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1.
J Endocrinol Invest ; 44(10): 2195-2202, 2021 Oct.
Article in English | MEDLINE | ID: mdl-33569721

ABSTRACT

PURPOSE: Acromegaly is associated with many comorbidities and increased mortality. The first-line treatment is transsphenoidal surgery. However, many patients also need adjuvant drug treatment after surgery. Somatostatin analog (SSA), which suppresses GH secretion by somatotrophs by binding to the SSTR2 receptor, is the first choice. Nevertheless, 50% of patients are partially or totally resistant to SSA, so predictive factors of response are helpful to individualize drug treatment. 68GaDOTATATE PET/CT has emerged as the gold-standard method in the diagnosis and follow-up of gastroenteropancreatic neuroendocrine tumors, which also express SSTR. Our objective was to evaluate whether 68Ga-DOTATATE uptake (SUV max) at the pituitary region of patients on SSA therapy would be useful as a drug response predictor without the need of tumoral tissue. METHODS: Fifteen acromegalics patients on SSA treatment for at least 6 months were underwent to 68Ga-DOTATATE PET/CT at the nuclear medicine service. There was an SSA complete response group (n = 5), defined as GH < 1 µg/L and IFG-1 in the normal range for gender and age, and a group that did not meet these criteria (n = 10). RESULTS: As a result, we did not find out a significantly higher SUV max in the complete response group (p = 0.0576) to SSA. However, we found a significant inverse relationship between postoperative GH values and the SUVmax at the sella turcica (p = 0.0188), probably reflecting tumor SSTR2 expression. CONCLUSION: Thus, after this initial evaluation, 68GaDOTATATE PET/CT should be better studied to assess its usefulness in the follow-up of acromegalic patients.


Subject(s)
Acromegaly/pathology , Organometallic Compounds/metabolism , Pituitary Neoplasms/pathology , Positron Emission Tomography Computed Tomography/methods , Somatostatin/therapeutic use , Acromegaly/diagnostic imaging , Acromegaly/drug therapy , Acromegaly/metabolism , Adult , Aged , Cross-Sectional Studies , Female , Follow-Up Studies , Hormones/therapeutic use , Humans , Male , Middle Aged , Pituitary Neoplasms/diagnostic imaging , Pituitary Neoplasms/drug therapy , Pituitary Neoplasms/metabolism , Prognosis , Somatostatin/analogs & derivatives , Young Adult
2.
Pituitary ; 23(2): 120-128, 2020 Apr.
Article in English | MEDLINE | ID: mdl-31728906

ABSTRACT

OBJECTIVE: To evaluate the maternal-fetal outcomes of CAB-induced pregnancies in patients with prolactinoma in a large cohort. METHODS: The prevalence of tumor growth, miscarriage, preterm, low birth weight, congenital malformations and impairment in neuropsychological development in children among women treated with CAB were assessed in a Brazilian multicentre retrospective observational study, RESULTS: We included 194 women with a mean age of 31 (17-45) years, 43.6% presenting microadenomas and 56.4% macroadenomas, at prolactinoma diagnosis. In 233 pregnancies, CAB was withdrawn in 89%, after pregnancy confirmation. Symptoms related to tumor growth occurred in 25 cases, more frequently in macroadenomas. The overall miscarriage rate was 11%, although higher in the subgroup of patients with CAB maintainance after pregnancy confirmation (38% vs. 7.5%). Amongst the live-birth deliveries, preterm occurred in 12%, low birth weight in 6% and congenital malformations in 4.3%. Neuropsychological development impairment was reported in 7% of cases. CONCLUSIONS: Our findings confirm previous results of safety in maternal and fetal outcomes in CAB-induced pregnancies; nevertheless, CAB maintenance after pregnancy confirmation was associated with higher miscarriage rate; result that must be further confirmed.


Subject(s)
Cabergoline/therapeutic use , Dopamine Agonists/therapeutic use , Prolactinoma/pathology , Abortion, Spontaneous/pathology , Adolescent , Adult , Aged , Female , Humans , Hyperprolactinemia/pathology , Middle Aged , Pregnancy , Pregnancy Complications, Neoplastic , Retrospective Studies , Young Adult
3.
Am J Med Genet ; 41(4): 444-5, 1991 Dec 15.
Article in English | MEDLINE | ID: mdl-1776634

ABSTRACT

We report on a 5-year-old girl with a male karyotype (46,XY), severe psychomotor and physical retardation, minor anomalies, and female external genitalia with a blindly ending vagina. She has normal adrenal function, prepubertal serum gonadotropin and testosterone levels, which did not rise after hCG stimulation. On abdominal exploration no gonads were found, and only mesonephric and Müllerian remnants. She was HY positive, and no deletion was detected in the Y chromosome using 5 different probes. Although a genetic defect is not excluded, pregnancy complications suggest an environmental insult to the developing testes.


Subject(s)
Testis/abnormalities , Child, Preschool , DNA Probes , Disorders of Sex Development/genetics , Genitalia/abnormalities , Humans , Male , Phenotype , Y Chromosome
4.
Braz J Med Biol Res ; 24(2): 149-56, 1991.
Article in English | MEDLINE | ID: mdl-1823227

ABSTRACT

1. The function of a Y human chromosomal DNA sequence was evaluated. The Y-5 probe was isolated from a flow-sorted chromosome library and detects Y-specific sequences. 2. The Y-5 probe and other Y-specific probes were used to analyze an XX male patient without ambiguous genitalia. 3. DNA sequences from the short arm of the chromosome Y that were detected with pDP1007 and pDP105 in the patient's genome explain the testis differentiation observed in this case. 4. Failure of the patient's DNA to hybridize to the Y-5 probe shows that the primitive gonads can differentiate into testes even in the absence of this chromosome region. In contrast, a gene controlling spermatogenesis may exist in this region because the patient is azoospermic.


Subject(s)
DNA Probes , Sex Chromosome Aberrations , Sex Differentiation , Y Chromosome/physiology , Adolescent , Blotting, Southern , Humans , Karyotyping , Male , Nucleic Acid Hybridization
5.
Braz. j. med. biol. res ; 24(2): 149-56, 1991. tab
Article in English | LILACS | ID: lil-99449

ABSTRACT

The function of a Y human chromosomal DNA sequence was evaluated. The Y-5 probe was isolated from a flow-sorted chromosome library and detects Y-specific sequences. The Y-5 probe and other T-specific probes were used to analyze an XX male patient without ambiguous genitalia. DNA sequences from the short arm of the chromosome Y that were detected with pDP1007 and DP105 in the patient's genome explain the testis differentation observed in this case. Failure of the patient's DNA to hybridize to the Y-5 probe shows that the primitive gonads can differentiate into testes even in the absence of this chromosome region. In contrast, a gene controlling spermatogenesis may exist in this region because the patient azoospermic


Subject(s)
Humans , Male , Adolescent , DNA Probes , Sex Chromosome Aberrations , Sex Determination Analysis , Y Chromosome/physiology , Blotting, Southern , Karyotyping , Nucleic Acid Hybridization
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