Enhanced endometrial proliferation correlates obesity to type-I (estrogen-dependent) endometrial cancer (EC). Our aim was to distinguish obese women (without EC) with differing endometrial proliferation. Endometrial and blood samples were obtained from normal-weight and obese women without EC. Type-I EC samples were obtained from obese patients. On measuring endometrial proliferation (Ki67 and phosphorylated histone H3 (p-H3)), two groups of obese women without EC were identified: obese High Proliferating (O HP ) and obese Low Proliferating (O LP ). Increased Ki67 (88.5%, Po0.001), p-H3 (62.6%, Po0.01), 17b-estradiol/ progesterone ratio (46.3%, Po0.01) and endometrial estrogen receptor alpha (ERa) (82.2%, Po0.001) were observed in O HP compared with O LP patients. ECs possessed similar ERa and enhanced proliferation as O HP , suggesting that O HP women are at higher risk of type-I EC. O LP women were indistinguishable from normal-weight women regarding these determinants of endometrial proliferation, ERa and 17b-estradiol/progesterone ratio. Our data may further define the obesity phenotype in regards to type-I EC risk and may help identify obese women more susceptible to develop type-I EC, allowing early intervention and a potential reduction in mortality.