CIRCULATING TOTAL LEPTIN, LEPTIN RECEPTOR AND FREE LEPTIN INDEX LEVELS IN CHRONIC MYELOMONOCYTIC LEUKEMIA: A CROSS-SECTIONAL STUDY
Author(s): ,
Maria Dalamaga
Affiliations:
Clinical Biochemistry,University of Athens, School of Medicine, Attikon General University Hospital,Athens,Greece;Clinical Biochemistry,University of Athens, School of Medicine, Attikon General University Hospital,Athens,Greece
,
Antigoni Lekka
Affiliations:
Laboratory of Hematology,NIMTS Hospital,Athens,Greece
,
Maria Triantafilli
Affiliations:
Laboratory of Hematology,NIMTS Hospital,Athens,Greece
,
George Sotiropoulos
Affiliations:
Laboratory of Hematology,NIMTS Hospital,Athens,Greece
,
John Chamberland
Affiliations:
Division of Endocrinology, Diabetes and Metabolism, Beth Israel Deaconess Medical Center,Harvard Medical School,Boston,United States
,
Konstantinos Karmaniolas
Affiliations:
Department of Internal Medicine,NIMTS Hospital,Athens,Greece
,
Lambros Tzianoumis
Affiliations:
Hematologic Clinic,Ygeias Melathron, TYPET,Athens,Greece
Christos Mantzoros
Affiliations:
Division of Endocrinology, Diabetes and Metabolism, Beth Israel Deaconess Medical Center,Harvard Medical School,Boston,United States
EHA Learning Center. Lekka A. Jun 12, 2015; 102593
Antigoni Lekka
Antigoni Lekka

Access to EHA Members only content is an EHA membership benefit. Click here to join EHA or renew your membership here.


Abstract
Discussion Forum (0)
Rate & Comment (0)
Abstract: PB1841

Type: Publication Only

Background
Recent evidence suggests that overweight/obesity may be implicated in the etiology of hematologic malignancies, including myelogenous leukemia and myelodysplastic syndromes. A strong asociation of overweight/obesity with insulin resistance, characterized by hyperinsulinemia, has been well documented. There is evidence that insulin resistance is implicated in several malignancies associated with excess body weight. Leptin and, particularly, free leptin, the biologically significant form of leptin, reflecting accurately the body fat mass, regulate glucose and lipid metabolism by ameliorating insulin sensitivity and decreasing intracellular lipids. 

Aims
In this cross-sectional study, we investigated the potential association of leptin and free leptin with chronic myelomonocytic leukemia (CMML), a hematologic malignancy combining proliferative and dysplastic features, after adjusting for a potential confounding effect of age,gender, date of diagnosis (matching factors) a well as withbody mass index (BMI), family history of lymphohematopoietic cancer (LHC) and serum insulin.

Methods

Blood samples were collected from 14 cases with incident, histologically confirmed CMML and 70 healthy controls (in an analogy of one patient versus five healthy controls) who came for an annual check-up examination without any neoplastic and infectious conditions, matched on gender, age and year/month of diagnosis (±1 month) between 2004-2012. Informed consent was obtained from all study participants. Serum leptin and insulin were determined by radioimmunoassay (Linco Research Institute St Louis MO, and Millipore Co Billerica, MA respectively). Serum leptin receptor levels (sOB-R) levels were measured using a commercially available ELISA (BioVendor R&D, Brno, Czech Republic). Free Leptin Index (FLI) was calculated as the ratio of leptin to sOBR. The statistical analysis of the data was performed using IBM-SPSS® version 22 for Windows.



Results

CMML cases presented significantly higher height and weight than control subjects (p<0.001), while differences of BMI were only of borderline significance (p=0.10). Serum insulin was significantly higher in cases than controls (p=0.05). CMML cases exhibited a significant total and free hypoleptinemia in comparison to controls (total leptin in patients with CMML: 13.2 ± 16.3 ng/mL versus controls 24 ± 21.1 ng/mL, p=0.005; FLI in patients with CMML: 0.81 ± 1.6 versus controls: 2.84 ± 5.4, p=0.04). Moreover, CMML cases exhibited significantly lower serum levels of sOB-R than controls (p=0.04). In multivariate analysis, subjects with total and free hypoleptinemia presented significantly higher odds for CMML after adjusting for age, gender, date of diagnosis, BMI, family history of LHC and serum insulin levels.  



Summary
This study raises the hypothesis that leptin which reflects overall fat mass and insulin may be associated with CMML. Leptin’s major physiological role is to signal inadequate rather than excess energy stores, and hypoleptinemia found in a small but significant percentage of obese humans is associated with hyperinsulinemia and impaired T-cell function. Further mechanistic, interventional and epidemiological studies are needed to confirm these findings and to explore whether leptin may mediate the effect of body fat distribution on insulin resistance and leukemogenesis risk.

Keyword(s): Chronic myelomonocytic leukemia, Myeloproliferative disorder, Obesity
Code of conduct/disclaimer available in General Terms & Conditions
Anonymous User Privacy Preferences

Strictly Necessary Cookies (Always Active)

MULTILEARNING platforms and tools hereinafter referred as “MLG SOFTWARE” are provided to you as pure educational platforms/services requiring cookies to operate. In the case of the MLG SOFTWARE, cookies are essential for the Platform to function properly for the provision of education. If these cookies are disabled, a large subset of the functionality provided by the Platform will either be unavailable or cease to work as expected. The MLG SOFTWARE do not capture non-essential activities such as menu items and listings you click on or pages viewed.


Performance Cookies

Performance cookies are used to analyse how visitors use a website in order to provide a better user experience.



Google Analytics is used for user behavior tracking/reporting. Google Analytics works in parallel and independently from MLG’s features. Google Analytics relies on cookies and these cookies can be used by Google to track users across different platforms/services.


Save Settings