Thyroid function, pernicious anemia and erythropoiesis: a two-sample Mendelian randomization study. Issue 15 (28th February 2022)

• Record Type: Journal Article
• Authors: Kjaergaard, Alisa D; Teumer, Alexander; Marouli, Eirini; Deloukas, Panos; Kuś, Aleksander; Sterenborg, Rosalie; Åsvold, Bjørn O; Medici, Marco; Ellervik, Christina
• Is Part Of: Human molecular genetics. Volume 31:Issue 15(2022)
• Page Start: 2548
• Page End: 2559
• Publication Date: 2022-02-28
• Subjects: Human molecular genetics -- Periodicals; Human chromosome abnormalities -- Periodicals; 572.8
• DOI: 10.1093/hmg/ddac052
• Languages: English
• ISSNs: 0964-6906

Abstract

Abstract: Autoimmune thyroid disease (AITD) and pernicious anemia (PA) often coexist, but the directionality is unknown. In a two-sample Mendelian randomization (MR) analysis, using summary statistics from large genome-wide association studies (GWASs) in Europeans ( N = 49 269–755 406), we examined the genetic associations between thyroid function, PA and markers of erythropoiesis. We performed inverse variance weighted random-effects MR, several sensitivity MR analyses, and bidirectional MR and MR Steiger for directionality. AITD and PA were associated bidirectionally ( P ≤ 8 × 10 −6 ). Neither euthyroid thyroid stimulating hormone (TSH) nor free thyroxine (FT4) were causally associated with PA. One standard deviation (SD) increase in euthyroid FT4 regulated by genetic variants in deiodinases 1 and 2 genes ( DIO1/DIO2 ), corresponding to low-normal free triiodothyronine (FT3) levels, was causally associated with a pernicious/macrocytic anemia pattern, i.e. decreased erythrocyte counts (rank-based inverse normal transformed β = −0, 064 [95% confidence interval: −0, 085, −0, 044], P = 8 × 10 −10 ) and hemoglobin (−0.028 [−0.051, −0.005], P = 0.02) and increased mean corpuscular hemoglobin (0.058 [0.025, 0.091], P = 5 × 10 −4 ) and mean corpuscular volume levels (0.075 [0.052, 0.098], P = 1 × 10 −8 ). Meanwhile, subclinical hyperthyroidism mirrored that pattern. AITD was causally associated with increased erythrocyte distribution width ( P = 0.007) and decreased reticulocyte counts ( P ≤ 0.02), whereas high-normal FT4 regulated by DIO1/DIO2 variants was causally associated with decreased bilirubin (−0.039 (−0.064, −0.013), P = 0.003). In conclusion, the bidirectional association between AITD and PA suggests a shared heritability for these two autoimmune diseases. AITD was causally associated with impaired erythropoiesis and not autoimmune hemolysis. Additionally, in euthyroid individuals, local regulation of thyroid hormones by deiodinases likely plays a role in erythropoiesis.