2005: Clinical characteristics of African Americans vs Caucasian Americans with multiple sclerosis. 
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 2005: Clinical characteristics of African Americans vs Caucasian Americans with multiple sclerosis.

1: Neurology. 2004 Dec 14;63(11):2039-45.  Links
Comment in:
Neurology. 2005 Jun 28;64(12):2163.
Clinical characteristics of African Americans vs Caucasian Americans
with multiple sclerosis.
Cree BA, Khan O, Bourdette D, Goodin DS, Cohen JA, Marrie RA, Glidden
D, Weinstock-Guttman B, Reich D, Patterson N, Haines JL, Pericak-Vance
M, DeLoa C, Oksenberg JR, Hauser SL.
Multiple Sclerosis Center, Department of Neurology, University of
California San Francisco, 350 Parnassus Ave., Suite 908, San Francisco,

BACKGROUND: African American (AA) individuals are thought to develop
multiple sclerosis (MS) less frequently than Caucasian American (CA)
individuals. OBJECTIVE: To compare the clinical characteristics of AA
and CA patients with MS. METHODS: The clinical features of MS were
compared in a large retrospective cohort of AA (n = 375) and CA (n =
427) subjects. RESULTS: The proportion of women to men was similar in
AA and CA subjects (81% [AA] vs 77% [CA]; p = 0.122). There were no
differences in the proportions of subjects with relapsing-remitting,
secondary progressive, primary progressive, and progressive relapsing
MS. The median time to diagnosis was 1 year after symptom onset in AA
subjects and 2 years after symptom onset in CA subjects (p = 0.0013).
The age at onset was approximately 2.5 years later in AA than CA
subjects (33.7 vs 31.1 years; p = 0.0001). AA subjects presented with
multisite signs and symptoms at disease onset more often than CA
subjects (p = 0.018). Clinical involvement restricted to the optic
nerves and spinal cord (opticospinal MS) occurred in 16.8% of AA
patients compared with 7.9% of CA patients (p < 0.001). Transverse
myelitis also occurred more frequently in AA subjects (28 vs 18%; p =
0.001). Survival analysis revealed that AA subjects were at higher risk
for development of ambulatory disability than CA subjects. After
adjusting for baseline variations and differences in therapeutic
interventions, AAs were at 1.67-fold greater risk for requiring a cane
to ambulate than CA patients (p < 0.001). There was a trend suggesting
that AAs were also at greater risk for development of wheelchair
dependency (p = 0.099). Adjusted Cox proportional hazard models showed
that this effect was in part attributable to the older age at onset in
AAs (p < 0.001). CONCLUSIONS: Compared with multiple sclerosis (MS) in
Caucasian Americans, African American patients with MS have a greater
likelihood of developing opticospinal MS and transverse myelitis and
have a more aggressive disease course.

PMID: 15596747 [PubMed - indexed for MEDLINE]



Tue, 30 Jun 2009 00:43:25 GMT
 2005: Clinical characteristics of African Americans vs Caucasian Americans with multiple sclerosis.


Fri, 19 Jun 1992 00:00:00 GMT
 2005: Clinical characteristics of African Americans vs Caucasian Americans with multiple sclerosis.

Quote:

> 1: Neurology. 2004 Dec 14;63(11):2039-45.  Links
> Comment in:
> Neurology. 2005 Jun 28;64(12):2163.
> Clinical characteristics of African Americans vs Caucasian Americans
> with multiple sclerosis.
> Cree BA, Khan O, Bourdette D, Goodin DS, Cohen JA, Marrie RA, Glidden
> D, Weinstock-Guttman B, Reich D, Patterson N, Haines JL, Pericak-Vance
> M, DeLoa C, Oksenberg JR, Hauser SL.
> Multiple Sclerosis Center, Department of Neurology, University of
> California San Francisco, 350 Parnassus Ave., Suite 908, San Francisco,

> BACKGROUND: African American (AA) individuals are thought to develop
> multiple sclerosis (MS) less frequently than Caucasian American (CA)
> individuals. OBJECTIVE: To compare the clinical characteristics of AA
> and CA patients with MS. METHODS: The clinical features of MS were
> compared in a large retrospective cohort of AA (n = 375) and CA (n =
> 427) subjects. RESULTS: The proportion of women to men was similar in
> AA and CA subjects (81% [AA] vs 77% [CA]; p = 0.122). There were no
> differences in the proportions of subjects with relapsing-remitting,
> secondary progressive, primary progressive, and progressive relapsing
> MS. The median time to diagnosis was 1 year after symptom onset in AA
> subjects and 2 years after symptom onset in CA subjects (p = 0.0013).
> The age at onset was approximately 2.5 years later in AA than CA
> subjects (33.7 vs 31.1 years; p = 0.0001). AA subjects presented with
> multisite signs and symptoms at disease onset more often than CA
> subjects (p = 0.018). Clinical involvement restricted to the optic
> nerves and spinal cord (opticospinal MS) occurred in 16.8% of AA
> patients compared with 7.9% of CA patients (p < 0.001). Transverse
> myelitis also occurred more frequently in AA subjects (28 vs 18%; p =
> 0.001). Survival analysis revealed that AA subjects were at higher risk
> for development of ambulatory disability than CA subjects. After
> adjusting for baseline variations and differences in therapeutic
> interventions, AAs were at 1.67-fold greater risk for requiring a cane
> to ambulate than CA patients (p < 0.001). There was a trend suggesting
> that AAs were also at greater risk for development of wheelchair
> dependency (p = 0.099). Adjusted Cox proportional hazard models showed
> that this effect was in part attributable to the older age at onset in
> AAs (p < 0.001). CONCLUSIONS: Compared with multiple sclerosis (MS) in
> Caucasian Americans, African American patients with MS have a greater
> likelihood of developing opticospinal MS and transverse myelitis and
> have a more aggressive disease course.

> PMID: 15596747 [PubMed - indexed for MEDLINE]

OT -  MS info

Intresting though, does someone have MS in your family?



Tue, 30 Jun 2009 01:46:23 GMT
 
 [ 3 post ] 

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