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Arq. NeuroPsiquiatr. vol.60 número4

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Arq Neuropsiquiat r 2002;60(4) 1051

Cam pinas. The expect at ions of t he com ponent s of 2 groups in t he beginning and in t he end of t he course w ill be evaluat ed.

In the initial part, are w oven considerations about t he medical t eaching and it s charact erist ics. It is presen-t ed brief reporpresen-t aboupresen-t presen-t he beginning of presen-t he m edical at t endance and of t he f oundat ion of t he m edical schools in Brazil. In adit t ion t o t his, it is present ed small hist ory of t he Neurology and of t he Inf ant ile Neurolo-gy in our count ry.

It is approached t he t eaching of Neurology in medi-cal graduat ion course and it is st ood out t he import an-ce of t he M edical Residenan-ce courses t o prepare quali-f ied and m odernized proquali-f essionals in t heir area oquali-f per-f orm ance per-f ront t he new know ledge in M edicine.

At t he end, t he result s of t he researchs are present ed and are w oven considerat ions relat ed t o each resear-ched segm ent .

KEY WORDS: formation and training centers in infan-tile neurology; medical residence in infaninfan-tile neurology.

ANALYSIS OF HLA DQ, DP, DR ALLELES ASSOCIATED WITH M ULTIPLE SCLEROSIS SUSCEPTIBILITY IN A POPU-LATION OF PATIENTS FROM THE RIO DE JANEIRO CITY (ABSTRACT) * DISSERTATION. NITERÓI, 2002.

CLÁUDIO CÉSAR CIRNE SANTOS * *

* Ensino da neurologia infant il no Brasil: aspect os at uais, desafios e perspect ivas (Resumo). Tese de Dout orado, Universidade Est adual de São Paulo (UNICAM P) (Área: Neurologia). Orient adora: Sylvia M aria Ciasca

* * Address: Avenida Salvador M arkow icz, 650 / 16, 12916-400 Bragança Paulist a SP, Brasil.

M ultiple sclerosis (M S) is a chronic inflammatory dise-ase of t he hum an cent ral nervous syst em of put at ively autoimmune origin characterized by multifocal demyeli-nat ion. Genet ic and environment al fact ors are t hought t o be involved in t he pat hogenesis of M S, w it h t he dis-ease considered rare in t ropical count ries, including Brazil. Genet ic st udies indicat e t hat t he major hist ocom-pat ibilit y complex (M HC)/HLA region on chromosome 6p21 cont ains M Spredisposing component (s). How -ever, w hich gene(s) present in t his region are respon-sible f or M S suscept ibilit y in t he brazilian populat ion is st ill an unset t led issue.

This st udy aim ed t o analyze t he frequencies of HLA class II alleles (DQA1* 0102, DQB1* 0602, DPA1* 0301, DRB1* 1501, DRB1* 1503) expression in a group of M S pat ient s from t he Rio de Janeiro cit y. It w as included 42 individuals (73.8% female and 26.2% male) w it h clinically definit e M S w it h age range of 15 t o 55 years. In relat ion t o et hnic background, M S pat ient s w ere of w hit e/caucasian (CA) descendent (76.2%) and (23.8%) black/african-brazilian (AF) descendent . Age-mat ched (16 t o 58 years) cont rol healt hy individuals, consist ed of 53.6% (female) and 46.4% (male) w it h t he follow -ing et hnic background: 58.3% w hit e/caucasian descen-dent and 41.7% black/african-brazilian descendescen-dent. HLA

t yping w as performed by amplificat ion of t he DNA iso-lat ed from peripheral leukocyt es w it h Polymerase Chain React ion (PCR) follow ed by SSOP hybridizat ion.

M S pat ient s show ed a posit ive associat ion for alle-les DQB1* 0602 (Pc= 0.021; RR= 2.40) and DQA1* 0102 (Pc= 0.0041; RR= 3.30). Likew ise, increased frequen-cies of DQB1* 0602 (45.2%) and DQA1* 0102 (35.7%) endow ed st rong correlat ion of t his allele com binat ion w it h disease suscept ibilit y in CA pat ient s. DR2 haplo-t ype frequencies am ong healhaplo-t hy individuals and M S group w as low. Since bot h (CA, AF) et hnic groups of M S patients show ed very low frequencies of DRB1* 1501 and DRB1* 1503 it is suggest ed t hat anot her DRB allele associat ion m ay be conferring suscept ibilit y t o M S in t his populat ion. Finally t he low frequency (RR= 0.36) of DPA1* 0301 allele consist ent ly observed in our M S pat ient s but not in t he cont rol group, indicat e t hat such allele m ay rat her have a prot ect ive role against M S.

In conclusion, genet ic suscept ibilit y t o M S in brazi-lian individuals m ay depend upon a specific allele m o-saic int eract ing at several loci necessary t o reach a crit i-cal t hreshold f or disease developm ent .

KEY W ORDS: m ult iple sclerosis, HLA, aut oim m une disease, dem yelinat ion

* Análise de alelos HLA DQ, DP, DR associados à suscet ibilidade à esclerose múlt ipla numa população de pacient es da cidade do Rio de Janeiro (Resumo). Dissert ação de M est rado, Universidade Federal Fluminense (UFF) (Área: Biologia Celular e M olecular). Orient adoras: Izabel Christ ina P. Frugulhet t i & Thereza Quírico-Sant os. Consult oria: Soniza Vieira Alves-Leon. Financial support : CAPES, CNPq

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