Karadeniz Yusuf, Karakose Melia
Department of Internal Medicine, Division of Endocrinology and Metabolism, Karaman Training and Research Hospital, Karaman 70200, Türkiye.
Department of Internal Medicine, Division of Endocrinology and Metabolism, Faculty of Medicine, Necmettin Erbakan University, Konya 42090, Türkiye.
J Clin Med. 2025 Jul 8;14(14):4822. doi: 10.3390/jcm14144822.
: Acromegaly is associated with multiple metabolic comorbidities, but the relationship between disease activity and metabolic dysfunction-associated steatotic liver disease (MASLD) or cardiovascular risk remains unclear. This study aimed to assess the prevalence and severity of MASLD and liver fibrosis in patients with acromegaly relative to healthy controls and explore whether disease activity influences these parameters. We also evaluated cardiovascular risk indicators in acromegaly patients. : A retrospective case-control study was conducted between 2000 and 2022, involving 58 acromegaly patients and 58 healthy controls. Patients were classified as active or in biochemical remission. MASLD was assessed using the fibrosis-4 (FIB-4) index, MASLD fibrosis score, body mass index, diabetes (BARD) score, the aspartate aminotransferase-to-platelet index (APRI), and the aspartate aminotransferase-to-alanine aminotransferase ratio. Cardiovascular evaluation included pulse wave velocity (PWV) and carotid intima-media thickness (CIMT). : The median age of the acromegaly group was 47.5 (39-57) years, compared to 42 (40-48) years in the control group ( = 0.041). APRI ( < 0.001), FIB-4 ( < 0.001), MASLD fibrosis score ( < 0.001), and BARD score ( < 0.001) were significantly higher in the acromegaly group. The prevalence of hepatic steatosis was also higher in the acromegaly group ( < 0.001). Diastolic blood pressure ( = 0.015) and PWV ( = 0.012) were significantly higher in the acromegaly group. : Acromegaly patients have an increased risk of MASLD and fibrosis, but this risk is unassociated with disease activity. Similarly, cardiovascular risk parameters remain elevated regardless of disease activity. These findings suggest that the systemic effects of acromegaly may persist despite biochemical control.
肢端肥大症与多种代谢合并症相关,但疾病活动与代谢功能障碍相关脂肪性肝病(MASLD)或心血管风险之间的关系仍不清楚。本研究旨在评估肢端肥大症患者相对于健康对照者MASLD和肝纤维化的患病率及严重程度,并探讨疾病活动是否会影响这些参数。我们还评估了肢端肥大症患者的心血管风险指标。:在2000年至2022年期间进行了一项回顾性病例对照研究,纳入58例肢端肥大症患者和58例健康对照者。患者被分为疾病活动期或生化缓解期。使用纤维化-4(FIB-4)指数、MASLD纤维化评分、体重指数、糖尿病(BARD)评分、天冬氨酸转氨酶与血小板比值指数(APRI)以及天冬氨酸转氨酶与丙氨酸转氨酶比值评估MASLD。心血管评估包括脉搏波速度(PWV)和颈动脉内膜中层厚度(CIMT)。:肢端肥大症组的中位年龄为47.5(39 - 57)岁,而对照组为42(40 - 48)岁(P = 0.041)。肢端肥大症组的APRI(P < 0.001)、FIB-4(P < 0.001)、MASLD纤维化评分(P < 0.001)和BARD评分(P < 0.001)显著更高。肢端肥大症组肝脂肪变性的患病率也更高(P < 0.001)。肢端肥大症组的舒张压(P = 0.015)和PWV(P = 0.012)显著更高。:肢端肥大症患者发生MASLD和纤维化的风险增加,但这种风险与疾病活动无关。同样,无论疾病活动如何,心血管风险参数仍会升高。这些发现表明,尽管生化指标得到控制,肢端肥大症的全身影响可能仍然存在。