Blog - INTERNET MÉDICA

Doença Glomerular Online (Glomerular Disease)

Por Paulo Leite 20/05/2019

■ Management and treatment of glomerular diseases (part 1): conclusions from a Kidney Disease: Improving global outcomes (KDIGO) Controversies Conference

J Floege, S J Barbour, D C Cattrans et al

Kidney International 2019, vol 95 (2): 268-280

https://www.kidney-international.org/article/S0085-2538(18)30809-3/fulltext

■ Management and treatment of glomerular diseases (part 2): conclusions from a Kidney Disease: Improving global outcomes (KDIGO) Controversies Conference

B H Rovin, D J Caster, D C Cattran et al

Kidney International 2019, vol 95 (2): 291-295

https://www.kidney-international.org/article/S0085-2538(18)30811-1/fulltext

■ Adiposity and risk of decline in glomerular filtration rate: meta-analysis of individual participant data in a global consortium

A R Chang, M E Grams, S H Ballew et al

BMJ 2019, vol 364: k5301

https://www.bmj.com/content/364/bmj.k5301

■ Abdominal obesity and reduction of glomerular filtration.

Dias, Raimunda Sheyla Carneiro et al.

Rev. Assoc. Med. Bras., Apr 2018, vol.64, no.4, p.346-353

http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0104-42302018000400346&lng=en&nrm=iso&tlng=en

■ Rituximab for anti-glomerular basement membrane disease

Rashmi Jain, Hanna Dgheim, Andrew S. Bomback

Kidney Int Rep. 2019 Apr; 4(4): 614–618

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6451084/

■ Dysproteinemias and glomerular disease

Nelson Leung, Maria E. Drosou, Samih H. Nasr

Clin J Am Soc Nephrol. 2018 Jan 6; 13(1): 128–139

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5753301/

■ Improving the prognosis of patients with severely decreased glomerular filtration rate (CKD G4+) : conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO)

K Eckardt, N Bansal, J Coresh et al

Kidney International 2018, vol 93 (6): p1281-1292

https://www.kidney-international.org/article/S0085-2538(18)30136-4/fulltext

■ Toward individual glomerular phenotyping: advent of precision medicine in kidney biopsies

K Sharma, L Pasa-Tolic

Kidney International 2018, vol 93 (6): p1265-81-1267

https://www.kidney-international.org/article/S0085-2538(18)30192-3/fulltext

■ The glomerular disease study and trial consortium: a grassroots initiative to foster collaboration and innovation

Ali Poyan Mehr, Maryam Sadeghi-Najafabadi, Kristi Chau et al

Kidney Int Rep. 2019 Jan; 4(1): 20–29

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6308822/

■ Glomerular disease in women

Kate Wiles, Liz Lightstone

Kidney Int Rep. 2018 Mar; 3(2): 258–270

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5932310/

■ Glucocorticoids in the treatment of glomerular diseases: pitfalls and pearls

Claudio Ponticelli, Francesco Locatelli

Clin J Am Soc Nephrol. 2018 May 7; 13(5): 815–82

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5969489/

■ Dr Paulo Fernando Leite

Cardiologia/Prevenção Cardiovascular

Estratificação de Risco Cardiovascular

Novo endereço:

Consultório: Rua Padre Rolim 815/sala 815

Tel: 33245518 (Consulta Particular/Unimed)

– Centro Médico Unimed BH/Contagem/Pedro I

Belo Horizonte/MG/Brasil

CRMMG: 7026

Email: pfleite1873@gmail.com

Doença Renal Policística Online (Polycystic Kidney Disease)

Por Paulo Leite 20/05/2019

¨A doença renal policística hereditária é uma desordem genética, podendo ser de caráter autossômica dominante (DRPAD) ou autossômica recessiva (DRPRD). Corresponde a uma insuficiência renal crônica de progressão lenta, caracterizada pelo desenvolvimento e crescimento progressivos de cistos renais, que começam a ser detectáveis quando já são tão numerosos e grandes, que ocupam o lugar do tecido renal normal, comprimindo-o e destruindo-o com o tempo, levando à falência renal terminal. A doença renal policística autossômica dominante (DRPAD) é a enfermidade renal hereditária mais comum em seres humanos. Reconhecida como doença monogênica multissistêmica, é caracterizada por progressivo crescimento e desenvolvimento de múltiplos cistos renais bilaterais que destroem o parênquima funcional, bem como por manifestações extrarrenais (cistos em outros órgãos, anormalidade valvular cardíaca, aneurismas cerebrais, hérnias abdominais, dores pelo corpo, colecistopatia calculosa e doença diverticular).¨

■ Urinary T cells correlate with rate of renal function in autosomal dominant polycystic kidney disease

Kurt A. Zimmerman, Nancy M. Gonzalez, Phillip Chumley, et al

Physiol Rep. 2019 Jan; 7(1): e13951

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6328912/

■ Management of autosomal-dominant polycystic kidney disease – state-of-the-art

Roman-Ulrich Müller, Thomas Benzing

Clin Kidney J. 2018 Dec; 11(Suppl 1): i2–i13

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6295602/

■ Updated Canadan Expert Consensus on assessing risk of disease progression and pharmacological management of autosomal dominant polycystic kidney disease

Steven Soroka, Ahsan Alam, Micheli Bevilacqua et al

Can J Kidney Health Dis. 2018; 5: 2054358118801589

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6187423/

■ Urinary biomarkers to identify autosomal dominant polycystic kidney disease patients with a high likelihood of disease progression

Lianne Messchendorp, Esther Meijer, Wendy E. Boertien

DIPAK Consortium

Kidney Int Rep. 2018 Mar; 3(2): 291–301

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5932128/

■ A case of congenital left ventricular diverticulum in a patient with autosomal dominant polycystic kidney disease: possible mechanistic link beteween polycystin and ventricular diverticulum

Seishi Aihara, Shunsuke Yamada, Hidenori Matsusaka, Rami Tashiro et al

CEN Case Rep. 2018 Nov; 7(2): 237–242

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6181890/

■ Genetics of autosomal recessive polycystic kidney disease and its differential diagnoses

Carsten Bergmann

Front Pediatr. 2017; 5: 221

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5811498/

■ Practical approaches to the management of autosomal dominant polycystic kidney disease patients in the era of tolvaptan

Roman-Ulrich Müller, Christian S Haas, John A Sayer

Clin Kidney J. 2018 Feb; 11(1): 62–69

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5798152/

■ Infected renal cyst presented with pleural effusion in a woman with autosomal dominant polycystic kidney disease

Ester Casillas-Sagrado, Victor Burguera, Maria Eugenia Rioja-Martín, Maite Rivera-Gorrín

Clin Kidney J. 2018 Apr; 11(2): 204–206

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5888413/

■ Recommendations for the use of tolvaptan in autosomal dominant polycystic kidney disease: a position statement on behalf of the ERA-EDTA Working Groups on Inherited Kidney Disorders and European Renal Best Practice

R T Gansevoort M A Thomas, B Henrik et al

Nephrology Dialysis Transplantation 2016, vol 31 (3): 337-348

https://academic.oup.com/ndt/article/31/3/337/2460159

■ Resultado do transplante renal com doador portador de doença renal policística

Migone, Silvia Regina da Cruz et al.

Bras. Nefrol., Sept 2016, vol.38, no.3, p.379-382

http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0101-28002016000300379&lng=en&nrm=iso&tlng=pt

http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0101-28002016000300379&lng=en&nrm=iso&tlng=en (english)

■ Unexpected relevance of the hallmarks of cancer to the pathogenesis of polycystic kidney disease

Tamina Seeger-Nukpezah, Daniel M. Geynisman, Anna S. Nikonova et al

Rev Nephrol. 2015 Sep; 11(9): 515–534

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5902186/

■ Doença renal policística autossômica dominante em pacientes em hemodiálise no sul do Brasil

Alves, Everton Fernando et al.

J Bras Nefrol, Mar 2014, vol.36, no.1, p.18-2

http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0101-28002014000100018&lng=en&nrm=iso

■ Autosomal dominant polycystic kidney disease

A Srivastava, N Patel

Am Fam Physician 2014, vol 90 (5): 303-307

https://www.aafp.org/afp/2014/0901/p303.html

■ Hereditary polycystic kidney disease: genetic diagnosis and counseling.

Whittle, Martin and Simões, Ricardo

Rev. Assoc. Med. Bras., 2014, vol.60, no.2, p.98-102. ISSN 0104-4230

http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0104-42302014000200098&lng=en&nrm=iso

■ Pain determinants of pain in autosomal dominant polycystic kidney disease

Nishiura, José Luiz, Eloi, Samara Rodrigues Moreira and Heilberg, Ita Pfeferman

Bras. Nefrol., Sept 2013, vol.35, no.3, p.242-243

http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0101-28002013000300012&lng=en&nrm=iso&tlng=en

■ Ansiedade, depressão e qualidade de vida em pacientes com glomerulonefrite familiar ou doença renal policística autossômica dominante

Barros, Bruna Paes de et al.

Bras. Nefrol., Jun 2011, vol.33, no.2, p.120-128

http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0101-28002011000200002&lng=en&nrm=iso

■ Tradução, adaptação cultural e aplicação de um questionário de dor para pacientes com doença renal policística.

Eloi, Samara Rodrigues Moreira, Nishiura, José Luiz and Heilberg, Ita Pfeferman

Bras. Nefrol., Dez 2010, vol.32, no.4, p.393-407

http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0101-28002010000400009&lng=en&nrm=iso

Dias, Natasha Favoretto et al. Aspectos clínicos da doença renal policística autossômica recessiva DRPAR. J. Bras. Nefrol., Set 2010, vol.32, no.3, p.263-267

http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0101-28002010000300007&lng=en&nrm=iso

■ Aneurismas das artérias coronárias: uma rara manifestação da doença renal policística autossômica dominante

Velásquez, Alejandro Sánchez et al.

Rev. Bras. Cardiol. Invasiva, 2010, vol.18, no.4, p.476-478

http://www.scielo.br/scielo.php?script=sci_arttext&pid=S2179-83972010000400020&lng=en&nrm=iso