B. Oliveri
National Scientific and Technical Research Council
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Featured researches published by B. Oliveri.
Bone | 2017
C. Bondar; J. Mucci; A. Crivaro; M. Ormazabal; R. Ceci; B. Oliveri; D. González; Paula Rozenfeld
Gaucher disease (GD) is caused by mutations on the gene encoding for the lysosomal enzyme glucocerebrosidase. Type I GD (GD1) patients present anemia, hepatosplenomegaly and bone alterations. In spite of treatment, bone alterations in GD patients persist, including poor bone mineral density (BMD). Mechanisms leading to bone damage are not completely understood, but previous reports suggest that osteoclasts are involved. Chitotriosidase (CHIT) is the most reliable biomarker used in the follow up of patients, although its correlation with bone status is unknown. The aim of this work was to study the pro-osteoclastogenic potential in patients and to evaluate its correlation with CHIT activity levels and clinical parameters. PBMCs from treated patients and healthy controls were cultured in the presence of M-CSF, and mature osteoclasts were counted. BMD, blood CHIT activity and serum levels of CTX, BAP, and cytokines were evaluated in patients. We found that blood CHIT activity and osteoclast differentiation were significantly increased in patients, but no correlation between them was observed. Interestingly, osteoclast numbers but not CHIT, presented a negative correlation with BMD expressed as Z-score. CTX, BAP and serum cytokines involved in bone remodeling were found altered in GD1 patients. These results show for the first time a correlation between osteoclast differentiation and BMD in GD1 patients, supporting the involvement of osteoclasts in the bone pathology of GD1. Our results also suggest that an altered immune response may play an important role in bone damage.
Journal of Clinical Densitometry | 2016
Carlos Mautalen; Andrea Schianchi; Diego Sigal; Gisela Gianetti; Victoria Vidan; Alicia Bagur; Diana González; S.R. Mastaglia; B. Oliveri
The aim of the study was to report values for osteoporosis (OP) prevalence in Buenos Aires. Bone mineral density (BMD) at different skeletal sites was measured from November 2012 to July 2014. Participants were recruited through a newspaper advertisement inviting women at least 50 yr of age to receive free BMD measurement. After signing an informed consent form, 5448 women living in Buenos Aires and surrounding districts were studied. Lumbar spine (L1-L4), femur neck, and total hip BMDs were measured (Lunar Prodigy, software version 12.3 GE, Madison, WI, USA). OP was defined as a T-score ≤-2.5 at the lumbar spine or the femoral neck. Results showed that 1021 out of 5448 studied subjects (18.7%) had OP at the lumbar spine or the femoral neck. Comparison of age of the population sample with reference data for the general population showed a moderate (+0.6%) increase in prevalence. Prevalence of OP was low, up to the age of 70 yr when based on femoral neck BMD only. Conversely, the prevalence of OP at the lumbar spine, which was reportedly high in women up to the age of 70 yr, tended to level off over that age. The results of the total femur only added a slight (+0.7%) nonsignificant increase to the OP prevalence. A total 346,500 out of 1,853,000 women aged 50+ yr in Buenos Aires had OP at the lumbar spine or femoral neck, whereas only 163,500 had OP at the upper femur, reducing the number by 53%. The present study assessed OP prevalence in the most densely populated urban area in Argentina. The results are similar to those reported for Caucasian populations in the United States and Canada. As measurement of only the BMD of femoral neck overlooks the diagnosis in half of the women, future studies should include measurement of the lumbar spine in combination with the femoral neck for a more accurate estimation of OP prevalence.
Bone | 2006
M. Seijo; Alicia Bagur; F. Solís; Carlos Mautalen; B. Oliveri
and BMC (6, 9, and 15%, respectively). TB fat mass showed an increment of 6.7 kg (P < 0.001) mainly due to trunk fat mass (+70%). TB lean mass showed a decline of 5 kg (P < 0.05) mainly due to a diminution in peripheral lean mass: 3 kg in legs ( 16%, P < 0.0001) and 1.3 kg in arms ( 9%, P < 0.002). CONCLUSIONS: Through the decades we observed: 1—A slight (6%) diminution in DMO, with a higher diminution in area and BMC (9 and 15% respectively). 2—An increase in Total Fat Mass, predominantly in the trunk, that may have implications for the risk of cardiovascular and metabolic syndromes, and a diminution in TB lean mass, predominantly in the legs, probably related to decreased physical activity and hormonal changes. 3—Total and subregional BMD and BC reference values were obtained.
Rheumatology International | 2015
M.L. Brance; L.R. Brun; Susana Lioi; Ariel Sánchez; Marcelo Abdala; B. Oliveri
Nutricion Hospitalaria | 2013
Graciela Mabel Brito; S.R. Mastaglia; Celeste Goedelmann; Mariana Seijo; Julia Isabel Somoza; B. Oliveri
Bone | 2016
S.R. Mastaglia; Alicia Bagur; B. Oliveri; Carlos Mautalen
Bone | 2016
Carlos Mautalen; A. Schianchi; D. Sigal; G. Gianetti; V. Vidan; Alicia Bagur; Diana González; S.R. Mastaglia; B. Oliveri
Acta Bioquimica Clinica Latinoamericana | 2016
Graciela Mabel Brito; Laura Beatriz López; B. Oliveri
Bone | 2015
Graciela Mabel Brito; J. Somoza; L.B. López; B. Oliveri
Bone | 2013
M.L. Brance; L.R. Brun; J. Chiarpenello; Ariel Sánchez; M. Abdala; B. Oliveri