Reduced bone mineral density in the first year after total pancreatectomy with islet autotransplantation (TPIAT)

Pancreatology ◽  
2021 ◽  
Author(s):  
Jillian K. Wothe ◽  
Robert Aidoo ◽  
Kendall R. McEachron ◽  
Tasma Harindhanavudhi ◽  
Guru Trikudanathan ◽  
...  
2016 ◽  
Vol 21 ◽  
pp. 241-249 ◽  
Author(s):  
Ewa Nowacka-Cieciura ◽  
Anna Sadowska ◽  
Marek Pacholczyk ◽  
Andrzej Chmura ◽  
Olga Tronina ◽  
...  

2020 ◽  
Vol 9 (6) ◽  
pp. 1830 ◽  
Author(s):  
Fernando Guerrero-Pérez ◽  
Anna Casajoana ◽  
Carmen Gómez-Vaquero ◽  
Nuria Virgili ◽  
Rafael López-Urdiales ◽  
...  

There is scant evidence of the long-term effects of bariatric surgery on bone mineral density (BMD). We compared BMD changes in patients with severe obesity and type 2 diabetes (T2D) 5 years after randomization to metabolic gastric bypass (mRYGB), sleeve gastrectomy (SG) and greater curvature plication (GCP). We studied the influence of first year gastrointestinal hormone changes on final bone outcomes. Forty-five patients, averaging 49.4 (7.8) years old and body mass index (BMI) 39.4 (1.9) kg/m2, were included. BMD at lumbar spine (LS) was lower after mRYGB compared to SG and GCP: 0.89 [0.82;0.94] vs. 1.04 [0.91;1.16] vs. 0.99 [0.89;1.12], p = 0.020. A higher percentage of LS osteopenia was present after mRYGB 78.6% vs. 33.3% vs. 50.0%, respectively. BMD reduction was greater in T2D remitters vs. non-remitters. Weight at fifth year predicted BMD changes at the femoral neck (FN) (adjusted R2: 0.3218; p = 0.002), and type of surgery (mRYGB) and menopause predicted BMD changes at LS (adjusted R2: 0.2507; p < 0.015). In conclusion, mRYGB produces higher deleterious effects on bone at LS compared to SG and GCP in the long-term. Women in menopause undergoing mRYGB are at highest risk of bone deterioration. Gastrointestinal hormone changes after surgery do not play a major role in BMD outcomes.


Urology ◽  
2007 ◽  
Vol 70 (1) ◽  
pp. 122-126 ◽  
Author(s):  
Christopher W. Ryan ◽  
Dezheng Huo ◽  
James W. Stallings ◽  
Ronald L. Davis ◽  
Tomasz M. Beer ◽  
...  

2004 ◽  
Vol 36 (2) ◽  
pp. 285-286 ◽  
Author(s):  
Jose Luis Merino ◽  
Jose Luis Teruel ◽  
Milagros Fernandez ◽  
Maite Rivera ◽  
M. Carmen Caballero ◽  
...  

1997 ◽  
Vol 82 (8) ◽  
pp. 2386-2390 ◽  
Author(s):  
Hermann M. Behre ◽  
Sabine Kliesch ◽  
Eckhard Leifke ◽  
Thomas M. Link ◽  
Eberhard Nieschlag

In both men and women, a decrease in bone mineral density (BMD) is a major symptom of hypogonadism. Although the effects of estrogens on osteoporosis in women are well documented, comparatively little is known about the effects of long term testosterone substitution on BMD in hypogonadal men. Therefore, we studied BMD in 72 hypogonadal patients (37 men with primary and 35 men with secondary hypogonadism) under testosterone substitution therapy that continued for up to 16 yr. Thirty-two of these men were also seen before initiation of therapy. At annual intervals, trabecular BMD of the lumbar spine was measured by quantitative computed tomography, a true volumetric and reproducible method for long term serial BMD measurements. Serum levels of testosterone increased to the normal range in all androgen-treated hypogonadal men. The most significant increase in BMD was seen during the first year of testosterone treatment in previously untreated patients, when BMD increased from 95.2 ± 5.9 to 120.0 ± 6.1 mg/cm3 hydroxyapatite (mean ± se). Long term testosterone treatment maintained BMD in the age-dependent reference range in all 72 hypogonadal men, independent of the type of hypogonadism. Transdermal testosterone patches applied to the scrotum were as effective in normalizing BMD as im testosterone enanthate injections. In summary, testosterone therapy increases BMD in hypogonadal men regardless of age. The greatest increase is seen during the first year of treatment in previously untreated patients with low initial BMD. In hypogonadal men, BMD can be normalized and maintained in the normal range by continuous, long term testosterone substitution.


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