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Biomarkers for Monitoring of Changes in Disease Activity in Ulcerative Colitis.
Tatsumi, Yoshihiro; Kakimoto, Kazuki; Hara, Azusa; Mizuta, Noboru; Numa, Keijiro; Kinoshita, Naohiko; Nakazawa, Kei; Koshiba, Ryoji; Hirata, Yuki; Ota, Kazuhiro; Miyazaki, Takako; Nakamura, Shiro; Sakagami, Kayoko; Arimitsu, Shoko; Ito, Hiroaki; Nishikawa, Hiroki.
Afiliación
  • Tatsumi Y; 2nd Department of Internal Medicine, Osaka Medical and Pharmaceutical University, Takatsuki City 569-8686, Japan.
  • Kakimoto K; 2nd Department of Internal Medicine, Osaka Medical and Pharmaceutical University, Takatsuki City 569-8686, Japan.
  • Hara A; Kinshukai Infusion Clinic, Osaka-shi 530-0011, Japan.
  • Mizuta N; 2nd Department of Internal Medicine, Osaka Medical and Pharmaceutical University, Takatsuki City 569-8686, Japan.
  • Numa K; Kinshukai Infusion Clinic, Osaka-shi 530-0011, Japan.
  • Kinoshita N; 2nd Department of Internal Medicine, Osaka Medical and Pharmaceutical University, Takatsuki City 569-8686, Japan.
  • Nakazawa K; 2nd Department of Internal Medicine, Osaka Medical and Pharmaceutical University, Takatsuki City 569-8686, Japan.
  • Koshiba R; 2nd Department of Internal Medicine, Osaka Medical and Pharmaceutical University, Takatsuki City 569-8686, Japan.
  • Hirata Y; 2nd Department of Internal Medicine, Osaka Medical and Pharmaceutical University, Takatsuki City 569-8686, Japan.
  • Ota K; 2nd Department of Internal Medicine, Osaka Medical and Pharmaceutical University, Takatsuki City 569-8686, Japan.
  • Miyazaki T; 2nd Department of Internal Medicine, Osaka Medical and Pharmaceutical University, Takatsuki City 569-8686, Japan.
  • Nakamura S; Kinshukai Infusion Clinic, Osaka-shi 530-0011, Japan.
  • Sakagami K; 2nd Department of Internal Medicine, Osaka Medical and Pharmaceutical University, Takatsuki City 569-8686, Japan.
  • Arimitsu S; 2nd Department of Internal Medicine, Osaka Medical and Pharmaceutical University, Takatsuki City 569-8686, Japan.
  • Ito H; Kinshukai Infusion Clinic, Osaka-shi 530-0011, Japan.
  • Nishikawa H; 2nd Department of Internal Medicine, Osaka Medical and Pharmaceutical University, Takatsuki City 569-8686, Japan.
J Clin Med ; 12(22)2023 Nov 18.
Article en En | MEDLINE | ID: mdl-38002777
ABSTRACT

BACKGROUND:

In recent years, various biomarkers of ulcerative colitis (UC) have emerged; however, few studies have simultaneously examined the utility of multiple biomarkers for monitoring disease activity. Additionally, serum leucine-rich alpha-2 glycoprotein (LRG), a new biomarker, may show a blunt response to anti-TNF antibody therapy. This prospective study explored effective biomarkers that could monitor disease activity changes in patients with UC. In addition, we examined the effect of anti-TNF antibody therapy on changes in LRG.

METHODS:

Blood and stool samples were collected twice from patients with UC at baseline and at least 8 weeks later. Changes in serum LRG, interleukin (IL)-6, prealbumin (pre-Alb), high-sensitivity C-reactive protein (hs-CRP), CRP, and fecal calprotectin (FC) were measured and correlated with changes in disease activity. The relationship between anti-TNF antibody therapy and LRG levels was also examined in patients with the same disease activity.

RESULTS:

Forty-eight patients with UC (96 samples) were analyzed. ΔLRG and ΔIL-6 correlated strongly with the change in the partial Mayo (pMayo) score between the two time points (ΔpMayo) (r = 0.686, 0.635, respectively). In contrast, FC and IL-6 were particularly accurate predictors of clinical remission, and their area under the curves (AUCs) were significantly higher than that of CRP (AUC 0.81, 0.76 vs. 0.50; p = 0.001, 0.005). No association was found between the administration of anti-TNF antibody preparations and the LRG values.

CONCLUSIONS:

Correlations were found between changes in UC disease activity and LRG, IL-6, pre-Alb, hs-CRP, CRP, and FC. LRG reflects disease activity during anti-TNF antibody therapy.
Palabras clave

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: J Clin Med Año: 2023 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: J Clin Med Año: 2023 Tipo del documento: Article