[Palmar fasciitis arthritis syndrome revealing relapse of chronic lymphoid leukemia].
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Biomedical subjects
Publications and source records attributed to S Rozenberg.
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In this cross-sectional study, the relative importance of anthropometric factors and that of biological parameters on bone mineralization were evaluated and their practical implications inferred on the choice of the parameter to be used for the estimation of bone mineralization. A close relationship between anthropometric factors and bone mineral content (BMC) was observed and this relationship was shown to be independent of age. Furthermore, by regression analyses, anthropometric parameters appeared to explain a large part of the variance in BMC and preceded the hormonal parameters in the stepwise analysis of this model. Using bone mineral density (BMD) data, however, we observed a weaker relationship between anthropometric factors and bone mineralization and a relatively stronger relationship between steroid hormones and bone mineralization than those observed using the BMC data. Furthermore, by multiple regression analysis the hormonal factors preceded the anthropometric parameters in the stepwise analysis of the model. As strong epidemiological and clinical evidence exists on the relationship between steroid hormones and bone loss, these results constitute a supplementary argument for the use of BMD for the estimation of bone mineralization.
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We describe a case of spondylodiscitis caused by Campylobacter fetus in a previously healthy patient. This is the first report of this agent causing discovertebral infection, which generated cellular immune deficiency, reversible with the cure.
After 5, 16 and 21 years of occupational exposure to silica, 2 men and 1 woman, respectively, were diagnosed as having dermatopolymyositis. Pulmonary impairment was always present and took the form of diffuse interstitial fibrosis in 2 patients, whose lung biopsies revealed high particulate silica contents. The role of silica in the induction of dermatopolymyositis is discussed in light of published information on silica-induced connective tissue diseases.
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The possible existence of correlations between bone mineral content (BMC), age and serum levels of steroid hormones was investigated. It was found that dehydroepiandrosterone sulphate (DHEA-S), oestradiol (E2) and delta-4-androstenedione (A) were correlated with BMC, whereas oestrone (E1) and testosterone (T) were not. Partial correlations after adjustment for age were significant (P less than 0.05) only between E2 and DHEA-S and BMC at the L2-L4 lumbar site (BMC-1) and between DHEA-S (P less than 0.01) and BMC at the midradius site (BMC-r). Stepwise multiple regression analysis showed that, apart from age, E2 was the only factor to fit (P less than 0.05) into the mathematical model with BMC-1 as the dependent variable, while DHEA-S was the only factor to fit (P less than 0.01) with BMC-r as the dependent variable. These data suggest that different hormonal influences are related to BMC at different sites, namely E2 to lumbar trabecular bone (L2-L4) and DHEA-S to cortical bone (midradius).
Abnormal bone metabolism was reported in rheumatoid arthritis (RA). In order to evaluate the interest of serum osteocalcin, also called bone GLA-protein (BGP), to assess bone metabolism in RA, we studied 20 postmenopausal RA out-patients and 20 matched controls. Nine patients were treated with low-dose corticosteroids (C+) for at least one year (less than 10 mg/day, prednisolone equivalent), the remaining 11 (C-) received non-steroidal anti-inflammatory drugs (NSAID). The distal and proximal forearm bone mineral content (BMC) was measured by single photon absorptiometry, the vertebral BMC was measured by dual photon absorptiometry. A trend to low BGP was observed in the C+ group. The lowest values were observed in patients with vertebral fractures. Compared with controls, both RA groups had similar low significant BMC at the forearm sites. At the vertebral sites, the bone mineral content decrease observed in the two groups, was more marked in the C+ group. From our results, BGP did not appear as a useful index of osteoporosis in RA, except in some patients with vertebral fractures, treated with low-dose corticosteroids.
Osteoporosis, an important health problem, essentially concerns postmenopausal women since women have a lower peak bone mass than men when they reach adulthood and since the menopause is associated with an accelerated bone loss. We retrospectively analysed the bone measurements of 318 women, age less than 50. The bone mineral contents and densities of the mid- and distal radius (BMC m-rad, BMD m-rad, BMC d-rad, BMD d-rad) and of the lumbar L2-L4 vertebra (BMC L2-L4, BMD L2-L4) were measured using single and dual photon absorptiometer, respectively. The relations between age, height, weight, body mass index and the bone measurements were studied using multiple regression analyses. The anthropometric factors were accepted as first factors in the equations. R2 were respectively 17%, 17%, 28% for BMC m-rad, BMC d-rad, BMC L2-L4 and 7%, 5%, 8% for BMD m-rad, BMD d-rad, BMD L2-L4. These data suggest that anthropometric factors have an important influence on the different bone measurements. They also draw attention on the importance of preventive measures to achieve and to maintain an optimal bone reserve in premenopausal women.
Serum osteocalcin was measured in patients receiving corticosteroid for long and short term at different doses. Low osteocalcin levels were observed in treated patients compared to age and sex matched controls (p less than 0.001). The effect was dose dependent and paralleled the adrenal inhibition assessed by morning cortisol. Short term administration resulted in a rapid decline of baseline osteocalcin which was maintained during the treatment period and was reversible after withdrawal. Osteocalcin appeared as a sensitive index of the inhibitory effect of corticosteroid on osteoblasts.
Changes in the serum levels of gonadotrophins and steroid hormones with increasing age were studied in 449 women aged 40 and over to investigate the relationships between these hormones even very late in life. The levels of oestradiol (E2) and dehydroepiandrosterone sulphate (DHEA-S) fell after age 50 and remained low thereafter. However, while serum oestrone (E1), testosterone (T), delta-4-androstenedione (A) and prolactin (PRL) concentrations also decreased initially after age 50 they subsequently rose again progressively and this increase was in fact significant in the case of E1. Luteinizing hormone (LH) and follicle-stimulating hormone (FSH) rose after age 50, but whereas FSH remained elevated, LH decreased late in life. Cortisol (F) increased significantly after age 70. There was a significant correlation between androgens and E1 as well as between E2 and LH, even after age 60. Owing to the great heterogeneity of the population studied, it is not yet possible to speculate as to the physiopathological significance of these observations. It would seem, however, that the negative feedback effect of oestrogens on LH secretion remains operational very late in life.
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