Epidemiology of familial adenomatous polyposis in Sweden:: Changes over time and differences in phenotype between males and females

被引:54
作者
Björk, J [1 ]
Åkerbrant, H
Iselius, L
Alm, T
Hultcrantz, R
机构
[1] Swedish Polyposis Registry, Dept Gastroenterol & Hepatol, Stockholm, Sweden
[2] Karolinska Inst, Karolinska Hosp, Dept Surg, S-10401 Stockholm, Sweden
关键词
colorectal cancer; epidemiology; familial adenomatous polyposis; sex;
D O I
10.1080/003655299750024751
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: The: Swedish Polyposis Registry was set up in Sweden in the late 1950s to promote screening of familial adenomatous polyposis (FAP). The aim of this study was to examine the epidemiology of FAP in Sweden, including the influence of screening on morbidity and mortality in colorectal cancer (CRC). Methods: Four hundred and thirty-one patients (213 males and 218 females) with FAP from 145 families recorded by the Swedish Polyposis Registry were investigated. The effect of screening on morbidity and mortality in CRC was evaluated by comparing the 216 probands with the 215 call-up patients. Three different periods were studied: the pre-screening period (1912-1956), the first screening period (1957-1976), and the second screening period (1977-1996). Results: The mean annual incidence rates during the three periods were 0.2, 1.38, and 0.86 per million, respectively. The birth frequency was calculated to be I in 18,000 between 1947 and 1966, and the prevalence was 32 per million at the end of 1996. The proportion of new mutants among the FAP patients born between 1927 and 1966 was estimated to be 11%. The median age at diagnosis of probands was 39 (range, 11-71) years and did not change over time, although an increase was seen in the subgroup with CRC at diagnosis (P = 0.02). In the call-up group the median age at diagnosis was 22 (range, 3-65) years. Sixty-seven per cent of the probands and 3.3% of the call-up patients had CRC at diagnosis, and the corresponding mortality figures were 44% and 1.9%. The risk among probands of having CRC at diagnosis decreased from 81% to 49% (P = 0.0006). Female probands were diagnosed with symptoms (P = 0.03) and CRC (P = 0.04) earlier than male probands. Conclusions: A nationwide screening program facilitates detection and early diagnosis of FAP. A decrease in CRC morbidity among probands contributed to the improved prognosis. An earlier onset of symptoms and CRC in females indicate that the course of FAP is influenced by sex.
引用
收藏
页码:1230 / 1235
页数:6
相关论文
共 16 条
[1]  
ALM T, 1973, CLIN GASTROENTEROL, V2, P577
[2]  
BERK T, 1981, CAN MED ASSOC J, V124, P1427
[3]   FAMILIAL ADENOMATOUS POLYPOSIS (FAP) - FREQUENCY, PENETRANCE, AND MUTATION-RATE [J].
BISGAARD, ML ;
FENGER, K ;
BULOW, S ;
NIEBUHR, E ;
MOHR, J .
HUMAN MUTATION, 1994, 3 (02) :121-125
[4]   LOCALIZATION OF THE GENE FOR FAMILIAL ADENOMATOUS POLYPOSIS ON CHROMOSOME-5 [J].
BODMER, WF ;
BAILEY, CJ ;
BODMER, J ;
BUSSEY, HJR ;
ELLIS, A ;
GORMAN, P ;
LUCIBELLO, FC ;
MURDAY, VA ;
RIDER, SH ;
SCAMBLER, P ;
SHEER, D ;
SOLOMON, E ;
SPURR, NK .
NATURE, 1987, 328 (6131) :614-616
[5]   The incidence rate of familial adenomatous polyposis - Results from the Danish polyposis register [J].
Bulow, S ;
Nielsen, TF ;
Bulow, C ;
Bisgaard, ML ;
Karlsen, L ;
Moesgaard, F .
INTERNATIONAL JOURNAL OF COLORECTAL DISEASE, 1996, 11 (02) :88-91
[6]  
BULOW S, 1987, DAN MED BULL, V34, P1
[7]   CENTRALIZED REGISTRATION, PROPHYLACTIC EXAMINATION, AND TREATMENT RESULTS IN IMPROVED PROGNOSIS IN FAMILIAL ADENOMATOUS POLYPOSIS - RESULTS FROM THE DANISH POLYPOSIS REGISTER [J].
BULOW, S ;
BULOW, C ;
NIELSEN, TF ;
KARLSEN, L ;
MOESGAARD, F .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 1995, 30 (10) :989-993
[8]  
GEDDEDAHL T, 1988, TIDSSKR NOR LAEGEFOR, V109, P2465
[9]  
GOLDBERG PA, 1995, S AFR MED J, V85, P272
[10]   IDENTIFICATION AND CHARACTERIZATION OF THE FAMILIAL ADENOMATOUS POLYPOSIS-COLI GENE [J].
GRODEN, J ;
THLIVERIS, A ;
SAMOWITZ, W ;
CARLSON, M ;
GELBERT, L ;
ALBERTSEN, H ;
JOSLYN, G ;
STEVENS, J ;
SPIRIO, L ;
ROBERTSON, M ;
SARGEANT, L ;
KRAPCHO, K ;
WOLFF, E ;
BURT, R ;
HUGHES, JP ;
WARRINGTON, J ;
MCPHERSON, J ;
WASMUTH, J ;
LEPASLIER, D ;
ABDERRAHIM, H ;
COHEN, D ;
LEPPERT, M ;
WHITE, R .
CELL, 1991, 66 (03) :589-600