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英国生物库队列中白细胞亚型和肥胖与皮肤恶性黑色素瘤发病风险的前瞻性关联。

Prospective associations of leucocyte subtypes and obesity with the risk of developing cutaneous malignant melanoma in the UK Biobank cohort.

机构信息

Department of Epidemiology and Biostatistics, School of Public Health, Imperial College London, White City Campus, 90 Wood Lane, London, W12 0BZ, UK.

Department of Inflammation Biology, School of Immunology and Microbial Sciences, King's College London, London, UK.

出版信息

BMC Cancer. 2024 May 23;24(1):625. doi: 10.1186/s12885-024-12344-0.

Abstract

BACKGROUND

Obesity is associated with chronic low-grade inflammation, which is linked to cancer development. Abdominal obesity (a body mass index, ABSI), however, has unusually been associated inversely with cutaneous malignant melanoma (CMM), while general obesity (body mass index, BMI) is associated positively. Leucocytes participate in inflammation and are higher in obesity, but prospective associations of leucocytes with cutaneous malignant melanoma are unclear.

METHODS

We examined the prospective associations of neutrophil, lymphocyte, and monocyte counts (each individually), as well as the prospective associations of ABSI and BMI, with cutaneous malignant melanoma in UK Biobank. We used multivariable Cox proportional hazards models and explored heterogeneity according to sex, menopausal status, age (≥ 50 years at recruitment), smoking status, ABSI (dichotomised at the median: ≥73.5 women; ≥79.8 men), BMI (normal weight, overweight, obese), and time to diagnosis.

RESULTS

During a mean follow-up of 10.2 years, 2174 CMM cases were ascertained in 398,450 participants. There was little evidence for associations with neutrophil or lymphocyte counts. Monocyte count, however, was associated inversely in participants overall (HR = 0.928; 95%CI: 0.888-0.971; per one standard deviation increase; SD = 0.14410/L women; SD = 0.16910/L men), specifically in older participants (HR = 0.906; 95%CI: 0.862-0.951), and more clearly in participants with low ABSI (HR = 0.880; 95%CI: 0.824-0.939), or with BMI ≥ 25 kg/m (HR = 0.895; 95%CI: 0.837-0.958 for overweight; HR = 0.923; 95%CI: 0.848-1.005 for obese). ABSI was associated inversely in pre-menopausal women (HR = 0.810; 95%CI: 0.702-0.935; SD = 4.95) and men (HR = 0.925; 95%CI: 0.867-0.986; SD = 4.11). BMI was associated positively in men (HR = 1.148; 95%CI: 1.078-1.222; SD = 4.04 kg/m). There was little evidence for heterogeneity according to smoking status. The associations with monocyte count and BMI were retained to at least 8 years prior to diagnosis, but the association with ABSI was observed up to 4 years prior to diagnosis and not for longer follow-up time.

CONCLUSIONS

Monocyte count is associated prospectively inversely with the risk of developing CMM in older individuals, while BMI is associated positively in men, suggesting a mechanistic involvement of factors related to monocytes and subcutaneous adipose tissue in melanoma development. An inverse association with ABSI closer to diagnosis may reflect reverse causality or glucocorticoid resistance.

摘要

背景

肥胖与慢性低度炎症有关,而慢性低度炎症与癌症的发生有关。然而,腹部肥胖(身体质量指数,ABSI)与皮肤恶性黑色素瘤(CMM)呈负相关,而一般肥胖(体重指数,BMI)与 CMM 呈正相关。白细胞参与炎症反应,在肥胖症中更高,但白细胞与皮肤恶性黑色素瘤的前瞻性关联尚不清楚。

方法

我们在英国生物银行中研究了中性粒细胞、淋巴细胞和单核细胞计数(单独研究),以及 ABSI 和 BMI 与皮肤恶性黑色素瘤的前瞻性关联。我们使用多变量 Cox 比例风险模型,并根据性别、绝经状态、年龄(招募时≥50 岁)、吸烟状况、ABSI(中位数二分位数:女性≥73.5;男性≥79.8)、BMI(正常体重、超重、肥胖)和诊断前时间进行异质性探索。

结果

在平均 10.2 年的随访期间,在 398450 名参与者中确定了 2174 例 CMM 病例。中性粒细胞或淋巴细胞计数与 CMM 之间几乎没有关联。然而,单核细胞计数在所有参与者中呈负相关(HR=0.928;95%CI:0.888-0.971;每增加一个标准偏差;女性的 SD=0.14410/L;男性的 SD=0.16910/L),特别是在年龄较大的参与者中(HR=0.906;95%CI:0.862-0.951),在 ABSI 较低的参与者中更为明显(HR=0.880;95%CI:0.824-0.939),或 BMI≥25 kg/m(超重的 HR=0.895;95%CI:0.837-0.958;肥胖的 HR=0.923;95%CI:0.848-1.005)。在绝经前女性(HR=0.810;95%CI:0.702-0.935;SD=4.95)和男性(HR=0.925;95%CI:0.867-0.986;SD=4.11)中,ABSI 呈负相关。BMI 在男性中呈正相关(HR=1.148;95%CI:1.078-1.222;SD=4.04 kg/m)。根据吸烟状况,几乎没有证据表明存在异质性。单核细胞计数和 BMI 与 CMM 风险之间的关联至少在诊断前 8 年就存在,但与 ABSI 的关联在诊断前 4 年就存在,而不是更长的随访时间。

结论

在年龄较大的个体中,单核细胞计数与 CMM 的发病风险呈负相关,而 BMI 与男性呈正相关,这表明与单核细胞和皮下脂肪组织相关的因素可能参与了黑色素瘤的发生。ABSI 与诊断更接近的负相关可能反映了反向因果关系或糖皮质激素抵抗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2983/11112846/956d1886725e/12885_2024_12344_Fig1_HTML.jpg

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