Autoimmune diseases in families of French patients with multiple sclerosis

被引:62
作者
Heinzlef, O
Alamowitch, S
Sazdovitch, V
Chillet, P
Joutel, A
Tournier-Lasserve, E
Roullet, E
机构
[1] Hop Tenon, Serv Neurol, F-75020 Paris, France
[2] INSERM, U25, Dept Neurol, Paris, France
来源
ACTA NEUROLOGICA SCANDINAVICA | 2000年 / 101卷 / 01期
关键词
multiple sclerosis; epidemiology; genetics; autoimmunity;
D O I
10.1034/j.1600-0404.2000.101001036.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Multiple sclerosis (MS) is associated with autoimmune disorders (AIDs) in individual patients, and limited data suggest a possible familial association of MS and AIDs; however, no systematic study has been conducted on the occurrence of AIDs in the families of MS patients. Using a standardized interview focused on AIDs, we obtained the family histories of 357 consecutive patients from our MS clinic. Adequate information was obtained on 1971 first-degree relatives. Fifty-five patients (15.4%) had first-degree relatives with MS (n = 22, 6.2%), another AID (n = 30, 8.4%), or both (n = 3, 0.8%). In 16 families (4.5%), at least 3 first-degree relatives had MS or another BID. MS, Grave's disease, rheumatoid arthritis, vitiligo, type 1 insulin-dependent diabetes mellitus, and uveitis, were the most common AIDs in these families. Such multiplex families (families with MS plus AID) are appropriate for identifying susceptibility genes that may be common to MS and other AIDs.
引用
收藏
页码:36 / 40
页数:5
相关论文
共 24 条
  • [1] Clustering of non-major histocompatibility complex susceptibility candidate loci in human autoimmune diseases
    Becker, KG
    Simon, RM
    Bailey-Wilson, JE
    Freidlin, B
    Biddison, WE
    McFarland, HF
    Trent, JM
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (17) : 9979 - 9984
  • [2] Multiple loci for multiple sclerosis
    Bell, JI
    Lathrop, GM
    [J]. NATURE GENETICS, 1996, 13 (04) : 377 - 378
  • [3] BIAS WB, 1986, AM J HUM GENET, V39, P584
  • [4] Chronic autoimmune thyroiditis
    Dayan, CM
    Daniels, GH
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (02) : 99 - 107
  • [5] DEBAKER HWG, 1972, AUS NZ MED J, V3, P256
  • [6] DEKEYSER J, 1988, NEUROLOGY, V38, P371
  • [7] A full genome search in multiple sclerosis
    Ebers, GC
    Kukay, K
    Bulman, DE
    Sadovnick, AD
    Rice, G
    Anderson, C
    Armstrong, H
    Cousin, K
    Bell, RB
    Hader, W
    Paty, DW
    Hashimoto, S
    Oger, J
    Duquette, P
    Warren, S
    Gray, T
    OConnor, P
    Nath, A
    Auty, A
    Metz, L
    Francis, G
    Paulseth, JE
    Murray, TJ
    PrysePhillips, W
    Nelson, R
    Freedman, M
    Brunet, D
    Bouchard, JP
    Hinds, D
    Risch, N
    [J]. NATURE GENETICS, 1996, 13 (04) : 472 - 476
  • [8] A GENETIC-BASIS FOR FAMILIAL AGGREGATION IN MULTIPLE-SCLEROSIS
    EBERS, GC
    SADOVNICK, AD
    RISCH, NJ
    BULMAN, D
    RICE, GPA
    HASHIMOTO, SA
    PATY, D
    OGER, JJF
    METZ, L
    BELL, R
    WARREN, S
    HADER, W
    AUTY, T
    NATH, A
    GRAY, T
    OCONNOR, P
    NELSON, R
    FREEDMAN, M
    BRUNET, D
    PAULSETH, R
    FRANCIS, G
    DUQUETTE, P
    MURRAY, TJ
    BAHN, V
    PRYSEPHILLIPS, W
    [J]. NATURE, 1995, 377 (6545) : 150 - 151
  • [9] A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex
    Haines, JL
    TerMinassian, M
    Bazyk, A
    Gusella, JF
    Kim, DJ
    Terwedow, H
    PericakVance, MA
    Rimmler, JB
    Haynes, CS
    Roses, AD
    Lee, A
    Shaner, B
    Menold, M
    Seboun, E
    Fitoussi, RP
    Gartioux, C
    Reyes, C
    Ribierre, F
    Gyapay, G
    Weissenbach, J
    Hauser, SL
    Goodkin, DE
    Lincoln, R
    Usuku, K
    GarciaMerino, A
    Gatto, N
    Young, S
    Oksenberg, JR
    [J]. NATURE GENETICS, 1996, 13 (04) : 469 - 471
  • [10] GENETIC-FACTORS IN MYASTHENIA-GRAVIS - A FAMILY STUDY
    KERZINSTORRAR, L
    METCALFE, RA
    DYER, PA
    KOWALSKA, G
    FERGUSON, I
    HARRIS, R
    [J]. NEUROLOGY, 1988, 38 (01) : 38 - 42