055

(gm/dl) 7.25 0.83 6-8 0.457

(gm/dl)* 3.24 0.57 3.5-5.0 0.034

(mg/dl) 2.47 2.1 0.2-1.3 0.627

(mg/dl) 0.84 1.30 < 0.4 0.469

(u/l) 115.7 60.1 35-104 0.866

GOT(u/l) 73.7 34.2 5-35 0.526

GPT(u/l) 48.1 21.0 5-30 0.733

(mg/dl) 150.9 93.1 130-230 0.716

(mg/dl) 72.2 22.9 35-165 0.915

(mg/dl) 0.98 0.25 0.5-1.3 0.184

( g/L) 662.4 121.5

* p < 0.05

(5)

19

3.5 gm/dl 7 0 0 g / L 3.5 gm/dl 19

7 0 0 g / L

20

585

21

22

1.

2.

3.5gm/dl 3.

4.

1.Crawford DH, Cuneo RC, Shepherd RW. Pathogenesis and assessment of malnutrition in liver disease. J Gastroenterol Hepatol 1993; 8: 89-94.

2.Poo JL, Rosas-Romero R, Rodriguez F, et al. Serum zinc con- centrations in two cohorts of 153 healthy subjects and 100 cir- rhotic patients from Mexico City. Dig Dis 1995; 13: 136-42.

3.Kojima-Yuasa A, Ohkita T, Yukami K, et al. Involvement of in- tracellular glutathione in zinc deficiency-induced activation of hepatic stellate cells. Chem Biol Interact 2003; 146: 89-99.

4.Yoshida Y, Higashi T, Nouso K, et al. Effects of zinc deficien- cy/zinc supplementation on ammonia metabolism in patients with decompensated liver cirrhosis. Acta Med Okayama 2001;

55: 349-55.

5.Bresci G, Parisi G, Banti S. Management of hepatic en- cephalopathy with oral zinc supplementation: a long-term treat- ment. Eur J Med 1993; 2: 414-6.

6.Ozbal E, Helvaci M, Kasirga E, Akdenizoglu F, Kizilgunesler A. Serum zinc as a factor predicting response to interferon- alpha2b therapy in children with chronic hepatitis B. Biol Trace Elem Res 2002; 90: 31-8.

7.Kugelmas M. Preliminary observation: oral zinc sulfate re- placement is effective in treating muscle cramps in cirrhotic patients. J Am Coll Nutr 2000; 19: 13-5.

8.Baskol M, Ozbakir O, Coskun R, Baskol G, Saraymen R, Yucesoy M. The role of serum zinc and other factors on the prevalence of muscle cramps in non-alcoholic cirrhotic patients.

J Clin Gastroenterol 2004; 38: 524-9.

15

(6)

holic cirrhosis with diet therapy. Trop Gastroenterol 1995; 16:

119-22.

12.Black RE. Zinc deficiency, infectious disease and mortality in the developing world. J Nutr 2003; 133: 1485S-9S.

13.Coleman JE. Zinc proteins: enzymes, storage proteins, tran- scription factors, and replication proteins. Annu Rev Biochem 1992; 61: 897-946.

14.Beck FW, Prasad AS, Kaplan J, Fitzgerald JT, Brewer GJ.

Changes in cytokine production and T cell subpopulations in ex- perimentally induced zinc-deficient humans. Am J Physiol 1997; 272: E1002-7.

15.Diez RA, Gil EB, Gutierrez GF, Munoz RC. Serum im- munoglobulins and T cell subpopulations in alcoholic cirrhosis after oral zinc therapy. Gastroenterol Clin Biol 1988; 12: 584.

with advanced cirrhosis. Hepatology 1996; 23: 1084-92.

20.Bal W, Christodoulou J, Sadler PJ, Tucker A. Multi-metal bind- ing site of serum albumin. J Inorg Biochem 1998; 70: 33-9.

21.Stewart AJ, Blindauer CA, Berezenko S, Sleep D, Sadler PJ.

Interdomain zinc site on human albumin. Proc Natl Acad Sci USA 2003; 100: 3701-6.

22.Hocke M, Winnefeld K, Bosseckert H. Oral zinc therapy in pa- tients with supposed mild zinc deficiency--a critical review. Z Gastroenterol 2001; 39: 83-8.

(7)

17

Correlation Between Serum Zinc and

Albumin Level in Severe Viral Cirrhosis Patients

Tsang-En Wang1, 2, Ming-Jen Chen1, 2, Shou-Chuan Shih1, 2, Chia-Yung Lieu1, Cheng-Hsin Chu1, 2, Horng-Yuan Wang1, and Wen-Hsinug Chang1

Zinc is an important trace element and it participates in metabolism and several processes of diseases. Zinc deficiency is common in patients with liver cirrhosis and might cause relative complications. Early zinc supple- ment may prevent and improve hepatic encephalopathy and other symptoms of cirrhosis. We investigate the cor- relations between serum biochemistry data and serum zinc level and try to seek a land marker for detecting zinc deficiency in general practice. From Sep 2002 to Jun 2004, we collected serum biochemistry profiles and zinc level in patients with stable advanced viral cirrhosis. Thirty-one patients (16 men and 15 women) at the age of 20 to 80 years old who had Child-Pugh grade B and C cirrhosis were enrolled in this study. The excluded crite- ria were alcoholic dependant, recent blood transfusion or systemic infections, abnormal renal function, and large amount diuretic or steroid use. Twenty-two patients had chronic hepatitis B and 9 patients had chronic hepatitis C. The mean serum albumin was 3.24±0.57 gm/dl and mean serum zinc was 662.4±121.5 g/L. The correla- tions were analyzed by linear regression. Serum zinc level is related to albumin level in these cirrhotic patients ( R = 0.644 P = 0.034 ). There is no correlation between zinc and total protein, grade of cirrhosis and other bio- chemistry parameters. We concluded that most of viral cirrhotic patients in Taiwan may not have obvious mal- nutrition. The serum zinc is usually lower and has significant relation to the serum albumin level. Albumin below the lower normal limit 3.5 gm/dl may be a useful clue to detect zinc deficiency that may be induced hepatic en- cephalopathy and general malaise. As we known, not only the improvement of albumin level but also the gene- ral nutrition support is important for increasing serum zinc that might be of benefit for cirrhotic patients. ( J Intern Med Taiwan 2005; 16: 11-17 )

1

Division of Gastroenterology, Department of Internal Medicine, Mackay Memorial Hospital, Taipei, Taiwan

2

Mackay Medicine, Nursing and Management College, Taiwan

參考文獻

相關文件

The clinical and radiological features of 6 cases of NBCCS were characterized into major and minor criteria and compared with features reported in Indian patients and in patients

SUMMARY The purpose of this systematic review was to describe the prevalence of whiplash trauma in patients with temporomandibular disorders (TMDs) and to describe clinical signs

The clinical and radiographic records of 208 patients suffering from neurological symptoms in maxillofacial region. They had referred to neurology department and then

Significantly higher serum follicle-stimulating hormone level and a significantly lower serum estradiol level in the menopausal or post-. menopausal women

patients with stage I/II disease but not in those with stage III disease.43 A high serum level of VEGF is associated with poor survival among patients with small cell lung

As seen in Table 1 every one of them occurred in male patients; with the exception of one case all large sized sialoliths were located in the submandibular duct (94.4%) and only

pylori in pathogenesis of oral mucosal lesions or ulcerations is still unclear, it seems that patients with oral lesions as leukoplakia and oral lichen planus, and concurrent

However, in HIV-positive patients, plasma cell tumors may present at unusual sites and progress rapidly to involve multiple sites, including the soft tissues and viscera [19]..