4.5 Article

Tacrolimus trough-level variability predicts long-term allograft survival following kidney transplantation

Journal

JOURNAL OF NEPHROLOGY
Volume 29, Issue 2, Pages 269-276

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s40620-015-0230-0

Keywords

Transplantation; Tacrolimus; Variability; Kidney

Ask authors/readers for more resources

The purpose of this study is to investigate tacrolimus trough-level variability from 3 to 12 months following transplantation and its association with allograft survival in renal transplant recipients. In this observational cohort study, tacrolimus trough-level variability was used as the predictor of all-cause allograft failure (defined as return to dialysis) and patient survival (all-cause mortality). In total, 394 transplants were included in the analysis. Sixty-two transplants failed during the study. Tacrolimus trough-level variability across quartile groups were: Q1 median variability 12.5 %, range 4.76-15.71 % (n = 99), Q2 median variability 18.17 %, range 15.74-21.29 % (n = 96), Q3 median variability 24.63 % range 21.42-28.88 % (n = 100), Q4 median variability 36.91 %, range 28.91-81.9 % (n = 99). Higher tacrolimus trough-level variability was associated with inferior allograft survival in univariate models [hazard ratio per quartile increase (HR), 1.46, 95 % CI 1.16-1.83, p value = 0.001] and multivariate models (HR 1.36, 95 % CI 1.05-1.78, p value = 0.019). Higher tacrolimus trough-level variability was not associated with patient survival; univariate model (HR 1.25, 95 % CI 0.90-1.74, p value = 0.17), multivariate model (HR 1.25, 95 % CI 0.86-1.83, p value = 0.23). Inferior renal allograft survival was observed in recipients with higher variability in tacrolimus trough-levels.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

Article Urology & Nephrology

Utility of Genomic Testing after Renal Biopsy

Susan L. Murray, Anthony Dorman, Katherine A. Benson, Dervla M. Connaughton, Caragh P. Stapleton, Neil K. Fennelly, Claire Kennedy, Ciara A. McDonnell, Kendrah Kidd, Sarah M. Cormican, Louise A. Ryan, Peter Lavin, Mark A. Little, Anthony J. Bleyer, Brendan Doyle, Gianpiero L. Cavalleri, Friedhelm Hildebrandt, Peter J. Conlon

AMERICAN JOURNAL OF NEPHROLOGY (2020)

Article Surgery

Renal transplant outcomes in patients with autosomal dominant tubulointerstitial kidney disease

Sarah Cormican, Claire Kennedy, Dervla M. Connaughton, Patrick O'Kelly, Susan Murray, Martina Zivna, Stanislav Kmoch, Neil K. Fennelly, Katherine A. Benson, Eoin T. Conlon, Gianpiero L. Cavalleri, Claire Foley, Brendan Doyle, Anthony Dorman, Mark A. Little, Peter Lavin, Kendrah Kidd, Anthony J. Bleyer, Peter J. Conlon

CLINICAL TRANSPLANTATION (2020)

Article Genetics & Heredity

Phenotype expansion of heterozygous FOXC1 pathogenic variants toward involvement of congenital anomalies of the kidneys and urinary tract (CAKUT)

Chen-Han Wilfred Wu, Nina Mann, Makiko Nakayama, Dervla M. Connaughton, Rufeng Dai, Caroline M. Kolvenbach, Franziska Kause, Isabel Ottlewski, Chunyan Wang, Verena Klambt, Steve Seltzsam, Ethan W. Lai, Aravind Selvin, Prabha Senguttuva, Olaf Bodamer, Deborah R. Stein, Sherif El Desoky, Jameela A. Kari, Velibor Tasic, Stuart B. Bauer, Shirlee Shril, Friedhelm Hildebrandt

GENETICS IN MEDICINE (2020)

Article Genetics & Heredity

Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations

Dervla M. Connaughton, Rufeng Dai, Danielle J. Owen, Jonathan Marquez, Nina Mann, Adda L. Graham-Paquin, Makiko Nakayama, Etienne Coyaud, Estelle Mn Laurent, Jonathan R. St-Germain, Lot Snijders Blok, Arianna Vino, Verena Klambt, Konstantin Deutsch, Chen-Han Wilfred Wu, Caroline M. Kolvenbach, Franziska Kause, Isabel Ottlewski, Ronen Schneider, Thomas M. Kitzler, Amar J. Majmundar, Florian Buerger, Ana C. Onuchic-Whitford, Mao Youying, Amy Kolb, Daanya Salmanullah, Evan Chen, Amelie T. van der Ven, Jia Rao, Hadas Ityel, Steve Seltzsam, Johanna M. Rieke, Jing Chen, Asaf Vivante, Daw-Yang Hwang, Stefan Kohl, Gabriel C. Dworschak, Tobias Hermle, Marielle Alders, Tobias Bartolomaeus, Stuart B. Bauer, Michelle A. Baum, Eva H. Brilstra, Thomas D. Challman, Jacob Zyskind, Carrie E. Costin, Katrina M. Dipple, Floor A. Duijkers, Marcia Ferguson, David R. Fitzpatrick, Roger Fick, Ian A. Glass, Peter J. Hulick, Antonie D. Kline, Ilona Krey, Selvin Kumar, Weining Lu, Elysa J. Marco, Ingrid M. Wentzensen, Heather C. Mefford, Konrad Platzer, Inna S. Povolotskaya, Juliann M. Savatt, Natalia Shcherbakova, Prabha Senguttuvan, Audrey E. Squire, Deborah R. Stein, Isabelle Thiffault, Victoria Y. Voinova, Michael J. G. Somers, Michael A. Ferguson, Avram Z. Traum, Ghaleb H. Daouk, Ankana Daga, Nancy M. Rodig, Paulien A. Terhal, Ellen van Binsbergen, Loai A. Eid, Velibor Tasic, Hila Milo Rasouly, Tze Y. Lim, Dina F. Ahram, Ali G. Gharavi, Heiko M. Reutter, Heidi L. Rehm, Daniel G. MacArthur, Monkol Lek, Kristen M. Laricchia, Richard P. Lifton, Hong Xu, Shrikant M. Mane, Simone Sanna-Cherchi, Andrew D. Sharrocks, Brian Raught, Simon E. Fisher, Maxime Bouchard, Mustafa K. Khokha, Shirlee Shril, Friedhelm Hildebrandt

AMERICAN JOURNAL OF HUMAN GENETICS (2020)

Article Genetics & Heredity

DAAM2 Variants Cause Nephrotic Syndrome via Actin Dysregulation

Ronen Schneider, Konstantin Deutsch, Gregory J. Hoeprich, Jonathan Marquez, Tobias Hermle, Daniela A. Braun, Steve Seltzsam, Thomas M. Kitzler, Youying Mao, Florian Buerger, Amar J. Majmundar, Ana C. Onuchic-Whitford, Caroline M. Kolvenbach, Luca Schierbaum, Sophia Schneider, Abdul A. Halawi, Makiko Nakayama, Nina Mann, Dervla M. Connaughton, Verena Klambt, Matias Wagner, Korbinian M. Riedhammer, Lutz Renders, Yoshichika Katsura, Dean Thumkeo, Neveen A. Soliman, Shrikant Mane, Richard P. Lifton, Shirlee Shril, Mustafa K. Khokha, Julia Hoefele, Bruce L. Goode, Friedhelm Hildebrandt

AMERICAN JOURNAL OF HUMAN GENETICS (2020)

Article Biochemistry & Molecular Biology

The genetic landscape of polycystic kidney disease in Ireland

Katherine A. Benson, Susan L. Murray, Sarah R. Senum, Elhussein Elhassan, Eoin T. Conlon, Claire Kennedy, Shane Conlon, Edmund Gilbert, Dervla Connaughton, Paul O'Hara, Sarah Khamis, Sarah Cormican, Lawrence C. Brody, Anne M. Molloy, Sally Ann Lynch, Liam Casserly, Matthew D. Griffin, Robert Carton, Kevin Yachnin, Peter C. Harris, Gianpiero L. Cavalleri, Peter Conlon

Summary: PKDs are the most common Mendelian forms of renal disease characterized by fluid-filled renal cysts, leading to progressive kidney function loss. Ireland is a valuable area for genetic studies of PKD, with diagnostic rates of 71-83% in Irish patients using different variant classification guidelines. The study reveals a spectrum of Irish autosomal dominant PKD pathogenic variants and highlights issues with implementing ACMG guidelines for variant pathogenicity interpretation in clinical genetics.

EUROPEAN JOURNAL OF HUMAN GENETICS (2021)

Article Genetics & Heredity

Potential Pitfalls in Pre-implantation Genetic Diagnosis in a Patient with Tuberous Sclerosis and Isolated Mosaicism for a TSC2 Variant in Renal Tissue

Kristin M. Ikeda, Andrew A. House, Deryla M. Connaughton, Stephen E. Pautler, Victoria Mok Siu, Michelle-Lee Jones

Summary: Tuberous sclerosis complex (TSC) is an autosomal dominant disorder primarily caused by mutations in the TSC1 or TSC2 genes, with cases of mosaicism sometimes identified. The study reported a TSC case where a likely pathogenic variant was detected in renal tissue by not in other tissues. This highlights the challenges in counseling patients with mosaicism about reproductive risks and prenatal diagnostics.

MOLECULAR SYNDROMOLOGY (2021)

Article Genetics & Heredity

Exome survey of individuals affected by VATER/VACTERL with renal phenotypes identifies phenocopies and novel candidate genes

Caroline M. Kolvenbach, Amelie T. van der Ven, Franziska Kause, Shirlee Shril, Marcello Scala, Dervla M. Connaughton, Nina Mann, Makiko Nakayama, Rufeng Dai, Thomas M. Kitzler, Ronen Schneider, Luca Schierbaum, Sophia Schneider, Andrea Accogli, Annalaura Torella, Gianluca Piatelli, Vincenzo Nigro, Valeria Capra, Bernd Hoppe, Stefanie Maerzheuser, Eberhard Schmiedeke, Heidi L. Rehm, Shrikant Mane, Richard P. Lifton, Gabriel C. Dworschak, Alina C. Hilger, Heiko Reutter, Friedhelm Hildebrandt

Summary: VATER/VACTERL is a rare genetic disease characterized by a combination of vertebral defects, anorectal malformations, cardiac anomalies, tracheoesophageal fistula, renal malformations, and limb anomalies. Exome sequencing identified potentially pathogenic variants in six individuals with a renal VATER/VACTERL phenotype, implicating novel genetic causes. This study reveals six genes associated with renal malformations in VATER/VACTERL individuals.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2021)

Article Genetics & Heredity

A truncating NRIP1 variant in an Arabic family with congenital anomalies of the kidneys and urinary tract

Bixia Zheng, Chunyan Wang, Steve Seltzsam, Sophia Schneider, Luca Schierbaum, Wilfred Wu, Rufeng Dai, Dervla M. Connaughton, Makiko Nakayama, Nina Mann, Stuart B. Bauer, Hazem S. Awad, Loai A. Eid, Velibor Tasic, Shirlee Shril, Friedhelm Hildebrandt

Summary: Congenital anomalies of the kidneys and urinary tract (CAKUT) can be caused by mutations in NRIP1, as confirmed by the discovery of a second family with NRIP1 variant.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2022)

Article Transplantation

Whole-exome sequencing identifies FOXL2, FOXA2 and FOXA3 as candidate genes for monogenic congenital anomalies of the kidneys and urinary tract

Bixia Zheng, Steve Seltzsam, Chunyan Wang, Luca Schierbaum, Sophia Schneider, Chen-Han Wilfred Wu, Rufeng Dai, Dervla M. Connaughton, Makiko Nakayama, Nina Mann, Natasa Stajic, Shrikant Mane, Stuart B. Bauer, Velibor Tasic, Hyun Joo Nam, Shirlee Shril, Friedhelm Hildebrandt

Summary: This study identified FOXL2, FOXA2, and FOXA3 as novel monogenic candidate genes associated with CAKUT, supporting the utility of a paralog-based approach to discover mutated genes associated with human disease.

NEPHROLOGY DIALYSIS TRANSPLANTATION (2022)

Article Genetics & Heredity

Whole exome sequencing identifies potential candidate genes for spina bifida derived from mouse models

Chunyan Wang, Steve Seltzsam, Bixia Zheng, Chen-Han Wilfred Wu, Camille Nicolas-Frank, Kirollos Yousef, Kit Sing Au, Nina Mann, Dalia Pantel, Sophia Schneider, Luca Schierbaum, Thomas M. Kitzler, Dervla M. Connaughton, Youying Mao, Rufeng Dai, Makiko Nakayama, Jameela A. Kari, Sherif El Desoky, Mohammed Shalaby, Loai A. Eid, Hazem S. Awad, Velibor Tasic, Shrikant M. Mane, Richard P. Lifton, Michelle A. Baum, Shirlee Shril, Carlos R. Estrada, Friedhelm Hildebrandt

Summary: Spina bifida is the second most common nonlethal congenital malformation. Whole exome sequencing can help identify potential candidate genes for spina bifida, which may be caused by monogenic genes. Through the study, 136 potential candidate genes were identified, and 6 likely deleterious variants were found in 50 spina bifida cases. Additionally, 12 genes were identified as potential new candidate genes through exome-wide analysis.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2022)

Article Genetics & Heredity

Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUT

Steve Seltzsam, Chunyan Wang, Bixia Zheng, Nina Mann, Dervla M. Connaughton, Chen-Han Wilfred Wu, Sophia Schneider, Luca Schierbaum, Franziska Kause, Caroline M. Kolvenbach, Makiko Nakayama, Rufeng Dai, Isabel Ottlewski, Ronen Schneider, Konstantin Deutsch, Florian Buerger, Verena Klaembt, Youying Mao, Ana C. Onuchic-Whitford, Camille Nicolas-Frank, Kirollos Yousef, Dalia Pantel, Ethan W. Lai, Daanya Salmanullah, Amar J. Majmundar, Stuart B. Bauer, Nancy M. Rodig, Michael J. G. Somers, Avram Z. Traum, Deborah R. Stein, Ankana Daga, Michelle A. Baum, Ghaleb H. Daouk, Velibor Tasic, Hazem S. Awad, Loai A. Eid, Sherif El Desoky, Mohammed Shalaby, Jameela A. Kari, Hanan M. Fathy, Neveen A. Soliman, Shrikant M. Mane, Shirlee Shril, Michael A. Ferguson, Friedhelm Hildebrandt

Summary: The study explores the use of reverse phenotyping to enhance molecular genetic diagnostics in CAKUT by re-examining cases for clinical symptoms that may have been overlooked during the initial diagnosis using exome sequencing.

GENETICS IN MEDICINE (2022)

Article Urology & Nephrology

The utility of a genetic kidney disease clinic employing a broad range of genomic testing platforms: experience of the Irish Kidney Gene Project

Elhussein A. E. Elhassan, Susan L. Murray, Dervla M. Connaughton, Claire Kennedy, Sarah Cormican, Cliona Cowhig, Caragh Stapleton, Mark A. Little, Kendrah Kidd, Anthony J. Bleyer, Martina Zivna, Stanislav Kmoch, Neil K. Fennelly, Brendan Doyle, Anthony Dorman, Matthew D. Griffin, Liam Casserly, Peter C. Harris, Friedhelm Hildebrandt, Gianpiero L. Cavalleri, Katherine A. Benson, Peter J. Conlon

Summary: This study describes the clinical utility and valuable impact of a specialized clinic for genetic kidney diseases, which uses various genomic sequencing strategies for genetic testing. The clinic achieved a high molecular diagnostic rate and helped confirm or reclassify the diagnoses of patients. The implementation of this clinic has resulted in direct clinical and therapeutic benefits for affected patients.

JOURNAL OF NEPHROLOGY (2022)

Meeting Abstract Medicine, General & Internal

The utility of an inherited kidney disease clinic employing a broad range of genomic testing platforms: Experience of the Irish Kidney Gene Project

Elhussein A. E. Elhassan, Susan L. Murray, Dervla Connaughton, Claire Kennedy, Kane Collins, Edmund Gilbert, Mark Little, Gianpiero Cavalleri, Peter Conlon

IRISH JOURNAL OF MEDICAL SCIENCE (2022)

Correction Neurosciences

Control of Motoneuron Survival by Angiogenin (vol 28, pg 14056, 2008)

Dairin Kieran, Jordi Sebastia, Matthew J. Greenway, Matthew A. King, Dervla Connaughton, Caoimhin G. Concannon, Beau Fenner, Orla Hardiman, Jochen H. M. Prehn

JOURNAL OF NEUROSCIENCE (2021)

No Data Available