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1.
Nutr J ; 8: 36, 2009 Aug 10.
Article in English | MEDLINE | ID: mdl-19664270

ABSTRACT

BACKGROUND: Multiple sclerosis is a neurodegenerative disorder with a wide range in disease course severity. Many factors seem to be implicated in multiple sclerosis disease course, and diet has been suggested to play a role. Because limited data is present in the literature it was investigated whether variations in dietary intake may be related to the severity of the disease course in multiple sclerosis. METHODS: Using a food diary during 14 days, the dietary intake of 23 nutrients and vitamins was measured in patients with primary progressive (n = 21), secondary progressive (n = 32), and benign multiple sclerosis (n = 27) and compared to each other. The intake measured was also compared to the intake of the Dutch population and to the recommended daily allowance. RESULTS: Compared to the other MS groups, the secondary progressive MS patients had a lower intake of magnesium, calcium and iron. The total group of MS patients had, compared to the Dutch population, a lower intake of folate, magnesium and copper and a lower energy intake. Compared to the daily recommended allowance, the MS patients had a lower than recommended intake of folic acid, magnesium, zinc and selenium. CONCLUSION: Magnesium, calcium and iron intake may possibly be related to MS disease progression, and should receive further attention. This is important because no effective neuroprotective treatment for MS patients is available.


Subject(s)
Diet , Multiple Sclerosis/physiopathology , Adult , Calcium, Dietary/administration & dosage , Diet Records , Disease Progression , Energy Intake , Feeding Behavior , Female , Folic Acid/administration & dosage , Humans , Iron, Dietary , Magnesium/administration & dosage , Male , Middle Aged
2.
J Neurol Sci ; 244(1-2): 123-6, 2006 May 15.
Article in English | MEDLINE | ID: mdl-16519904

ABSTRACT

BACKGROUND: There is no good explanation why a proportion of patients with multiple sclerosis (MS) have a relatively benign form of the disease. An imbalance between saturated and unsaturated fatty acids (FA) might influence the disease course of MS. AIM: To assess whether the erythrocyte membrane fatty acid composition, which is a biological marker of long term dietary FA consumption, is different between patients with benign and progressive MS. METHODS: The erythrocyte membrane FA composition was measured by gas chromatography in 23 healthy controls, 27 patients with benign MS, 32 patients with secondary progressive MS and 23 patients with primary progressive MS. None of the patients was following a special diet. RESULTS: No significant differences in levels of saturated and unsaturated FA or in omega-3- and omega-6-polyunsaturated FA were found between controls and patients with the different subtypes of MS. CONCLUSION: Our data suggest that factors other than dietary fatty acid consumption are responsible for the different disease courses of MS.


Subject(s)
Dietary Fats/metabolism , Erythrocytes/metabolism , Fatty Acids/metabolism , Membrane Lipids/metabolism , Multiple Sclerosis, Chronic Progressive/blood , Multiple Sclerosis, Chronic Progressive/physiopathology , Adult , Aged , Diagnosis, Differential , Disease Progression , Fatty Acids, Unsaturated/metabolism , Feeding Behavior/physiology , Female , Humans , Male , Middle Aged
3.
J Neurol ; 253(4): 483-7, 2006 Apr.
Article in English | MEDLINE | ID: mdl-16283096

ABSTRACT

BACKGROUND: The role of oxidative stress in patients with multiple sclerosis (MS) is poorly understood. OBJECTIVE: To investigate oxidative stress in serum and peripheral blood leukocytes in patients with different disease courses of MS. METHODS: Diene conjugate (DC) levels (a measure of lipid peroxidation), total antioxidative activity (AOA) and total antiradical activity (ARA) were measured in serum and peripheral blood leukocytes from 30 patients with benign relapsing remitting MS (BMS), 27 with secondary progressive MS (SPMS), 29 with primary progressive MS (PPMS), and 30 healthy controls. All MS patients were in a clinically stable phase. RESULTS: Serum DC levels were elevated in patients with BMS (p <0.05), SPMS (p <0.01) and PPMS (p <0.001). Serum total AOA and ARA were not different between MS patients and controls. Compared to controls, leukocyte DC levels were not different in each MS subgroup, but total ARA was elevated. There was a strong correlation, both in controls and MS patients, between leukocyte DC levels and leukocyte total ARA (p <0.0001) and leukocyte total AOA (p <0.0001). CONCLUSION: Oxidative stress occurs in progressive as well as benign MS. The finding that cells withstand oxidative stress, due to upregulated cellular antioxidant defence mechanisms, suggests that reactive oxygen species (ROS) formation in MS is not necessarily deleterious.


Subject(s)
Leukocytes/metabolism , Multiple Sclerosis/blood , Oxidative Stress/physiology , Adult , Aged , Antioxidants/metabolism , Disease Progression , Female , Free Radical Scavengers/metabolism , Humans , Hydrogen Peroxide/blood , Interferons/therapeutic use , Leukocyte Count , Lipid Peroxidation/physiology , Male , Middle Aged , Multiple Sclerosis/drug therapy
4.
J Neurol Sci ; 231(1-2): 41-4, 2005 Apr 15.
Article in English | MEDLINE | ID: mdl-15792819

ABSTRACT

BACKGROUND: A number of studies found that patients with multiple sclerosis (MS) have low serum levels of uric acid. It is unclear whether this represents a primary deficit or secondary effect. Uric acid is a scavenger of peroxynitrite, which is the product of nitric oxide (NO) and superoxide. Because peripheral blood leukocyte NO production and NO metabolites in serum are raised in MS patients, associations might be expected between serum uric acid levels and peripheral NO production. METHODS: Serum levels of uric acid and NO production by peripheral blood leukocytes were measured in 60 patients with MS without a relapse in the past 3 months, and 30 age- and sex-matched healthy controls. Uric acid was determined with the uricase PAP method, and NO production was assayed by measuring nitrite concentration in supernatants of lysed leukocytes. RESULTS: Serum uric acid levels were not different between MS patients and controls. Compared to controls, patients with MS had significantly higher peripheral blood leukocytes nitrite concentrations (p<0.001). There was no correlation between leukocyte nitrite concentration and serum uric acid levels. CONCLUSIONS: Our findings suggest that in MS patients there is no primary deficit in serum uric acid. NO production by peripheral blood leukocytes is increased, but there is no association with serum uric acid levels.


Subject(s)
Leukocytes/metabolism , Multiple Sclerosis/blood , Nitric Oxide/metabolism , Uric Acid/blood , Adult , Case-Control Studies , Female , Humans , Interferon-beta/therapeutic use , Leukocytes/drug effects , Male , Middle Aged , Multiple Sclerosis/drug therapy , Multiple Sclerosis/metabolism , Reference Values , Statistics, Nonparametric
5.
Neurology ; 62(2): 239-42, 2004 Jan 27.
Article in English | MEDLINE | ID: mdl-14745060

ABSTRACT

BACKGROUND: Nitric oxide (NO) may play a role in tissue destruction and axonal degeneration in multiple sclerosis (MS). OBJECTIVE: To investigate NO production by peripheral blood leukocytes (PBL) in patients with a benign and progressive course of MS. METHODS: PBL were isolated from 25 patients with a benign course of MS (BMS), 33 with secondary progressive MS (SPMS), 21 with primary progressive MS (PPMS), and 29 healthy individuals. Leukocyte supernatants were assayed for nitrite concentration, which is an index of NO generation, using the Griess reaction. Serum levels of tumor necrosis factor (TNF)alpha and interleukin (IL)-12 were measured using ELISA. RESULTS: Compared to healthy controls, nitrite concentrations were higher in patients with BMS (p < 0.001), SPMS (p < 0.001), and PPMS (p < 0.05). There were no significant differences among the three clinical subgroups of MS. There was a correlation between nitrite concentrations and serum levels of IL-12 (p = 0.04), but not of TNFalpha. CONCLUSION: Increased NO production by PBL in patients with MS is independent of the disease course.


Subject(s)
Leukocytes/metabolism , Multiple Sclerosis/blood , Nitric Oxide/blood , Adult , Axons/pathology , Female , Humans , Interleukin-12/blood , Male , Middle Aged , Multiple Sclerosis/classification , Multiple Sclerosis, Chronic Progressive/blood , Nerve Degeneration , Nitrites/blood , Tumor Necrosis Factor-alpha/analysis
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