Rönnemaa T, Karonen S L, Rissanen A, Koskenvuo M, Koivisto V A
University of Turku, Research and Development Center of Social Insurance Institution, Finland.
Ann Intern Med. 1997 Jan 1;126(1):26-31. doi: 10.7326/0003-4819-126-1-199701010-00004.
Plasma levels of leptin, the recently discovered satiety hormone, are associated with adiposity in humans.
To determine whether genetic factors or body fat distribution affect the association between leptin levels and obesity.
23 healthy identical twin pairs (9 male pairs and 14 female pairs, 33 to 59 years of age) who were discordant for obesity (average weight difference, 18 kg).
Fasting plasma leptin levels were measured by radioimmunoassay. Distribution of abdominal fat into visceral and subcutaneous compartments was estimated by use of magnetic resonance imaging.
Plasma leptin levels were threefold higher in obese twins than in lean twins (mean +/- SD, 18.7 +/- 12.5 micrograms/L compared with 6.4 +/- 4.8 micrograms/L; P < 0.001); a similar difference was seen when the entire study group was divided according to sex. Compared with lean twins, plasma leptin levels were 3.7-fold higher in the obese twins who had visceral fat accumulation greater than the median and 2.1-fold higher in the obese twins who had visceral fat accumulation less than the median. The intrapair differences in leptin levels correlated with the corresponding differences in percentage of body fat in women (r = 0.73; P = 0.003) but not in men and correlated with differences in visceral fat area in men (r = 0.79; P = 0.019) and women (r = 0.73; P = 0.007). In multiple regression analyses that included intrapair differences in visceral fat area and total body fat, the association between differences in visceral fat area and leptin levels was significant in men (P = 0.029) but not in women.
Plasma leptin levels are increased in obese persons, independent of genetic background. Visceral fat may be of special importance in the regulation of leptin levels, but it is probably less important in women than in men.
瘦素是最近发现的一种饱腹感激素,其血浆水平与人类肥胖程度相关。
确定遗传因素或体脂分布是否会影响瘦素水平与肥胖之间的关联。
23对健康的同卵双胞胎(9对男性双胞胎和14对女性双胞胎,年龄在33至59岁之间),他们在肥胖方面存在差异(平均体重差异为18千克)。
采用放射免疫分析法测定空腹血浆瘦素水平。通过磁共振成像估计腹部脂肪在内脏和皮下组织中的分布情况。
肥胖双胞胎的血浆瘦素水平比瘦双胞胎高3倍(均值±标准差,分别为18.7±12.5微克/升和6.4±4.8微克/升;P<0.001);按性别对整个研究组进行划分时,也观察到了类似差异。与瘦双胞胎相比,内脏脂肪蓄积量大于中位数的肥胖双胞胎血浆瘦素水平高3.7倍,内脏脂肪蓄积量小于中位数的肥胖双胞胎血浆瘦素水平高2.1倍。瘦素水平的双胞胎内差异与女性体脂百分比的相应差异相关(r=0.73;P=0.003),但与男性无关,且与男性(r=0.79;P=0.019)和女性(r=0.73;P=0.007)的内脏脂肪面积差异相关。在包含内脏脂肪面积和全身脂肪双胞胎内差异的多元回归分析中,内脏脂肪面积差异与瘦素水平之间的关联在男性中显著(P=0.029),但在女性中不显著。
肥胖者血浆瘦素水平升高,与遗传背景无关。内脏脂肪在瘦素水平调节中可能具有特殊重要性,但在女性中可能不如在男性中重要。