Mitochondrial diabetes, DIDMOAD and other inherited diabetes syndromes

被引:20
作者
Barrett, TG [1 ]
机构
[1] Univ Birmingham, Birmingham B15 2TT, W Midlands, England
[2] Birmingham Childrens Hosp, Dept Endocrinol, Birmingham B4 6NH, W Midlands, England
关键词
mitochondria; Wolfram syndrome; DIDMOAD; Alstrom syndrome; Wolcott-Rallison syndrome; leprechaunism; Bardet-Biedl syndrome; Prader-Willi syndrome;
D O I
10.1053/beem.2001.0149
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Inherited diabetes syndromes are individually rare but collectively make up a significant proportion of patients attending diabetes clinics, some of whom have multiple handicaps. This chapter focuses on syndromes in which major advances have been made in our understanding of the underlying molecular genetics. These conditions demonstrate novel genetic mechanisms such as maternal inheritance and genetic imprinting. They are also fascinating as they aid our understanding of insulin metabolism, both normal and abnormal. As the causative genes are identified, future issues will be the availability of genetic testing, their contribution to the genetic heterogeneity of the more common types of diabetes, and functional studies of the relevant proteins. It is probable that other subtypes of diabetes will be identified as the relevant metabolic pathways are characterized. This is an exciting time to be a diabetes physician as diabetology returns to being a diagnostic rather than a mainly management-based speciality.
引用
收藏
页码:325 / 343
页数:19
相关论文
共 101 条
[1]   DIABETES-MELLITUS, THIAMINE-DEPENDENT MEGALOBLASTIC-ANEMIA, AND SENSORINEURAL DEAFNESS ASSOCIATED WITH DEFICIENT ALPHA-KETOGLUTARATE DEHYDROGENASE-ACTIVITY [J].
ABBOUD, MR ;
ALEXANDER, D ;
NAJJAR, SS .
JOURNAL OF PEDIATRICS, 1985, 107 (04) :537-541
[2]  
Alstrom C.H., 1959, ACTA PSYCH NEUROL SC, V129, P1
[3]   Missense variations of the gene responsible for Wolfram syndrome (WFS1/wolframin) in Japanese:: Possible contribution of the Arg456His mutation to type 1 diabetes as a nonautoimmune genetic basis [J].
Awata, T ;
Inoue, K ;
Kurihara, S ;
Ohkubo, T ;
Inoue, I ;
Abe, T ;
Takino, H ;
Kanazawa, Y ;
Katayama, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 268 (02) :612-616
[4]   MATERNALLY TRANSMITTED DIABETES AND DEAFNESS ASSOCIATED WITH A 10.4 KB MITOCHONDRIAL-DNA DELETION [J].
BALLINGER, SW ;
SHOFFNER, JM ;
HEDAYA, EV ;
TROUNCE, I ;
POLAK, MA ;
KOONTZ, DA ;
WALLACE, DC .
NATURE GENETICS, 1992, 1 (01) :11-15
[5]  
BARDET G, 1920, THESIS PARIS
[6]   The mitochondrial genome in Wolfram syndrome [J].
Barrett, TG ;
Scott-Brown, M ;
Seller, A ;
Bednarz, A ;
Poulton, K ;
Poulton, J .
JOURNAL OF MEDICAL GENETICS, 2000, 37 (06) :463-466
[7]   Muscle biochemistry in thiamin-responsive anaemia [J].
Barrett, TG ;
Poulton, K ;
Baines, M ;
McCowen, C .
JOURNAL OF INHERITED METABOLIC DISEASE, 1997, 20 (03) :404-406
[8]   NEURODEGENERATION AND DIABETES - UK NATIONWIDE STUDY OF WOLFRAM (DIDMOAD) SYNDROME [J].
BARRETT, TG ;
BUNDEY, SE ;
MACLEOD, AF .
LANCET, 1995, 346 (8988) :1458-1463
[9]   Optic atrophy in Wolfram (DIDMOAD) syndrome [J].
Barrett, TG ;
Bundey, SE ;
Fielder, AR ;
Good, PA .
EYE, 1997, 11 (6) :882-888
[10]  
Barrientos A, 1996, AM J HUM GENET, V58, P963