Association of Renal Function and Statin Therapy with Lipoprotein(a) in Patients with Type 2 Diabetes

被引:1
作者
Hiraishi, Chika [1 ,2 ]
Matsui, Sadako [3 ]
Kojima, Takai [4 ]
Sato, Ryo [4 ]
Ando, Kiyotaka [5 ]
Fujimoto, Kei [6 ]
Yoshida, Hiroshi [1 ,2 ,4 ]
机构
[1] Jikei Univ, Grad Sch Med, Sect Internal Med Metab & Nutr, Tokyo, Japan
[2] Jikei Univ, Kashiwa Hosp, Dept Gen Med, 163-1 Kashiwashita, Kashiwa, Chiba 2778567, Japan
[3] Japan Womens Univ, Fac Human Sci & Design, Food & Nutr, Tokyo, Japan
[4] Jikei Univ, Kashiwa Hosp, Dept Lab Med, Kashiwa, Chiba, Japan
[5] Jikei Univ, Kashiwa Hosp, Dept Internal Med, Div Diabet Metab & Endocrinol, Tokyo, Japan
[6] Jikei Univ, Daisan Hosp, Dept Internal Med, Div Diabet Metab & Endocrinol, Tokyo, Japan
关键词
Lipoprotein(a); Type; 2; diabetes; Diabetic kidney disease; Statin; eGFR; CHRONIC KIDNEY-DISEASE; METABOLIC SYNDROME; CARDIOVASCULAR-DISEASE; LDL CHOLESTEROL; RISK; PEOPLE; NEPHROPATHY; PREDICTS; LEVEL;
D O I
10.5551/jat.64261
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Aim: A high level of serum lipoprotein(a) [Lp(a)] is associated with kidney disease development in patients with type 2 diabetes (T2DM). Recent studies have suggested that statins may affect serum levels of Lp(a). However, the statin effect is not well-defined in patients with T2DM with kidney dysfunction. This retrospective study aimed to investigate the relevance of kidney dysfunction and statin therapy to Lp(a) in patients with T2DM. Methods: Japanese patients with T2DM (n=149, 96 men and 53 women) were divided into two groups: statin users (n=79) and non-statin users (n=70). Multiple logistic regression analyses were performed with Lp(a) as the objective variable and estimated glomerular filtration rate (eGFR), hemoglobin A1c, age, gender, and body mass index as the explanatory variables. Results: Lp(a) serum levels were higher in statin users than in non-statin users (P=0.022). Multivariate regression analysis results showed an inverse correlation of eGFR to log Lp(a) in all patients (P=0.009) and in non-statin users (P=0.025), but not in statin users. In a multiple logistic regression analysis for median Lp(a), there was an inverse association between eGFR and Lp(a) level (odds ratio, 0.965; 95% confidence interval, 0.935-0.997; P=0.030) in non-statin users as well as in all participants, but not in statin users. Conclusions: The present study suggests that a high Lp(a) level in patients with T2DM, except in statin users, is significantly associated with decreased eGFR, indicating that the increased Lp(a) levels under statin therapy might diminish the relationship between Lp(a) and eGFR.
引用
收藏
页码:81 / 89
页数:9
相关论文
共 35 条
[1]   Lipoprotein(a) in postmenopausal women: assessment of cardiovascular risk and therapeutic options [J].
Anagnostis, Panagiotis ;
Karras, Spyridon ;
Lambrinoudaki, Irene ;
Stevenson, John C. ;
Goulis, Dimitrios G. .
INTERNATIONAL JOURNAL OF CLINICAL PRACTICE, 2016, 70 (12) :967-977
[2]   Association between lipoprotein(a) level and type 2 diabetes: no evidence for a causal role of lipoprotein(a) and insulin [J].
Buchmann, Nikolaus ;
Scholz, Markus ;
Lill, Christina M. ;
Burkhardt, Ralph ;
Eckardt, Rahel ;
Norman, Kristina ;
Loeffler, Markus ;
Bertram, Lars ;
Thiery, Joachim ;
Steinhagen-Thiessen, Elisabeth ;
Demuth, Ilja .
ACTA DIABETOLOGICA, 2017, 54 (11) :1031-1038
[3]  
Cohen J., 1988, Statistical Power Analysis for the Behavioral Sciences, DOI 10.4324/9780203771587
[4]   Phenotypic Characterization of Genetically Lowered Human Lipoprotein(a) Levels [J].
Emdin, Connor A. ;
Khera, Amit V. ;
Natarajan, Pradeep ;
Klarin, Derek ;
Won, Hong-Hee ;
Peloso, Gina M. ;
Stitziel, Nathan O. ;
Nomura, Akihiro ;
Zekavat, Seyedeh M. ;
Bick, Alexander G. ;
Gupta, Namrata ;
Asselta, Rosanna ;
Duga, Stefano ;
Merlini, Piera Angelica ;
Correa, Adolfo ;
Kessler, Thorsten ;
Wilson, James G. ;
Bown, Matthew J. ;
Hall, Alistair S. ;
Braund, Peter S. ;
Samani, Nilesh J. ;
Schunkert, Heribert ;
Marrugat, Jaume ;
Elosua, Roberto ;
McPherson, Ruth ;
Farrall, Martin ;
Watkins, Hugh ;
Willer, Cristen ;
Abecasis, Goncalo R. ;
Felix, Janine F. ;
Vasan, Ramachandran S. ;
Lander, Eric ;
Rader, Daniel J. ;
Danesh, John ;
Ardissino, Diego ;
Gabriel, Stacey ;
Saleheen, Danish ;
Kathiresan, Sekar .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2016, 68 (25) :2761-2772
[5]  
FRIEDEWALD WT, 1972, CLIN CHEM, V18, P499
[6]   Effect of a multifactorial intervention on mortality in type 2 diabetes [J].
Gaede, Peter ;
Lund-Andersen, Henrik ;
Parving, Hans-Henrik ;
Pedersen, Oluf .
NEW ENGLAND JOURNAL OF MEDICINE, 2008, 358 (06) :580-591
[7]  
Grundy SM, 2019, J AM COLL CARDIOL, V73, P3168, DOI [10.1016/j.jacc.2018.11.002, 10.1161/CIR.0000000000000625, 10.1016/j.jacc.2018.11.003]
[8]   A new Classification of Diabetic Nephropathy 2014: a report from Joint Committee on Diabetic Nephropathy [J].
Haneda, Masakazu ;
Utsunomiya, Kazunori ;
Koya, Daisuke ;
Babazono, Tetsuya ;
Moriya, Tatsumi ;
Makino, Hirofumi ;
Kimura, Kenjiro ;
Suzuki, Yoshiki ;
Wada, Takashi ;
Ogawa, Susumu ;
Inaba, Masaaki ;
Kanno, Yoshihiko ;
Shigematsu, Takashi ;
Masakane, Ikuto ;
Tsuchiya, Ken ;
Honda, Keiko ;
Ichikawa, Kazuko ;
Shide, Kenichiro .
JOURNAL OF DIABETES INVESTIGATION, 2015, 6 (02) :242-246
[9]   The antifibrinolytic effect of lipoprotein(a) in heterozygous subjects is modulated by the relative concentration of each of the apolipoprotein(a) isoforms and their affinity for fibrin [J].
Hervio, L ;
GirardGloba, A ;
Durlach, V ;
AnglesCano, E .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 1996, 26 (05) :411-417
[10]   In vivo kinetic studies to further understand pathogenesis of abnormal lipoprotein metabolism in chronic kidney disease [J].
Ikewaki, Katsunori .
CLINICAL AND EXPERIMENTAL NEPHROLOGY, 2014, 18 (02) :261-264