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1.
Ann Rheum Dis ; 75(5): 879-82, 2016 May.
Article in English | MEDLINE | ID: mdl-26458738

ABSTRACT

OBJECTIVE: Ankylosing spondylitis (AS) is a chronic inflammatory disease affecting the spine and pelvis of young adults. On the HLA-B27 genetic background, the occurrence of AS is influenced by the intestinal microbiota. The goal of our study was to test whether breast feeding, which influences microbiota, can prevent the development of AS. METHODS: First, 203 patients with HLA-B27-positive AS fulfilling the modified New York criteria were recruited in the Department of Rheumatology, Ste Marguerite hospital in Marseilles. A total of 293 healthy siblings were also recruited to make up a control group within the same families. Second, 280 healthy controls, and 100 patients with rheumatoid arthritis and their siblings were recruited. The data collected were age, gender, number of brothers and sisters, age at disease onset, type and duration of feeding (breast or bottle). RESULTS: Patients with AS had been breast fed less often than healthy controls. In families where children were breast fed, the patients with AS were less often breast fed than their healthy siblings (57% vs 72%), giving an OR for AS onset of 0.53 (95% CI (0.36 to 0.77), p value=0.0009). Breast feeding reduced familial prevalence of AS. The frequency of breast feeding was similar in the AS siblings and in the 280 unrelated controls. However, patients with AS were less often breast fed compared with the 280 unrelated controls (OR 0.6, 95% CI (0.42 to 0.89), p<0.01). CONCLUSIONS: Our study suggests a breastfeeding-induced protective effect on the occurrence of AS. To our knowledge, this is the first study of breastfeeding history in patients with AS.


Subject(s)
Breast Feeding/statistics & numerical data , Spondylitis, Ankylosing/prevention & control , Adolescent , Adult , Aged , Aged, 80 and over , Arthritis, Rheumatoid/prevention & control , Bottle Feeding/statistics & numerical data , Female , Gastrointestinal Microbiome , Genetic Predisposition to Disease , HLA-B27 Antigen/genetics , Humans , Male , Middle Aged , Retrospective Studies , Siblings , Spondylitis, Ankylosing/genetics , Spondylitis, Ankylosing/microbiology , Time Factors , Young Adult
2.
Arthritis Rheum ; 60(1): 73-80, 2009 Jan.
Article in English | MEDLINE | ID: mdl-19117368

ABSTRACT

OBJECTIVE: Rheumatoid arthritis (RA) is an autoimmune disease that affects mostly women and is associated with HLA-DRB1 genes having in common a shared epitope sequence. In parallel, cells and/or DNA originating from pregnancy (microchimerism) persist for decades and could contribute to autoimmunity. The aim of this study was to examine whether microchimerism may be a source of the shared epitope among women with RA. METHODS: Women with RA and healthy women who lacked RA-associated genes such as HLA-DRB1*01 (n=33 and n=46, respectively) and/or HLA-DRB1*04 (n=48 and n=64, respectively), were tested for DRB1*01 or DRB1*04 microchimerism by HLA-specific quantitative polymerase chain reaction assays. As controls, alleles not associated with RA (DQB1*02 and DRB1*15/16) were also analyzed. RESULTS: Compared with healthy women, women (42% with RA had a higher frequency and higher levels of DRB1*04 microchimerism versus 8%; P=0.00002) as well as DRB1*01 microchimerism (30% versus 4%; P=0.0015). Moreover, no difference in microchimerism was observed for alleles not associated with RA. CONCLUSION: Women with RA had microchimerism with RA-associated HLA alleles, but not with non-RA-associated HLA alleles, more often and at higher levels compared with healthy women. These observations are the first to indicate that microchimerism can contribute to the risk of an autoimmune disease by providing HLA susceptibility alleles.


Subject(s)
Arthritis, Rheumatoid/genetics , Chimerism , Epitopes/genetics , HLA-DQ Antigens/genetics , HLA-DR Antigens/genetics , Maternal-Fetal Exchange/genetics , Arthritis, Rheumatoid/epidemiology , Female , Genotype , HLA-DQ beta-Chains , HLA-DRB1 Chains , Humans , Mothers , Pregnancy , Risk Factors
3.
Prosthet Orthot Int ; 30(1): 87-96, 2006 Apr.
Article in English | MEDLINE | ID: mdl-16739785

ABSTRACT

The aim of this study was to assess the extent to which orthopaedic shoes improved gait in a patient with Charcot-Marie-Tooth (CMT) disease and to show how the latest gait analysis tools available can help to assess and quantify the efficacy of this treatment. The case of a 55-year-old woman with CMT disease is described. She complained mainly of pain and frequent falling. The physical examination and the clinical gait analysis showed the presence of bilateral foot drop, high-stepping and varus. Treatment based on physical therapy and orthopaedic shoes was prescribed. In order to assess the clinical efficacy of the treatment, a complete physical examination was carried out after the patient had been wearing the orthopaedic shoes for one month. The quantified assessment was performed with a Gaitrite system, which can be used to record the spatio-temporal parameters of gait. It was concluded that orthopaedic shoes provide specialists in physical and rehabilitation medicine with an excellent means of treating gait disabilities in patients with CMT disease. With the made-to-measure orthopaedic shoes used, the falling and pain disappeared; the patient's walking speed increased and the foot support base decreased in size. Both the clinical and quantified data confirmed the subjective improvement perceived by the patient. The latest tools available for performing quantified gait analysis in clinical practice provide useful means of objectively assessing the success of treatment.


Subject(s)
Charcot-Marie-Tooth Disease/complications , Gait Disorders, Neurologic/etiology , Gait Disorders, Neurologic/therapy , Orthotic Devices , Shoes , Charcot-Marie-Tooth Disease/physiopathology , Female , Gait Disorders, Neurologic/physiopathology , Humans , Middle Aged , Treatment Outcome
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