Guido Zarattini

Loss of sight and sound. Could it be the hip

In September, 2007, a 58-year-old woman was admitted to our neurology department because of progressive visual and hearing loss which had started 9 months earlier. She had type 2 diabetes and hypertension, both of which were adequately controlled by medication. In 2001, she had a left hip arthroplasty which was revised in October, 2006 because of rupture of the ceramic head. 3 weeks before admission, investigations showed a mild hypothyroidism of unknown origin, which was treated with levothyroxine sodium. The neurological examination at admission showed impairment of cranial nerves II and VIII bilaterally and mild distal sensory-motor dis turbances. Laboratory investigations ruled out haema tological, infectious, neoplastic, metabolic, and immuno logical diseases. Concomitantly our patient underwent various investigations including brain MRI (showing hyperintensity of optic nerves and tracts), electromyography (showing mild lower limb nerve amplitude reduction), and acoustic and visual evoked potentials (positive for bilateral absence of brainstem acoustic responses and irregular cortical visual responses). A working diagnosis of axonal multi-neuropathy caused by a presumed immune-mediated vasculitis was made and the patient was given prednisone (50 mg/day) for 2 months with little improvement. By December, 2007, our patient became completely blind, severely deaf, and wheel-chair bound because of lower limb hyposthenia. Tests for immune-mediated process remained negative and the case was referred to toxicology for further investigation. Unexpectedly, raised concentrations of cobalt and chromium were found in diff erent biological samples (cobalt: 24 h urine collection 1187 μg/L [0·1–1·5], blood 549 μg/L [0·05–2·7], plasma 90 μg/L [0·1–0·6], CSF 11·4 μg [0·05–0·15]; chromium: 24 h urine collection 510 μg/L [0·05–2·2], blood 54 μg/L [0·1–0·5], plasma 210 μg/L [0·1–0·5], CSF 4·4 μg/L [0·01–0·2]). Cobalt-chromium poisoning due to metal wear debris from her hip prosthesis was proposed, although radiology, including CT, showed no sign of prosthesis loosening. In February, 2008, several metal ion chelating treatments were given with edetic acid. Although metal ion concentrations decreased, neurological improve ment was negligible. Therefore, in April, 2008, resection arthroplasty was done. During surgery infi ltration of the peri-prosthesic tissue by metallic debris was evident (fi gure A); analysis of peri-prosthetic fl uids showed high concentrations of cobalt and chromium, and the removed prosthesis showed wear of the head and neck (fi gure B), supporting the hypothesis of endogenous cobalt-chromium poisoning. During the following 8 months the patient showed progressive improvement, although vision only partially improved. Metal ion concentrations decreased but remained higher than reference values at the last follow-up in November, 2008. The role of cobalt or cobalt-chromium on human tissues has not been defi nitively established. Cobalt can produce various toxicological eff ects including local respiratory symptoms due to inhalation of cobalt containing dusts, and systemic eff ects (thyroiditis, cardiomyopathy, erythropoiesis). Neuro logical toxicity, mainly optic atrophy, nerve deafness, and limb paraesthesia, has been occasionally reported in association with exogenous exposure. Neuro logical toxicity as a reult of endogenous exposure (mainly associated with metal prostheses) has been described. Cobalt can induce a hypoxia-like eff ect, possibly targeting mitochondria; of note, our patient’s symptoms were similar to those observed in some mitochondrial cytopathies. Total hip replacement and hip resurfacing arthroplasty are widely used therapeutic procedures; longer-term follow-up would be necessary to evaluate adverse chronic systemic eff ects due to prolonged exposure to high serum cobalt concentrations. In addition to orthopaedic evaluation, careful neurological and toxicological examinations are recommended whenever a patient with a metallic prosthesis complains of visual loss, hearing disturbance, limb weakness, numbness, or paraesthesia, even in the absence of local osteoarticular symptoms.

Cobalt, chromium and molybdenum ions kinetics in the human body: data gained from a total hip replacement with massive third body wear of the head and neuropathy by cobalt intoxication

IntroductionA patient with a total hip replacement developed optic, acoustic and peripheral neuropathy from metal ions intoxication, due to the wear products released from the prosthesis. Subsequently the kinetics of the metal ions was studied.Materials and methodsMassive wear and acute intoxication allowed a study of the metal ions kinetics and of EDTA treatment.ResultsPlasma and other organic fluids were saturated by each of the metal ions released from the exposed surface according to the solubility of each ion; a larger fraction of Co ions was bound within red cells, while the plasmatic fraction appeared more movable. In a patient with a prosthesis subjected to wear, the ions released are from the prosthetic and from the debris surface (spread in the body). The latter is a function of the number and size of particles.DiscussionRevision of the prosthesis from the point of view of the metal ions kinetics corresponded to a reduction of the releasing surface because of debris washed out by irrigation and tissue excision; however, the metal particles spread by lymphatic circulation continued to release ions even though the source of wear had been removed. Early diagnosis of high metal wear can be ascertained with mass spectrometry and after revision high levels of metal ions can only be reduced with repeated chelating treatment. It is preferable not to revise fractured ceramic components with a polyethylene–metal articulation.

Morphometric Analysis of the Canal System of Cortical Bone: An Experimental Study in the Rabbit Femur Carried Out with Standard Histology and Micro‐CT

The osteonal pattern of cortical bone is gradually built around the intracortical vessels by the progression of the cutting cones (secondary remodelling); therefore, the central canal size can be used as index of the remodelling activity. An experimental model in the rabbit femur was used to investigate, through central canal morphometry and frequency distribution analysis, the remodelling activity, comparing the middle of the diaphysis (mid‐shaft) with the extremity (distal‐shaft) and at the same level sectors and layers of the cortex in transversal sections. The study documented a higher density of canals in the mid‐shaft than in the distal‐shaft and a higher remodelling in the distal‐shaft. There were no significant differences between dorsal, ventral, medial and lateral sectors at both mid‐shaft and distal‐shaft levels, while the number of canals was higher in the sub‐periosteal layers than in the sub‐endosteal. A lower threshold of 40 μm2 was observed in the central canal area. Sealed osteons in the midshaft were 22.43% of the total number of osteons of the central canal area between 40 and 200 μm2 and 0.44% of those of the distal‐shaft. Micro‐CT allowed a 3D reconstruction of the vascular canal system, which confirmed the branched network pattern rather than the trim architecture of the traditional representation. Some aspects like the lower threshold of the central canal size and the sealed osteons documented the plasticity of the system and its capacity for adaptation to changes in the haemodynamic conditions.

The surgical treatment of isolated mason type 2 fractures of the radial head in adults: comparison between radial head resection and open reduction and internal fixation.

Objectives: To compare the outcomes of two different surgical treatments for the management of isolated closed Mason Type 2 radial head fractures. Design: Retrospective study. The Student t test and McPearson chi-square test were used to evaluate whether there was a significance difference between the groups. Patients: Fifty-nine patients with isolated Mason Type 2 radial head fractures. Intervention: Twenty-four patients treated with radial head excision (Group I) and 35 treated with open reduction and internal fixation (Group II). Main Outcome Measurements: Clinical outcomes were assessed using the Broberg and Morrey functional rating scores and the Disabilities of the Arm, Shoulder and Hand (DASH) questionnaire. Orthogonal radiographs were performed on both the elbow and the wrist; these were assessed for the presence of arthritis, heterotopic ossification, and the degree of proximal radial migration. Results: The length of postoperative follow-up was 157 ± 61.84 months (Group I) and 125 ± 39.09 months (Group II). The Broberg and Morrey functional rating score was 86.21 ± 6.10 points and 95.09 ± 4.78 points, respectively. The DASH score was 21.82 ± 6.01 points and 2.81 ± 2.73 points, respectively. Radiologically moderate or severe osteoarthritis was present in the elbows of nine patients in Group I and only two patients in Group II. Conclusions: Patients with isolated Mason Type 2 radial head fractures treated by open reduction and internal fixation (Group II) had less residual pain, greater range of motion, and better strength than patients treated by radial head excision (Group I). Additionally, Group II had a lower incidence of severe posttraumatic arthritis, which contributed to improved DASH and Broberg and Morrey functional scores. These results support open reduction and internal fixation as the treatment of choice for these fractures. Level of Evidence: Therapeutic Level III. See Instructions for Authors for a complete description of levels of evidence.

A Review of the Actual Knowledge of the Processes Governing Growth and Development of Long Bones

Autoptic samples of human bones (from 8 weeks of gestation to 12 years of age) and a second group of serial, skeletal x-rays (required for pathologies not related to bone dysplasia in children from 4 months to 17 years of age) provided the material for the analysis of the physes normal growth mechanism presented in this review. Before the appearance of the ossification centers epiphyseal growth rests exclusively on chondrocytes proliferation (interstitial growth), without any detectable differentiated cellular organization. When endochondral ossification starts a defined spatial disposition of chondrocytes and a corresponding organization of the intercellular matrix is set up, so that it is possible to identify a growth vector corresponding to the columns of piled chondrocytes with direction from hypertrophic toward the proliferative cell layers. The complexity of the tubular bones growth process is well represented by the spatial arrangement of the growth vectors. In the late epiphyseal growth another mechanism is active in addition to endochondral ossification, namely, articular cartilage interstitial growth and subchondral remodelling. The knowledge of the normal mode of organization of the physis and its temporal sequence can help to better understand of the deviaton from the normal development of metaphyseal and epiphyseal dysplasias.

A model of osteoblast–osteocyte kinetics in the development of secondary osteons in rabbits

The kinetics of osteogenic cells within secondary osteons have been examined within a 2‐D model. The linear osteoblast density of the osteons and the osteocyte lacunae density were compared with other endosteal lamellar systems of different geometries. The cell density was significantly greater in the endosteal appositional zone and was always flatter than the central osteonal canals. Fully structured osteons compared with early structuring (cutting cones) did not show any significant differences in density. The osteoblast density may remain constant because some of them leave the row and become embedded within matrix. The overall shape of the Haversian system represented a geometrical restraint and it was thought to be related to osteoblast–osteocyte transformation. To test this hypothesis of an early differentiation and recruitment of the osteoblast pool which completes the lamellar structure of the osteon, the number and density of osteoblasts and osteocyte lacunae were evaluated. In the central canal area, the mean osteoblast linear density and the osteocyte lacunae planar density were not significantly different among sub‐classes (with the exclusion of the osteocyte lacunae of the 300–1000 μm2 sub‐class). The mean number of osteoblasts compared with osteocyte lacunae resulted in significantly higher numbers in the two sub‐classes, no significant difference was seen in the two middle sub‐classes with the larger canals, and there were significantly lower levels in the smallest central canal sub‐class. The TUNEL technique was used to identify the morphological features of apoptosis within osteoblasts. It was found that apoptosis occurred during the late phase of osteon formation but not in osteocytes. This suggests a regulatory role of apoptosis in balancing the osteoblast–osteocyte equilibrium within secondary osteon development. The position of the osteocytic lacunae did not correlate with the lamellar pattern and the lacunae density in osteonal radial sectors was not significantly different. These findings support the hypothesis of an early differentiation of the osteoblast pool and the independence of the fibrillar lamellation from osteoblast–osteocyte transformation.

Structural pattern and functional correlations of the long bone diaphyses intracortical vascular system: investigation carried out with China ink perfusion and multiplanar analysis in the rabbit femur.

The intracortical vessel system of the rabbit femur has been studied after perfusion of the vascular tree with a water solution of dye (China ink) with multiplanar analysis. This method utilizes the full depth of field of the microscope objectives focusing different planes of the thick cortex. The microscopic observation even if restricted to a limited volume of cortex allowed to differentiate true 3-D nodes (54.5%) from the superimposition of vessels lying on different planes. The network model with elongated meshes preferentially oriented along the longitudinal axis of the diaphysis in his static configuration is not very different from the vascular anatomy depicted in the 2-D traditional models; however, the semi-quantitative morphometric analysis applied to the former supported the notion of a multidirectional microvascular network allowing change of flow according to the functional requirements. Other peculiar aspects not previously reported were cutting cone loops, blind-end and short-radius-bent vessels, and button-holes figures. The network design and node distribution were consistent with the straight trajectory of the secondary remodeling, with the proximal-to-distal and distal-to-proximal advancement directions of the cutting cones and with two main modes of node formation, namely bifurcation of the cutting cone and interception with pre-existing canals. The general organization of the network and its uninterrupted transformation during bone modeling and remodeling suggested a substantial plasticity of the intracortical vascular system capable to adapt itself to the changeable haemodynamic conditions.

Setup of a bone aging experimental model in the rabbit comparing changes in cortical and trabecular bone: Morphological and morphometric study in the femur

Bone aging was studied in an experimental model (rabbit femur) in three populations aged 0.5, 1.5, and 7.5 years. Cortical bone histology was compared with a data set from a 1.5‐month‐old population of an earlier published paper. From 0.5‐year‐old onward, the mean femur length did not increase further. Thereafter, the mean marrow area increased and the cortical area decreased significantly with aging. This was associated with a structural pattern transformation from plexiform to laminar and then Haversian‐like type. The distal meta‐epiphysis bone trabecular density of the oldest populations also was significantly lower in specific regions of interest (ROI). Percentage sealed primary vascular canals in laminar bone significantly increased with aging without variation of percentage sealed secondary osteons. Remodeling rate reflected by the density of cutting cones did not significantly change among the age populations. These data suggest that laminar bone vascular pattern is more functional in the fast diaphyseal expansion but not much streamlined with the renewal of blood flow during secondary remodeling. Bone aging was characterized by: 1) secondary remodeling subendosteally; 2) increment of sealed primary vascular canals number; 3) increased calcium content of the cortex; 4) cortical and trabecular bone mass loss in specific ROIs. Taken together, the present data may give a morphological and morphometric basis to perform comparative studies on experimental models of osteoporosis in the rabbit. J. Morphol. 276:733–747, 2015.

Ghrelin Increases Beta-Catenin Level through Protein Kinase A Activation and Regulates OPG Expression in Rat Primary Osteoblasts

Ghrelin, by binding growth hormone secretagogue receptor (GHS-R), promotes osteoblast proliferation but the signaling mechanism of GHS-R on these cells remains unclear. Since canonical Wnt/β-catenin pathway is critically associated with bone homeostasis, we investigated its involvement in mediating ghrelin effects in osteoblasts and in osteoblast-osteoclast cross talk. Ghrelin (10−10M) significantly increased β-catenin levels in rat osteoblasts (rOB). This stimulatory action on β-catenin involves a specific interaction with GHS-R1a, as it is prevented by the selective GHS-R1a antagonist, D-Lys3-GHRP-6 (10−7M). The effect of ghrelin on β-catenin involves the phosphorylation and inactivation of GSK-3β via protein kinase A (PKA). Inhibition of PKA activity reduces the facilitatory action of ghrelin on β-catenin stabilization. Ghrelin treatment of rOB significantly increases the expression of osteoprotegerin (OPG), which plays an important role in the regulation of osteoclastogenesis, and this effect is blocked by D-Lys3-GHRP-6. Furthermore, ghrelin reduced RANKL/OPG ratio thus contrasting osteoclastogenesis. Accordingly, conditioned media from rOB treated with ghrelin decreased the number of multinucleated TRAcP+ cells as compared with the conditioned media from untreated-control rOB. Our data suggest new roles for ghrelin in modulating bone homeostasis via a specific interaction with GHSR-1a in osteoblasts with subsequent enhancement of both β-catenin levels and OPG expression.

The canalicular system and the osteoblast domain in human secondary osteons.

The lacunar–canalicular system in human secondary osteons was examined by two complementary techniques: light microscopy analysis of undecalcified thick sections and the SEM cortex‐fractured surface technique. Unlike the earlier definitions of ‘osteoblastic domain’ presented as the matrix volume produced by osteoblasts in the process of osteon infilling, this study measured the domain by the length of osteoblast dendritic processes. The domain extension was defined along radial vectors advancing from the reversal line towards the central canal. According to their lengths, domains were divided into three classes: peripheral, intermediate and internal. The mean length of peripheral domains was significantly shorter than those of the intermediate and internal domains. This suggests that the infilling process is modulated by an initial preparatory phase characterised by osteoblast adhesion to the wall of the cutting cone, and a limited matrix synthesis, followed by a regular matrix volume apposition organised in concentric layers. In addition to the radial canaliculae arranged along converging vectors in planes perpendicular to the central canal, we distinguished a further class of canaliculae, the equatorial canaliculae originating from the major perimeter of the lacuna and spreading out radially in the plane of the same lacuna (therefore, perpendicularly to the radial canaliculae). The whole lacunar–canalicular network was structured as a closed system around the vascular axis of the central canal with very few canaliculae crossing the reversal line and connecting the neighbouring osteons. These anatomical observations contribute to our knowledge of lacunar–canalicular system development.