Low serum vitamin B12 is common in coeliac disease and is not due to autoimmune gastritis

被引:51
作者
Dickey, W [1 ]
机构
[1] Altnagelvin Hosp, Dept Gastroenterol, Londonderry BT47 6SB, North Ireland
关键词
coeliac disease; gastric atrophy; villous atrophy; vitamin B12;
D O I
10.1097/00042737-200204000-00016
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Objective Although coeliac disease is a disorder of the proximal small bowel, associated vitamin B12 deficiency has been reported. This study aimed to assess the prevalence of 1312 deficiency in a large series of coeliac patients, and to exclude the possibility that it is due to associated autoimmune gastritis. Design Prospective routine measurement of serum 13112 in coeliac patients, with investigations for pernicious anaemia/autoimmune gastritis in 1311 2-deficient patients. Setting Gastroenterology department of a large district general hospital. Interventions If they were not taking vitamin B12 supplements already, patients had serum B12 measured before starting dietary gluten exclusion. Those with low levels also had gastric biopsies taken and plasma gastrin and serum gastric parietal cell and intrinsic factor antibodies measured. Main outcome measures Prevalence of low serum B12, and presence or absence of indicators of pernicious anaemia/autoimmune gastritis in patients with low serum B12. Results Of 159 patients, 13 had low serum B12 at diagnosis. A further six had been receiving B12 replacement therapy for 3-37 years before diagnosis, giving an overall prevalence of 12% (19 patients). Only 2/19 patients had gastric corpus atrophy, one with intrinsic factor antibodies and the other with hypergastrinaemia. There was no relationship between low 1312 and clinical characteristics. Conclusions Low 1312 is common in coeliac disease without concurrent pernicious anaemia, and may be a presenting manifestation. B12 status should be known before folic acid replacement is started. (C) 2002 Lippincott Williams Wilkins.
引用
收藏
页码:425 / 427
页数:3
相关论文
共 17 条
[1]  
ALLEN RH, 1978, J CLIN INVEST, V61, P1728
[2]   Symptoms and haematologic features in consecutive adult coeliac patients [J].
Bode, S ;
GudmandHoyer, E .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 1996, 31 (01) :54-60
[3]  
CARMEL R, 1992, CLIN EXP IMMUNOL, V89, P74
[4]  
Catassi C, 2001, EUR J GASTROEN HEPAT, V13, P1123
[5]   GENDER AND CLINICAL PRESENTATION IN ADULT CELIAC-DISEASE [J].
CIACCI, C ;
CIRILLO, M ;
SOLLAZZO, R ;
SAVINO, G ;
SABBATINI, F ;
MAZZACCA, G .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 1995, 30 (11) :1077-1081
[6]   CELIAC-DISEASE - ASSOCIATED DISORDERS AND SURVIVAL [J].
COLLIN, P ;
REUNALA, T ;
PUKKALA, E ;
LAIPPALA, P ;
KEYRILAINEN, O ;
PASTERNACK, A .
GUT, 1994, 35 (09) :1215-1218
[7]  
Collins B J, 1986, Pancreas, V1, P143, DOI 10.1097/00006676-198603000-00006
[8]  
Dahele A, 2001, AM J GASTROENTEROL, V96, P745, DOI 10.1111/j.1572-0241.2001.03616.x
[9]   LONGITUDINAL-STUDY OF CIRCULATING GASTRIC ANTIBODIES IN PERNICIOUS-ANEMIA [J].
DAVIDSON, RJL ;
ATRAH, HI ;
SEWELL, HF .
JOURNAL OF CLINICAL PATHOLOGY, 1989, 42 (10) :1092-1095
[10]   Celiac disease and autoimmune endocrinologic disorders [J].
Kaukinen, K ;
Collin, P ;
Mykkänen, AH ;
Partanen, J ;
Mäki, M ;
Salmi, J .
DIGESTIVE DISEASES AND SCIENCES, 1999, 44 (07) :1428-1433