Background: Obesity has become an increasinglyworrisome reality. Avery-low-calorie ketogenic diet (VLCKD) represents a promising option bywhich to achieve significantweight loss. This study sought to evaluate the effectiveness of VLCKD on metabolic parameters and hormonal profiles of obese male patients. Methods: We enrolled 40 overweight/obese men who consumed VLCKD for at least eight weeks. Body weight, waist circumference, fasting glucose, insulin, total cholesterol, high-density lipoprotein, triglycerides, creatinine, uric acid, aspartate aminotransferase, alanine aminotransferase, vitamin D, luteinizing hormone (LH), total testosterone (TT), and prostate-specific antigen (PSA)were calculated before and after VLCKD consumption. We additionally determined the homeostasismodel assessment index and low-density lipoprotein (LDL) values. Results: AfterVLCKD(13.50.83weeks), themean bodyweight loss was 21.05 1.44 kg; the glucose homeostasis and lipid profile were improved significantly; serum vitamin D, LH, and TT levels were increased and the PSA levels were decreased significantly as compared with pretreatment values. These results are of interest since obesity can lead to hypogonadism and in turn, testosterone deficiency is associatedwith impaired glucose homeostasis,metabolic syndrome, and diabetes mellitus. Moreover, a close relationship between obesity, insulin resistance, and/or hyperinsulinemia and increased prostate volume has been reported, with a consequent greater risk of developing lower urinary tract symptoms. Conclusions: VLCKDis an effective tool against obesity and could be a noninvasive, rapid, and valid means to treat obese patients with metabolic hypogonadism and lower urinary tract symptoms.

Effectiveness of a very-low-calorie ketogenic diet on testicular function in overweight/obese men

Mongioì LM;Cimino L;Condorelli RA;Magagnini MC;Barbagallo F;Cannarella R;La Vignera S;Calogero AE
2020-01-01

Abstract

Background: Obesity has become an increasinglyworrisome reality. Avery-low-calorie ketogenic diet (VLCKD) represents a promising option bywhich to achieve significantweight loss. This study sought to evaluate the effectiveness of VLCKD on metabolic parameters and hormonal profiles of obese male patients. Methods: We enrolled 40 overweight/obese men who consumed VLCKD for at least eight weeks. Body weight, waist circumference, fasting glucose, insulin, total cholesterol, high-density lipoprotein, triglycerides, creatinine, uric acid, aspartate aminotransferase, alanine aminotransferase, vitamin D, luteinizing hormone (LH), total testosterone (TT), and prostate-specific antigen (PSA)were calculated before and after VLCKD consumption. We additionally determined the homeostasismodel assessment index and low-density lipoprotein (LDL) values. Results: AfterVLCKD(13.50.83weeks), themean bodyweight loss was 21.05 1.44 kg; the glucose homeostasis and lipid profile were improved significantly; serum vitamin D, LH, and TT levels were increased and the PSA levels were decreased significantly as compared with pretreatment values. These results are of interest since obesity can lead to hypogonadism and in turn, testosterone deficiency is associatedwith impaired glucose homeostasis,metabolic syndrome, and diabetes mellitus. Moreover, a close relationship between obesity, insulin resistance, and/or hyperinsulinemia and increased prostate volume has been reported, with a consequent greater risk of developing lower urinary tract symptoms. Conclusions: VLCKDis an effective tool against obesity and could be a noninvasive, rapid, and valid means to treat obese patients with metabolic hypogonadism and lower urinary tract symptoms.
2020
very low calorie ketogenic diet, glucose homeostasis, lipid profile, vitamin D, testosterone
File in questo prodotto:
File Dimensione Formato  
518_Mongioì_VCLKD-Testis_Nutrients_2020.pdf

accesso aperto

Tipologia: Versione Editoriale (PDF)
Dimensione 453.21 kB
Formato Adobe PDF
453.21 kB Adobe PDF Visualizza/Apri

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11769/487805
Citazioni
  • ???jsp.display-item.citation.pmc??? 13
  • Scopus 26
  • ???jsp.display-item.citation.isi??? 24
social impact