Evaluation of the Effects of Covid 19 Infection on Bone Remodeling and Bone Fragility

NCT ID: NCT05352295

Last Updated: 2022-04-28

Basic Information

• Recruitment Status: UNKNOWN
• Total Enrollment: 80 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2021-02-18
• Study Completion Date: 2022-12-31

Brief Summary

Although SARS-CoV-2 infection and subsequent COVID-19 disease is regarded as a disease that primarily affects the lungs, it can also damage many other organs. This organ damage may increase the risk of long-term health problems, but much remains to be elucidated as to how COVID-19 infection will affect those who have contracted the infection over time. Since SARS-CoV-2 infection mainly affects elderly people, one of the aspects to be evaluated in the near future is its interaction with bone metabolism, which progressively worsens with advancing age. So far, data on bone metabolism in SARS-COV-2 infection are very scarce. Furthermore, it is not clear whether the incidence of osteoporosis and the risk of fracture may increase in patients after recovery from the infection, due to the interaction of their risk factors (old age, smoking, long-term bed rest). term, hypovitaminosis D and steroid treatment) with the COVID-19 inflammatory process. In patients after recovery from severe acute respiratory syndrome (SARS), osteonecrosis and bone abnormalities with reduced bone density were observed, which were partly but not entirely explained by short-term use of steroids. Infections, trauma and injuries induce the production of endogenous signaling mediators of the inflammatory response. Significantly higher serum concentrations of pro and anti-inflammatory cytokines, including IL-6, TNF-α, and IL-10, characterized by severe versus moderate cases, suggest that disease severity may be associated with a "cytokine storm. "[14]. The interaction between inflammatory molecules, such as cytokines, and the bone system is defined as "osteoimmunology" and osteoimmunological mediators, such as RANKL, OPG, RAGE, play a fundamental role in osteoclastogenesis in physiological and pathological conditions. Although the long-term effects of COVID-19 are still unknown, the alleged consequences of the disease would likely be similar to those of coronavirus-related diseases, including SARS (Severe acute respiratory syndrome). In the case of SARS, viral infection-mediated effects have been described that stimulate osteoclatogenesis. Similarly, the current SARS-Cov-2 could have a dual effect, both direct and indirect, on osteoclastogenesis and, consequently, on bone resorption: indirectly by inducing the cytokine storm that promotes bone resorption, direct by stimulating differentiation and osteoclastic activation through the activation of osteoimmunological mediators.

Detailed Description

The biological markers under study ( RANKL, OPG, RAGE) will be determined:

• The determinations will be performed on blood samples performed as part of the checks conducted in the normal diagnostic flow and using the residual material not used for routine diagnostics.

Clinical investigations of bone fragility:

• Radiographic investigations performed routinely (pre-operative and immediate post-operative)
• Laboratory tests required by clinical routine:

• Pre-operative: blood count, coagulation
• First post-operative sampling (1 post-operative day): complete blood count, coagulation
• Second post-operative sampling, if performed (3 postoperative day +/- 1 day): blood count and coagulation or each evaluated parameter, the following will be calculated:
• descriptive statistics (mean, standard deviation for variables with normal distribution, median and range for variables not normally distributed)
• differences between the two populations (Covid19 positive and Covid19 negative) by means of parametric or non-parametric tests based on the normality of the distribution of values
• sensitivity, specificity positive and negative predictive values, likelihood ratio for each test and for a combination of them Statistical analyzes will be performed using the GraphPad Prism V.5.03 computer package for Windows (GraphPad Software, San Diego, CA, www.graphpad.com).

Conditions

Bone Remodeling Bone Fragility Resulting From Covid19

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: OTHER

Study Groups

infected

40 patients admitted to the IRCCS Galeazzi Orthopedic Institute for fracture with Covid 19 infection ascertained by nasal pharyngeal swab during the patients' clinical routine

No interventions assigned to this group

not infected ( control)

40 patients admitted to the IRCCS Galeazzi Orthopedic Institute for fracture without Covid 19 infection ascertained by nasal pharyngeal swab during the patients' clinical routine

No interventions assigned to this group

Eligibility Criteria

Inclusion Criteria

age greater than or equal to 50 years

• patients in the emergency room for fracture of the proximal femur
• subjects of both sexes
• pathologies related to bone fragility (osteoporosis, fractures, parathyroid pathologies).
• signature of the informed consent
• having performed the nasopharyngeal swab for clinical practice to check for SARS Cov2 infection

Exclusion Criteria

• previous conditions of hypovitaminosis D
• steroid therapy
• Presence of autoimmune diseases or that can create alterations in the inflammatory response

• Minimum Eligible Age: 50 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Giuseppe Peretti, MD PhD

Role: PRINCIPAL_INVESTIGATOR

I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio

Locations

Istituto Ortopedico Galeazzi

Milan, , Italy

Site Status: RECRUITING

Countries

Italy

Central Contacts

Elena Cittera

Role: CONTACT

elena.cittera@grupposandonato.it

+39 0266214048

Sara Zacchetti

Role: CONTACT

sara.zacchetti@grupposandonato.it

Facility Contacts

Giuseppe Peretti, MdPhD

Role: primary

giuseppe.peretti@unimi.it

Other Identifiers

CovidBone

Identifier Type: -

Identifier Source: org_study_id