IGF1, insulin like growth factor 1, 3479

N. diseases: 1206; N. variants: 36
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0001206
Disease: Acromegaly
Acromegaly
0.400 AlteredExpression disease BEFREE MN frequency in the lymphocytes of patients with acromegaly increased with elevated serum IGF-1 levels (p<0.05), whereas the number of NPBs and the frequency of apoptotic cells decreased with elevated serum IGF-1 levels (p<0.01 and p<0.05 respectively). 24382376 2014
CUI: C0001206
Disease: Acromegaly
Acromegaly
0.400 AlteredExpression disease BEFREE This lack of association may suggest that tear IGF-1 levels might not have an effect on CCT or IOP findings in patients with acromegaly. 28127733 2017
CUI: C0001206
Disease: Acromegaly
Acromegaly
0.400 Biomarker disease BEFREE Acromegaly is a disease of exaggerated somatic growth and distorted proportion arising from hypersecretion of growth hormone (GH) and insulin-like growth factor 1 (IGF-1). 20234189 2010
CUI: C0001206
Disease: Acromegaly
Acromegaly
0.400 AlteredExpression disease BEFREE Cabergoline monotherapy is reported to normalize IGF-I levels in more than one-third of patients with acromegaly. 28025719 2017
CUI: C0001206
Disease: Acromegaly
Acromegaly
0.400 AlteredExpression disease BEFREE The paradoxical GH response reflected the clinical characteristics, especially IGF-I level, glucose metabolism, and drug efficacy in acromegaly. 30476255 2019
CUI: C0001206
Disease: Acromegaly
Acromegaly
0.400 AlteredExpression disease BEFREE While current treatment modalities have greatly improved prognoses for most patients, a significant number present clinical symptoms of acromegaly with elevated levels of IGF-1 in the absence of increased GH levels, a phenomenon known as micromegaly. 31071497 2020
CUI: C0001206
Disease: Acromegaly
Acromegaly
0.400 Biomarker disease BEFREE Control of acromegaly was defined as a random serum growth hormone (GH) < 1 ng/mL and an age-normalised serum insulin-like growth factor-I (IGF-I) value. 28879646 2017
CUI: C0001206
Disease: Acromegaly
Acromegaly
0.400 AlteredExpression disease BEFREE <b>Purpose:</b> Excess growth hormone (GH) secretion in acromegaly patients results in increased levels of IGF-1 expression, which causes the clinical manifestations of acromegaly. 30619084 2018
CUI: C0001206
Disease: Acromegaly
Acromegaly
0.400 GeneticVariation disease BEFREE One hundred acromegaly patients on medical therapy (mean age = 47.1 years; SD = 11.96) completed an online preference study evaluating hypothetical patient profiles described in terms of insulin-like growth factor-I (IGF-I) levels, tumor size, comorbid conditions, signs/symptoms, and quality of life (QoL). 30627944 2019
CUI: C0001206
Disease: Acromegaly
Acromegaly
0.400 Biomarker disease BEFREE Background Biochemical control of GH/IGF-I excess in acromegaly (ACRO) is associated with persistent impairment of trabecular microstructure leading to increased risk of vertebral fractures. 30640713 2019
CUI: C0001206
Disease: Acromegaly
Acromegaly
0.400 AlteredExpression disease BEFREE Although the normalisation of GH and IGF1 levels is the main objective in all patients with acromegaly, GH and IGF1 levels may be discordant, especially during somatostatin analogue therapy. 24144967 2014
CUI: C0001206
Disease: Acromegaly
Acromegaly
0.400 GeneticVariation disease BEFREE An uncontrolled hyperactive GH-IGF-1 axis may play a dominant role in the development of PTC rather than the BRAFV600E mutation in patients with acromegaly. 25329702 2014
CUI: C0001206
Disease: Acromegaly
Acromegaly
0.400 AlteredExpression disease BEFREE A phase III trial of oral octreotide capsules demonstrated that this treatment can safely sustain suppressed levels of GH and IGF-1 and reduce the severity of symptoms in patients with acromegaly previously controlled by injectable SRL therapy, with the added benefit of no injection-site reactions. 26610414 2016
CUI: C0001206
Disease: Acromegaly
Acromegaly
0.400 AlteredExpression disease BEFREE Our data indicates that tissue-level properties of cortical bone are significantly altered in patients with controlled acromegaly after reversal of long-term exposure to pathologically high GH and IGF-1 levels. 28077497 2017
CUI: C0001206
Disease: Acromegaly
Acromegaly
0.400 Biomarker disease BEFREE GH, IGF-1, and Age Are Important Contributors to Thyroid Abnormalities in Patients with Acromegaly. 29593792 2018
CUI: C0001206
Disease: Acromegaly
Acromegaly
0.400 Biomarker disease BEFREE Management of acromegaly is particularly challenging in cases where discordant information is obtained from measurement of GH concentrations following oral glucose load and from measurement of IGF-I. 28168377 2017
CUI: C0001206
Disease: Acromegaly
Acromegaly
0.400 Biomarker disease BEFREE A univariate analysis was conducted and eight features, including age, hypertension, ophthalmic disorders, GH, IGF-1, nadir GH, maximal tumor diameter, and Knosp grade, were significantly associated with the TSS response in patients with acromegaly. 31673954 2020
CUI: C0001206
Disease: Acromegaly
Acromegaly
0.400 Biomarker disease BEFREE Included in this prospective cohort were 41 patients with acromegaly who underwent surgery alone and achieved postoperative normalization of insulin-like growth factor-1. 27681883 2017
CUI: C0001206
Disease: Acromegaly
Acromegaly
0.400 Biomarker disease BEFREE Recently, a GH-receptor blocking agent, pegvisomant, was licensed for use in acromegaly and appears to normalise IGF-1 in almost all patients. 16262568 2005
CUI: C0001206
Disease: Acromegaly
Acromegaly
0.400 GeneticVariation disease BEFREE Therefore, routine screening of GD should be considered in women with acromegaly, particularly in those with risk factors for GD and with uncontrolled IGF-1 levels before pregnancy. 31520541 2019
CUI: C0001206
Disease: Acromegaly
Acromegaly
0.400 Biomarker disease BEFREE Significant correlation could be detected between insulin-like growth factor 1 (IGF-1) index and peak superior LA-CS (r = .49, P = .05) in acromegaly. 29569265 2018
CUI: C0001206
Disease: Acromegaly
Acromegaly
0.400 Biomarker disease BEFREE Acromegaly is characterized by an excess of growth hormone (GH) and insulin like growth-factor 1 (IGF1). 31751301 2019
CUI: C0001206
Disease: Acromegaly
Acromegaly
0.400 Biomarker disease BEFREE 530 patients (36%) reported at least 1 acral enlargement symptom and were tested for IGF-1, 41 were above range, persisted in 7, and among those, 2 cases of acromegaly were diagnosed (prevalence of at least 1.35 cases/1000). 28898247 2017
CUI: C0001206
Disease: Acromegaly
Acromegaly
0.400 AlteredExpression disease BEFREE To evaluate the response of bone to chronic long-term growth hormone (GH) and insulin-like growth factor-1 (IGF1) excess by measuring the expression of selected mRNA and microRNA (miR) in bone tissue samples of patients with active acromegaly. 29374071 2018
CUI: C0001206
Disease: Acromegaly
Acromegaly
0.400 Biomarker disease BEFREE A low secretory activity of these tumours might explain the normal plasma values for GH and insulin-like growth factor 1 (IGF1) and the absence of clinical signs of acromegaly. 27913611 2017