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      Immunogenicity of the BNT162b2 vaccine in frail or disabled nursing home residents: COVID‐A study

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          Abstract

          Background/Objectives

          The safety and immunogenicity of the BNT162b2 coronavirus disease 2019 (COVID‐19) vaccine in older adults with different frailty and disability profiles have not been well determined. Our objective was to analyze immunogenicity of the BNT162b2 mRNA COVID‐19 vaccine in older adults across frailty and disability profiles.

          Design

          Multicenter longitudinal cohort study.

          Setting and participants

          A total of 134 residents aged ≥65 years with different frailty and disability profiles in five long‐term care facilities (LTCFs) in Albacete, Spain.

          Intervention and measurements

          Residents were administered two vaccine doses as per the label, and antibody levels were determined 21.9 days (SD 9.3) after both the first and second dose. Functional variables were assessed using activities of daily living (Barthel Index), and frailty status was determined with the FRAIL instrument. Cognitive status and comorbidity were also evaluated.

          Results

          Mean age was 82.9 years (range 65–99), and 71.6% were female. The mean antibody titers in residents with and without previous COVID‐19 infection were 49,878 AU/ml and 15,274 AU/ml, respectively (mean difference 34,604; 95% confidence interval [CI]: 27,699–41,509). No severe adverse reactions were observed, after either vaccine dose. Those with prevaccination COVID‐19 had an increased antibody level after the vaccine ( B = 31,337; 95% CI: 22,725–39,950; p < 0.001). Frailty, disability, older age, sex, cognitive impairment, or comorbidities were not associated with different antibody titers.

          Conclusions

          The BNT162b2 mRNA COVID‐19 vaccine in older adults is safe and produces immunogenicity, independently of the frailty and disability profiles. Older adults in LTCFs should receive a COVID‐19 vaccine.

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          Most cited references26

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          Validation of a combined comorbidity index

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            The Global Deterioration Scale for assessment of primary degenerative dementia

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              A simple frailty questionnaire (FRAIL) predicts outcomes in middle aged African Americans.

              To validate the FRAIL scale. Longitudinal study. Community. Representative sample of African Americans age 49 to 65 years at onset of study. The 5-item FRAIL scale (fatigue, resistance, ambulation, illnesses, and loss of weight), at baseline and activities of daily living (ADLs), instrumental activities of daily living (IADLs), mortality, short physical performance battery (SPPB), gait speed, one-leg stand, grip strength and injurious falls at baseline and 9 years. Blood tests for CRP, SIL6R, STNFR1, STNFR2 and 25 (OH) vitamin D at baseline. Cross-sectionally the FRAIL scale correlated significantly with IADL difficulties, SPPB, grip strength and one-leg stand among participants with no baseline ADL difficulties (N=703) and those outcomes plus gait speed in those with no baseline ADL dependencies (N=883). TNFR1 was increased in pre-frail and frail subjects and CRP in some subgroups. Longitudinally (N=423 with no baseline ADL difficulties or N=528 with no baseline ADL dependencies), and adjusted for the baseline value for each outcome, being pre-frail at baseline significantly predicted future ADL difficulties, worse one-leg stand scores, and mortality in both groups, plus IADL difficulties in the dependence-excluded group. Being frail at baseline significantly predicted future ADL difficulties, IADL difficulties, and mortality in both groups, plus worse SPPB in the dependence-excluded group. This study has validated the FRAIL scale in a late middle-aged African American population. This simple 5-question scale is an excellent screening test for clinicians to identify frail persons at risk of developing disability as well as decline in health functioning and mortality.
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                Author and article information

                Contributors
                pabizanda@sescam.jccm.es
                Journal
                J Am Geriatr Soc
                J Am Geriatr Soc
                10.1111/(ISSN)1532-5415
                JGS
                Journal of the American Geriatrics Society
                John Wiley & Sons, Inc. (Hoboken, USA )
                0002-8614
                1532-5415
                02 April 2021
                June 2021
                : 69
                : 6 ( doiID: 10.1111/jgs.v69.6 )
                : 1441-1447
                Affiliations
                [ 1 ] Residencia de Mayores San Vicente de Paúl Diputación de Albacete Albacete Spain
                [ 2 ] Department of Geriatrics Complejo Hospitalario Universitario de Albacete Albacete Spain
                [ 3 ] CIBERFES Ministerio de Economía y Competitividad Spain
                [ 4 ] Facultad de Medicina Universidad de Castilla‐La Mancha Albacete Spain
                [ 5 ] Department of Rheumatology Complejo Hospitalario Universitario de Albacete Albacete Spain
                [ 6 ] Department of Microbiology Complejo Hospitalario Universitario de Albacete Albacete Spain
                [ 7 ] Diputación de Albacete Vasco Núñez de Balboa Facility Albacete Spain
                [ 8 ] Department of Statistics Foundation of the National Paraplegics Hospital of Toledo Toledo Spain
                [ 9 ] Long‐Term Care Facilities Coordination Complejo Hospitalario Universitario de Albacete Albacete Spain
                [ 10 ] Department of Physiology and Pharmacology Karolinska Institutet Stockholm Sweden
                [ 11 ] Department of Surgery and Cancer Imperial College, Hammersmith Hospital, ICTEM building London United Kingdom
                Author notes
                [*] [* ] Correspondence

                Pedro Abizanda, MD, PhD, Hospital Perpetuo Socorro, Complejo Hospitalario Universitario de Albacete, C/ Seminario 4, Albacete 02006, Spain.

                Email: pabizanda@ 123456sescam.jccm.es

                Author information
                https://orcid.org/0000-0002-4707-2963
                Article
                JGS17153
                10.1111/jgs.17153
                8250586
                33768521
                850d9a17-14a0-4961-a854-f0aa4309c69a
                © 2021 The American Geriatrics Society.

                This article is being made freely available through PubMed Central as part of the COVID-19 public health emergency response. It can be used for unrestricted research re-use and analysis in any form or by any means with acknowledgement of the original source, for the duration of the public health emergency.

                History
                : 12 March 2021
                : 10 March 2021
                : 12 March 2021
                Page count
                Figures: 1, Tables: 1, Pages: 7, Words: 3865
                Funding
                Funded by: Centro de Investigación Biomédica en Red Fragilidad y Envejecimiento Saludable , open-funder-registry 10.13039/100012619;
                Award ID: CB16/10/00408
                Funded by: Instituto de Salud Carlos III , open-funder-registry 10.13039/501100004587;
                Award ID: COV20/00004
                Categories
                Brief Report
                COVID‐19‐Related Content
                Brief Report
                Custom metadata
                2.0
                June 2021
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.0.4 mode:remove_FC converted:02.07.2021

                Geriatric medicine
                bnt162b2 vaccine,covid‐19,disability,frailty,immunogenicity,older adults
                Geriatric medicine
                bnt162b2 vaccine, covid‐19, disability, frailty, immunogenicity, older adults

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