Increased Meal Size but Reduced Meal-Stimulated Plasma Cholecystokinin Concentrations in Women With Obesity

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

Increased Meal Size but Reduced Meal-Stimulated Plasma Cholecystokinin Concentrations in Women With Obesity. / Geary, Nori; Asarian, Lori; Graf, Gwendolyn; Gobbi, Susanna; Tobler, Philippe N.; Rehfeld, Jens F.; Leeners, Brigitte.

I: Endocrinology, Bind 164, Nr. 1, bqac192, 2023.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Geary, N, Asarian, L, Graf, G, Gobbi, S, Tobler, PN, Rehfeld, JF & Leeners, B 2023, 'Increased Meal Size but Reduced Meal-Stimulated Plasma Cholecystokinin Concentrations in Women With Obesity', Endocrinology, bind 164, nr. 1, bqac192. https://doi.org/10.1210/endocr/bqac192

APA

Geary, N., Asarian, L., Graf, G., Gobbi, S., Tobler, P. N., Rehfeld, J. F., & Leeners, B. (2023). Increased Meal Size but Reduced Meal-Stimulated Plasma Cholecystokinin Concentrations in Women With Obesity. Endocrinology, 164(1), [bqac192]. https://doi.org/10.1210/endocr/bqac192

Vancouver

Geary N, Asarian L, Graf G, Gobbi S, Tobler PN, Rehfeld JF o.a. Increased Meal Size but Reduced Meal-Stimulated Plasma Cholecystokinin Concentrations in Women With Obesity. Endocrinology. 2023;164(1). bqac192. https://doi.org/10.1210/endocr/bqac192

Author

Geary, Nori ; Asarian, Lori ; Graf, Gwendolyn ; Gobbi, Susanna ; Tobler, Philippe N. ; Rehfeld, Jens F. ; Leeners, Brigitte. / Increased Meal Size but Reduced Meal-Stimulated Plasma Cholecystokinin Concentrations in Women With Obesity. I: Endocrinology. 2023 ; Bind 164, Nr. 1.

Bibtex

@article{b09eaeb18aba4b7c87431d56a3b36171,
title = "Increased Meal Size but Reduced Meal-Stimulated Plasma Cholecystokinin Concentrations in Women With Obesity",
abstract = "To better understand the physiological basis of obesity in women, we investigated whether obesity or menstrual cycle phase affects laboratory test-meal size or meal-stimulated plasma cholecystokinin (CCK) concentration. Women with healthy weight (body mass index [BMI] of 18.5-24.9 kg/m(2), N = 16) or obesity (BMI 30-39.9 kg/m(2), N = 20) were tested once in the late-follicular or peri-ovulatory phase (LF/PO) and once in the mid-luteal phase (ML). Meals of ham sandwiches were offered and blood was sampled. Menstrual cycle phases were verified with participants' reports of menses and measurements of progesterone and luteinizing hormone (LH) concentrations. Women with obesity ate significantly larger meals than women with healthy weight, (mean, 711 [95% CI, 402-1013] kJ, P = 0.001, during the LF/PO and 426 [105-734] kJ, P = 0.027, larger during the ML). Women with healthy weight ate smaller meals during LF/PO than ML (decrease, 510 [192-821 kJ], P = 0.008), but women with obesity did not (decrease, 226 [-87-542] kJ, P = 0.15). CCK concentrations 18 to 30 minutes after meal onset were lower in women with obesity than in women with healthy weight during LF/PO (3.6 [3.1-4.1] vs 6.1 [4.5-7.7] pmol/L; P = 0.004), but not during ML, with a significant interaction effect (1.8 [1.2-2.4] pmol/L, P = 0.048). Women with obesity consumed larger meals than women with healthy weight but displayed reduced meal-stimulated plasma CCK concentrations. These data are consistent with the hypothesis that a defect in CCK secretion compromises satiation in obese women and contributes to the development or maintenance of obesity.",
keywords = "satiety, satiation, appetite, energy homeostasis, cholecystokinin, APPETITE CONTROL IMPLICATIONS, GLUCAGON-LIKE PEPTIDE-1, BODY-MASS INDEX, RECEPTOR ANTAGONIST, MENSTRUAL-CYCLE, WEIGHT-LOSS, FOOD-INTAKE, DIETARY RESTRAINT, OVARIAN HORMONES, EATING BEHAVIOR",
author = "Nori Geary and Lori Asarian and Gwendolyn Graf and Susanna Gobbi and Tobler, {Philippe N.} and Rehfeld, {Jens F.} and Brigitte Leeners",
year = "2023",
doi = "10.1210/endocr/bqac192",
language = "English",
volume = "164",
journal = "Journal of Clinical Endocrinology and Metabolism",
issn = "0013-7227",
publisher = "Oxford University Press",
number = "1",

}

RIS

TY - JOUR

T1 - Increased Meal Size but Reduced Meal-Stimulated Plasma Cholecystokinin Concentrations in Women With Obesity

AU - Geary, Nori

AU - Asarian, Lori

AU - Graf, Gwendolyn

AU - Gobbi, Susanna

AU - Tobler, Philippe N.

AU - Rehfeld, Jens F.

AU - Leeners, Brigitte

PY - 2023

Y1 - 2023

N2 - To better understand the physiological basis of obesity in women, we investigated whether obesity or menstrual cycle phase affects laboratory test-meal size or meal-stimulated plasma cholecystokinin (CCK) concentration. Women with healthy weight (body mass index [BMI] of 18.5-24.9 kg/m(2), N = 16) or obesity (BMI 30-39.9 kg/m(2), N = 20) were tested once in the late-follicular or peri-ovulatory phase (LF/PO) and once in the mid-luteal phase (ML). Meals of ham sandwiches were offered and blood was sampled. Menstrual cycle phases were verified with participants' reports of menses and measurements of progesterone and luteinizing hormone (LH) concentrations. Women with obesity ate significantly larger meals than women with healthy weight, (mean, 711 [95% CI, 402-1013] kJ, P = 0.001, during the LF/PO and 426 [105-734] kJ, P = 0.027, larger during the ML). Women with healthy weight ate smaller meals during LF/PO than ML (decrease, 510 [192-821 kJ], P = 0.008), but women with obesity did not (decrease, 226 [-87-542] kJ, P = 0.15). CCK concentrations 18 to 30 minutes after meal onset were lower in women with obesity than in women with healthy weight during LF/PO (3.6 [3.1-4.1] vs 6.1 [4.5-7.7] pmol/L; P = 0.004), but not during ML, with a significant interaction effect (1.8 [1.2-2.4] pmol/L, P = 0.048). Women with obesity consumed larger meals than women with healthy weight but displayed reduced meal-stimulated plasma CCK concentrations. These data are consistent with the hypothesis that a defect in CCK secretion compromises satiation in obese women and contributes to the development or maintenance of obesity.

AB - To better understand the physiological basis of obesity in women, we investigated whether obesity or menstrual cycle phase affects laboratory test-meal size or meal-stimulated plasma cholecystokinin (CCK) concentration. Women with healthy weight (body mass index [BMI] of 18.5-24.9 kg/m(2), N = 16) or obesity (BMI 30-39.9 kg/m(2), N = 20) were tested once in the late-follicular or peri-ovulatory phase (LF/PO) and once in the mid-luteal phase (ML). Meals of ham sandwiches were offered and blood was sampled. Menstrual cycle phases were verified with participants' reports of menses and measurements of progesterone and luteinizing hormone (LH) concentrations. Women with obesity ate significantly larger meals than women with healthy weight, (mean, 711 [95% CI, 402-1013] kJ, P = 0.001, during the LF/PO and 426 [105-734] kJ, P = 0.027, larger during the ML). Women with healthy weight ate smaller meals during LF/PO than ML (decrease, 510 [192-821 kJ], P = 0.008), but women with obesity did not (decrease, 226 [-87-542] kJ, P = 0.15). CCK concentrations 18 to 30 minutes after meal onset were lower in women with obesity than in women with healthy weight during LF/PO (3.6 [3.1-4.1] vs 6.1 [4.5-7.7] pmol/L; P = 0.004), but not during ML, with a significant interaction effect (1.8 [1.2-2.4] pmol/L, P = 0.048). Women with obesity consumed larger meals than women with healthy weight but displayed reduced meal-stimulated plasma CCK concentrations. These data are consistent with the hypothesis that a defect in CCK secretion compromises satiation in obese women and contributes to the development or maintenance of obesity.

KW - satiety

KW - satiation

KW - appetite

KW - energy homeostasis

KW - cholecystokinin

KW - APPETITE CONTROL IMPLICATIONS

KW - GLUCAGON-LIKE PEPTIDE-1

KW - BODY-MASS INDEX

KW - RECEPTOR ANTAGONIST

KW - MENSTRUAL-CYCLE

KW - WEIGHT-LOSS

KW - FOOD-INTAKE

KW - DIETARY RESTRAINT

KW - OVARIAN HORMONES

KW - EATING BEHAVIOR

U2 - 10.1210/endocr/bqac192

DO - 10.1210/endocr/bqac192

M3 - Journal article

C2 - 36423205

VL - 164

JO - Journal of Clinical Endocrinology and Metabolism

JF - Journal of Clinical Endocrinology and Metabolism

SN - 0013-7227

IS - 1

M1 - bqac192

ER -

ID: 343213609