Genetic markers in rheumatoid arthritis
1985 (English)Doctoral thesis, comprehensive summary (Other academic)
Genetic as well as environmental factors are believed to be of importance in the etiology of rheumatoid arthritis (RA). There are a number of previous studies of genetic markers in RA, but so far no genetic linkage and only a few associations have been found. Of the associations only one (with the HLA antigen DR4) appears to be well documented. In most previous association studies the patients have not been divided according to sex and family history of RA.
In this investigation the HLA antigens A, B and DR and five serum protein systems (Bf, C3, Pi, Hp and Tf) were studied in patients with erosive rheumatoid arthritis (RA), from northern Sweden. Special attention was paid to variations in the strength of associations according to sex and family history of polyarthritis. The following results were found:
The frequency of the HLA antigen B27 was significantly increased in the North-Swedish population (16.6%) and among patients with a family history of polyarthritis (42.6%). In agreement with previous investigations a significantly increased frequency of the DR4 antigen was found in the RA patients.
In the properdin factor B (Bf) system the S phenotype was found to be significantly increased in male patients and in patients with a family history of polyarthritis, more severe form of RA and high titres of rheumatoid factor.
No significant differences with respect to phenotype or gene frequencies were found in the C3 complement system. Thus, the association between RA and C3 found in previous investigations was not confirmed.
A significant increase of rare alpha-1-antitrypsin (Pi) types (MS, MZ, MF and SZ) was found among RA patients. However, the increase concerned mainly Z heterozygotes and was more strongly pronounced among male patients.
In the haptoglobin system a significant increase of the Hp^ gene and the Hp2-2 type was found among patients with a family history of polyarthritis, more pronounced among males.
A significant increase of the transferrin gene and of the 2 type was found among male RA patients, more pronounced among patients with a family history of polyarthritis.
In 6 out of 8 gene loci studied significant associations were found, which is in agreement with a multifactorial etiology of RA. The results were largely in agreement with the hypothesis that associations would be expected to be stronger in males and in patients with a family history of polyarthritis. A notable finding was the high frequency of first degree relatives (around 40%) with symmetric peripheral polyarthritis of which more than 70% had a diagnosis of RA verified by hospital records.
Place, publisher, year, edition, pages
Umeå: Umeå universitet , 1985. , 29 p.
Umeå University medical dissertations, ISSN 0346-6612 ; 151
Rheumatoid arthritis, family history, genetic marker, HLA B27, HLA DR4, properdin factor B, C3 complement, -antitrypsin, haptoglobin, transferrin
Rheumatology and Autoimmunity
IdentifiersURN: urn:nbn:se:umu:diva-101305OAI: oai:DiVA.org:umu-101305DiVA: diva2:799846
1985-09-27, Sal B, 9 tr, Tandläkarhögskolan, Umeå universitet, Umeå, 09:15
Diss. (sammanfattning) Umeå : Umeå universitet, 1985, härtill 6 uppsatser.2015-04-212015-03-262015-04-21Bibliographically approved