Hepatitis E seroprevalence in recipients of renal transplants or haemodialysis in southwest England: A case-control study
Locally acquired HEV infection is increasingly recognized in developed countries. Anti‐HEV IgG seroprevalence has been shown to be high in haemodialysis patients in a number of previous studies, employing assays of uncertain sensitivity. The aim of this study was to investigate anti‐HEV IgG seroprev...
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Published in | Journal of medical virology Vol. 85; no. 2; pp. 266 - 271 |
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Abstract | Locally acquired HEV infection is increasingly recognized in developed countries. Anti‐HEV IgG seroprevalence has been shown to be high in haemodialysis patients in a number of previous studies, employing assays of uncertain sensitivity. The aim of this study was to investigate anti‐HEV IgG seroprevalence in recipients of haemodialysis and renal transplants compared to a control group using a validated, highly sensitive assay. Eighty‐eight patients with functioning renal transplants and 76 receiving chronic haemodialysis were tested for HEV RNA and anti‐HEV IgG and IgM. Six hundred seventy controls were tested for anti‐HEV IgG. Anti‐HEV IgG was positive in 28/76 (36.8%) of haemodialysis and 16/88 (18.2%) of transplant patients. HEV RNA was not found in any patient. 126/670 (18.8%) of control subjects were anti‐HEV IgG positive. After adjusting for age and sex, there was a significantly higher anti‐HEV IgG seroprevalence amongst haemodialysis patients compared to controls (OR = 1.97, 95% CI = 1.16–3.31, P = 0.01) or transplant recipients (OR = 2.63, 95% CI = 1.18–6.07, P = 0.02). Patients with a functioning transplant showed no difference in anti‐HEV IgG seroprevalence compared to controls. The duration of haemodialysis or receipt of blood products were not significant risk factors for HEV IgG positivity. Patients receiving haemodialysis have a higher seroprevalence of anti‐HEV IgG than both age‐ and sex‐matched controls and a cohort of renal transplant patients. None of the haemodialysis patients had evidence of chronic infection. The reason haemodialysis patients have a high seroprevalence remains uncertain and merits further study. J. Med. Virol. 85:266–271, 2013. © 2012 Wiley Periodicals, Inc. |
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AbstractList | Locally acquired HEV infection is increasingly recognized in developed countries. Anti-HEV IgG seroprevalence has been shown to be high in haemodialysis patients in a number of previous studies, employing assays of uncertain sensitivity. The aim of this study was to investigate anti-HEV IgG seroprevalence in recipients of haemodialysis and renal transplants compared to a control group using a validated, highly sensitive assay. Eighty-eight patients with functioning renal transplants and 76 receiving chronic haemodialysis were tested for HEV RNA and anti-HEV IgG and IgM. Six hundred seventy controls were tested for anti-HEV IgG. Anti-HEV IgG was positive in 28/76 (36.8%) of haemodialysis and 16/88 (18.2%) of transplant patients. HEV RNA was not found in any patient. 126/670 (18.8%) of control subjects were anti-HEV IgG positive. After adjusting for age and sex, there was a significantly higher anti-HEV IgG seroprevalence amongst haemodialysis patients compared to controls (OR=1.97, 95% CI=1.16-3.31, P=0.01) or transplant recipients (OR=2.63, 95% CI=1.18-6.07, P=0.02). Patients with a functioning transplant showed no difference in anti-HEV IgG seroprevalence compared to controls. The duration of haemodialysis or receipt of blood products were not significant risk factors for HEV IgG positivity. Patients receiving haemodialysis have a higher seroprevalence of anti-HEV IgG than both age- and sex-matched controls and a cohort of renal transplant patients. None of the haemodialysis patients had evidence of chronic infection. The reason haemodialysis patients have a high seroprevalence remains uncertain and merits further study. J. Med. Virol. 85:266-271, 2013. [copy 2012 Wiley Periodicals, Inc. Locally acquired HEV infection is increasingly recognized in developed countries. Anti-HEV IgG seroprevalence has been shown to be high in haemodialysis patients in a number of previous studies, employing assays of uncertain sensitivity. The aim of this study was to investigate anti-HEV IgG seroprevalence in recipients of haemodialysis and renal transplants compared to a control group using a validated, highly sensitive assay. Eighty-eight patients with functioning renal transplants and 76 receiving chronic haemodialysis were tested for HEV RNA and anti-HEV IgG and IgM. Six hundred seventy controls were tested for anti-HEV IgG. Anti-HEV IgG was positive in 28/76 (36.8%) of haemodialysis and 16/88 (18.2%) of transplant patients. HEV RNA was not found in any patient. 126/670 (18.8%) of control subjects were anti-HEV IgG positive. After adjusting for age and sex, there was a significantly higher anti-HEV IgG seroprevalence amongst haemodialysis patients compared to controls (OR=1.97, 95% CI=1.16-3.31, P=0.01) or transplant recipients (OR=2.63, 95% CI=1.18-6.07, P=0.02). Patients with a functioning transplant showed no difference in anti-HEV IgG seroprevalence compared to controls. The duration of haemodialysis or receipt of blood products were not significant risk factors for HEV IgG positivity. Patients receiving haemodialysis have a higher seroprevalence of anti-HEV IgG than both age- and sex-matched controls and a cohort of renal transplant patients. None of the haemodialysis patients had evidence of chronic infection. The reason haemodialysis patients have a high seroprevalence remains uncertain and merits further study. J. Med. Virol. 85:266-271, 2013. © 2012 Wiley Periodicals, Inc. [PUBLICATION ABSTRACT] Locally acquired HEV infection is increasingly recognized in developed countries. Anti‐HEV IgG seroprevalence has been shown to be high in haemodialysis patients in a number of previous studies, employing assays of uncertain sensitivity. The aim of this study was to investigate anti‐HEV IgG seroprevalence in recipients of haemodialysis and renal transplants compared to a control group using a validated, highly sensitive assay. Eighty‐eight patients with functioning renal transplants and 76 receiving chronic haemodialysis were tested for HEV RNA and anti‐HEV IgG and IgM. Six hundred seventy controls were tested for anti‐HEV IgG. Anti‐HEV IgG was positive in 28/76 (36.8%) of haemodialysis and 16/88 (18.2%) of transplant patients. HEV RNA was not found in any patient. 126/670 (18.8%) of control subjects were anti‐HEV IgG positive. After adjusting for age and sex, there was a significantly higher anti‐HEV IgG seroprevalence amongst haemodialysis patients compared to controls (OR = 1.97, 95% CI = 1.16–3.31, P = 0.01) or transplant recipients (OR = 2.63, 95% CI = 1.18–6.07, P = 0.02). Patients with a functioning transplant showed no difference in anti‐HEV IgG seroprevalence compared to controls. The duration of haemodialysis or receipt of blood products were not significant risk factors for HEV IgG positivity. Patients receiving haemodialysis have a higher seroprevalence of anti‐HEV IgG than both age‐ and sex‐matched controls and a cohort of renal transplant patients. None of the haemodialysis patients had evidence of chronic infection. The reason haemodialysis patients have a high seroprevalence remains uncertain and merits further study. J. Med. Virol. 85:266–271, 2013. © 2012 Wiley Periodicals, Inc. Locally acquired HEV infection is increasingly recognized in developed countries. Anti-HEV IgG seroprevalence has been shown to be high in haemodialysis patients in a number of previous studies, employing assays of uncertain sensitivity. The aim of this study was to investigate anti-HEV IgG seroprevalence in recipients of haemodialysis and renal transplants compared to a control group using a validated, highly sensitive assay. Eighty-eight patients with functioning renal transplants and 76 receiving chronic haemodialysis were tested for HEV RNA and anti-HEV IgG and IgM. Six hundred seventy controls were tested for anti-HEV IgG. Anti-HEV IgG was positive in 28/76 (36.8%) of haemodialysis and 16/88 (18.2%) of transplant patients. HEV RNA was not found in any patient. 126/670 (18.8%) of control subjects were anti-HEV IgG positive. After adjusting for age and sex, there was a significantly higher anti-HEV IgG seroprevalence amongst haemodialysis patients compared to controls (OR = 1.97, 95% CI = 1.16-3.31, P = 0.01) or transplant recipients (OR = 2.63, 95% CI = 1.18-6.07, P = 0.02). Patients with a functioning transplant showed no difference in anti-HEV IgG seroprevalence compared to controls. The duration of haemodialysis or receipt of blood products were not significant risk factors for HEV IgG positivity. Patients receiving haemodialysis have a higher seroprevalence of anti-HEV IgG than both age- and sex-matched controls and a cohort of renal transplant patients. None of the haemodialysis patients had evidence of chronic infection. The reason haemodialysis patients have a high seroprevalence remains uncertain and merits further study. Locally acquired HEV infection is increasingly recognized in developed countries. Anti‐HEV IgG seroprevalence has been shown to be high in haemodialysis patients in a number of previous studies, employing assays of uncertain sensitivity. The aim of this study was to investigate anti‐HEV IgG seroprevalence in recipients of haemodialysis and renal transplants compared to a control group using a validated, highly sensitive assay. Eighty‐eight patients with functioning renal transplants and 76 receiving chronic haemodialysis were tested for HEV RNA and anti‐HEV IgG and IgM. Six hundred seventy controls were tested for anti‐HEV IgG. Anti‐HEV IgG was positive in 28/76 (36.8%) of haemodialysis and 16/88 (18.2%) of transplant patients. HEV RNA was not found in any patient. 126/670 (18.8%) of control subjects were anti‐HEV IgG positive. After adjusting for age and sex, there was a significantly higher anti‐HEV IgG seroprevalence amongst haemodialysis patients compared to controls (OR = 1.97, 95% CI = 1.16–3.31, P = 0.01) or transplant recipients (OR = 2.63, 95% CI = 1.18–6.07, P = 0.02). Patients with a functioning transplant showed no difference in anti‐HEV IgG seroprevalence compared to controls. The duration of haemodialysis or receipt of blood products were not significant risk factors for HEV IgG positivity. Patients receiving haemodialysis have a higher seroprevalence of anti‐HEV IgG than both age‐ and sex‐matched controls and a cohort of renal transplant patients. None of the haemodialysis patients had evidence of chronic infection. The reason haemodialysis patients have a high seroprevalence remains uncertain and merits further study. J. Med. Virol. 85:266–271, 2013. © 2012 Wiley Periodicals, Inc. |
Author | Hunter, Jeremy G. Harrison, Alex Lin, Nan X. Parry, Rob Johnston, Paul Scobie, Linda Crossan, Claire Stratton, Jon Dalton, Harry R. Dickinson, Steve Madden, Richie Ellis, Vic Henley, William E. Prescott, Oliver R. Bendall, Richard P. |
Author_xml | – sequence: 1 givenname: Alex surname: Harrison fullname: Harrison, Alex organization: Department of Nephrology, Royal Cornwall Hospital Truro, Cornwall, United Kingdom – sequence: 2 givenname: Linda surname: Scobie fullname: Scobie, Linda organization: Glasgow Caledonian University, Glasgow, Scotland, United Kingdom – sequence: 3 givenname: Claire surname: Crossan fullname: Crossan, Claire organization: Glasgow Caledonian University, Glasgow, Scotland, United Kingdom – sequence: 4 givenname: Rob surname: Parry fullname: Parry, Rob organization: Department of Nephrology, Royal Cornwall Hospital Truro, Cornwall, United Kingdom – sequence: 5 givenname: Paul surname: Johnston fullname: Johnston, Paul organization: Department of Nephrology, Royal Cornwall Hospital Truro, Cornwall, United Kingdom – sequence: 6 givenname: Jon surname: Stratton fullname: Stratton, Jon organization: Department of Nephrology, Royal Cornwall Hospital Truro, Cornwall, United Kingdom – sequence: 7 givenname: Steve surname: Dickinson fullname: Dickinson, Steve organization: Department of Nephrology, Royal Cornwall Hospital Truro, Cornwall, United Kingdom – sequence: 8 givenname: Vic surname: Ellis fullname: Ellis, Vic organization: Clinical Microbiology, Royal Cornwall Hospital Truro, Cornwall, United Kingdom – sequence: 9 givenname: Jeremy G. surname: Hunter fullname: Hunter, Jeremy G. organization: Cornwall Gastrointestinal Unit, Royal Cornwall Hospital Truro, Cornwall, United Kingdom – sequence: 10 givenname: Oliver R. surname: Prescott fullname: Prescott, Oliver R. organization: Cornwall Gastrointestinal Unit, Royal Cornwall Hospital Truro, Cornwall, United Kingdom – sequence: 11 givenname: Richie surname: Madden fullname: Madden, Richie organization: Cornwall Gastrointestinal Unit, Royal Cornwall Hospital Truro, Cornwall, United Kingdom – sequence: 12 givenname: Nan X. surname: Lin fullname: Lin, Nan X. organization: Institute of Health Service Research, University of Exeter Medical School, Exeter, United Kingdom – sequence: 13 givenname: William E. surname: Henley fullname: Henley, William E. organization: Institute of Health Service Research, University of Exeter Medical School, Exeter, United Kingdom – sequence: 14 givenname: Richard P. surname: Bendall fullname: Bendall, Richard P. organization: Clinical Microbiology, Royal Cornwall Hospital Truro, Cornwall, United Kingdom – sequence: 15 givenname: Harry R. surname: Dalton fullname: Dalton, Harry R. email: harry.dalton@rcht.cornwall.nhs.uk organization: Cornwall Gastrointestinal Unit, Royal Cornwall Hospital Truro, Cornwall, United Kingdom |
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Keywords | Kidney disease Urinary system disease Prevalence hepatitis E virus (HEV) chronic renal failure Hepatic disease Recipient Serology Case control study Epidemiology Hepatitis E virus Infection Virus Calicivirus Chronic Caliciviridae Viral disease Renal failure Digestive diseases Viral hepatitis E |
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Title | Hepatitis E seroprevalence in recipients of renal transplants or haemodialysis in southwest England: A case-control study |
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