scholarly journals Expression Analysis of Dopamine Receptor Subtypes in Normal Human Pituitaries, Nonfunctioning Pituitary Adenomas and Somatotropinomas, and the Association between Dopamine and Somatostatin Receptors with Clinical Response to Octreotide-LAR in Acromegaly

2009 ◽  
Vol 94 (6) ◽  
pp. 1931-1937 ◽  
Author(s):  
Leonardo Vieira Neto ◽  
Evelyn de O. Machado ◽  
Raul M. Luque ◽  
Giselle F. Taboada ◽  
Jorge B. Marcondes ◽  
...  
2008 ◽  
Vol 52 (8) ◽  
pp. 1288-1295 ◽  
Author(s):  
Leonardo Vieira Neto ◽  
Giselle Fernandes Taboada ◽  
Mônica Roberto Gadelha

We present two acromegalic patients in which clinical and molecular data are discussed in regard to their ability to predict long term octreotide LAR® therapy response. Case reports: Patient 1: female, 36 years old at diagnosis. Basal GH and IGF-I at diagnosis were 133 ng/mL and 181% above the upper limit of reference values (ULRV), respectively. Growth hormone during acute test with subcutaneous octreotide decreased from 133 to 13 ng/mL. Patient started on primary octreotide LAR® therapy (20mg q28 days) and achieved biochemical parameters of disease control after 6 months. Molecular analysis of tumor fragments: gsp +; quantitative analysis of SSTR (somatostatin receptor) and DR (dopamine receptor) mRNA - SSTR2 23954; SSTR5 2407; DR2 total 17016 copies. Patient 2: male, 38 years old at diagnosis. Basal GH and IGF-I at diagnosis were 120 ng/mL and 114% ULRV, respectively. Patient underwent non-curative trans-sphenoidal surgery. Post-operative GH and IGF-I were 112 ng/mL and 137% ULRV, respectively. Growth hormone during acute test with subcutaneous octreotide decreased from 112 to 7 ng/mL. Octreotide LAR® therapy (20 mg q28 days) was then initiated. After 6 months of treatment, patient did not attain biochemical control of disease and displayed increased tumor volume. Molecular analysis of tumor fragments: gsp not done; quantitative analysis of SSTR and DR mRNA - SSTR2 416; SSTR5 3767; DR2 total 3439 copies. In conclusion, these two cases illustrate how laboratory data can be conflicting as predictors of octreotide LAR® responsiveness and how molecular analysis of tumor fragments can help explain different behaviors in clinically similar patients.


2010 ◽  
Vol 52 (4) ◽  
pp. 336-343
Author(s):  
Noriaki Koshikawa ◽  
Katsunori Tomiyama ◽  
John L. Waddington

1986 ◽  
Vol 7 (5) ◽  
pp. 357-361 ◽  
Author(s):  
Jacquelyn M. Henry ◽  
Charles R. Filburn ◽  
James A. Joseph ◽  
George S. Roth

1992 ◽  
Vol 20 ◽  
pp. 27-32 ◽  
Author(s):  
Pierre Sokoloff ◽  
Marie-Pascalle Martres ◽  
Bruno Giros ◽  
Marie-Louise Bouthenet ◽  
Jean-Charles Schwartz

2009 ◽  
Vol 65 (1) ◽  
pp. 53-63 ◽  
Author(s):  
Padmesh S. Rajput ◽  
Geetanjali Kharmate ◽  
Rishi K. Somvanshi ◽  
Ujendra Kumar

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