goiter: pathophysiology and clinical aspects

55
Goiter: Pathophysiology and clinical aspects Joaquín Lado Abeal, MD, PhD Department of Internal Medicine TTUHSC-SOM, Lubbock

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Goiter: Pathophysiology and clinical aspects. Joaquín Lado Abeal, MD, PhD. Department of Internal Medicine TTUHSC-SOM, Lubbock. Iodine intake (goitrogens). Gender. Genetic. From Iodine Satus Worldwide. WHO Global Data Base on Iodine Deficiency. 2004. - PowerPoint PPT Presentation

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Page 1: Goiter: Pathophysiology and clinical aspects

Goiter: Pathophysiology

and clinical aspects

Joaquín Lado Abeal, MD, PhD

Department of Internal Medicine

TTUHSC-SOM, Lubbock

Page 2: Goiter: Pathophysiology and clinical aspects

Iodine intake

(goitrogens)

Gender

Genetic

Page 3: Goiter: Pathophysiology and clinical aspects

From Iodine Satus Worldwide. WHO Global Data Base on Iodine Deficiency. 2004

Page 4: Goiter: Pathophysiology and clinical aspects

From Iodine Satus Worldwide. WHO Global Data Base on Iodine Deficiency. 2004

Page 5: Goiter: Pathophysiology and clinical aspects

San Bartolomeu da Mota (A Mota, Arzua, Galicia)

Page 6: Goiter: Pathophysiology and clinical aspects
Page 7: Goiter: Pathophysiology and clinical aspects

Dr Gregorio Maranon

Page 8: Goiter: Pathophysiology and clinical aspects

CRETINISM

Neurological Myxedematose

Page 9: Goiter: Pathophysiology and clinical aspects
Page 10: Goiter: Pathophysiology and clinical aspects
Page 11: Goiter: Pathophysiology and clinical aspects
Page 12: Goiter: Pathophysiology and clinical aspects
Page 13: Goiter: Pathophysiology and clinical aspects

T3T4

TSH

Hyperthyrodism

High T4/T3Low TSH

Hypothyrodism

Low T4/T3High TSH

Page 14: Goiter: Pathophysiology and clinical aspects

Thyroid Hormone Synthesis

Page 15: Goiter: Pathophysiology and clinical aspects

TSH

Diferentiation Proliferation

Insulin/IGF-I

Page 16: Goiter: Pathophysiology and clinical aspects

Pituitary TSHoma

TSH

Page 17: Goiter: Pathophysiology and clinical aspects

Graves-Basedow disease

Page 18: Goiter: Pathophysiology and clinical aspects

TSHR mutations

Page 19: Goiter: Pathophysiology and clinical aspects

November 2001

May 2003

Syndrome of Resistance to Thyroid Hormone Action (SRTH)T

SH

(m

U/L

)

Number of days

0

50

100

150

200

250

TG

g/L

)6005004003002001000

0

5

10

15

150 200 250L-T3 dose µg c.2.d.

31

32

33

34

35

36

37

6005004003002001000

30

Ne

ck

dia

me

ter

(c

m)

49

4547

51

We

igh

t (K

g)

TT

4 (

µg

/dl)

0.1

1

2

0.05

0.5

Page 20: Goiter: Pathophysiology and clinical aspects

N Range Mean SE p p

Euthyroid (Buenos Aires) 20 2.4-3.6 3.2 0.4

Non goiter (Neuquen) 14 2.4-5.6 4 0.8 <0.01

Goiter, grade I & II 6 3.2-5.6 3.6 0.8 NS NS

Goiter, grade III 8 2.4-5.6 4 0.8 <0.05 NS

Goiter, grado I & II 7 2.4-4.8 4 0.8 <0.05 NS

Goiter, grado III 5 2.8-7.2 4 0.8 <0.05 NS

TSH (µU/ml)

MA Pisarev, RD Utiger, JP Salvaneschi, N Altschuler, LJ DeGroot. Serum TSH and thyroxine in Goitrous Subjects in Argentina. J Clin Endocr. 30:680-681. 1970.

Page 21: Goiter: Pathophysiology and clinical aspects

28.1.04 11.4.05 30.8.05

TSH µU/ml 0.42 0.10 0.08

FT4 ng/dl 1.08 0.88 0.80

FT3 pg/ml 3.29 3.89 3.65

NORMAL

0.35-5.50

0.85-1.86

2.20-4.70

MULTINODULAR GOITER

Ab TPO

AbTG

< 33

< 100

Page 22: Goiter: Pathophysiology and clinical aspects

Pendred Sydrome

Page 23: Goiter: Pathophysiology and clinical aspects

50 µg/day T4 (starting March 04)

100 µg/day T4 (starting Nov 04)

100 µg/day T4 Post surgery

(starting February 05)

Total Thyroidectomy(February 05)

27.11.03 28.05.04 2.02.05 4.03.05 Rango

Normal

TSH, µUI/ml

FT4, ng/dl

FT3, pg/ml

Tg

Anti-TPO Ab

Anti-TG Ab

IGF-1, ng/ml

Yoduria µg/L

3.29

0.51

3.78

153

1.99

0.77

1312

<10

<20

0.12

0.91

3.36

100

102

6.39

1.25

0.35-5.50

0.85-1.86

2.20-4.70

<35

<40

81-267

25-450

Page 24: Goiter: Pathophysiology and clinical aspects

T4

rT3

T3

T4

D1, D2

D3

T4

T3

Page 25: Goiter: Pathophysiology and clinical aspects

p.R277X / c.6205+1delG

WT/p.R277X

R277X

Red=goiterc.6205+1delG

WT/c.6205+1delG

WT / WT WT/c.6205+1delG

p.R277X / c.6205+1delG

p.R277X / c.6205+1delG

p.R277X / c.6205+1delG

T GTAAGTTCATTGTAAGTTCATTG

wildtypemutant

c.886C>Tp.R277X

c.6205+1delGExon 35 skipping

T

Exon 35 Intron 35

THYROGLOBULIN GENE MUTATIONS

Exon 7

WT/c.6205+1delG

Page 26: Goiter: Pathophysiology and clinical aspects
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Exon 34 Exon 36

Exon 35 skipping

K P M S L

TT GCT CAA AAT AAT GCT CCC AGT TTT TGC CCT TTG GTT GTT CTG CCT TCC CTC ACA GAG AAG I A Q N N A P S F C P L V V L P S L T E K

Page 29: Goiter: Pathophysiology and clinical aspects

p.R277X /c.6205+1delG WT /c.6205+1delG

Page 30: Goiter: Pathophysiology and clinical aspects
Page 31: Goiter: Pathophysiology and clinical aspects
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Thyroglobulin mutations

Goiter

defective hormone synthesis

high serum TSH

unfolded protein response

apoptosis

p53, NF-kB, MPAKs, VEGF

Cancer

BRAF mutations

oxidative stress

Page 33: Goiter: Pathophysiology and clinical aspects

Afrikaner cow

1 48

9

TG

Page 34: Goiter: Pathophysiology and clinical aspects
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INACTIVE

GDP

ACTIVE

GTP

GEF

GTPGDPGAP

Pi

RAS

Page 37: Goiter: Pathophysiology and clinical aspects

R Wetzker, Frank-D Bohmer. Transactivation joins multiple tracks to the ERK/MAPK Cascade. Nature Reviews. Molecular Biology. 4: 651-657. 2003.

PLCDAG

PKC

Page 38: Goiter: Pathophysiology and clinical aspects

RAS GTP

RalGDS Raf PLC PI3K

Ral

ProliferationCell survival

MEK

ERK

Proliferation

AKT/PKB

Growth, cell survivalH2O2

Ca 2+ intracelular

H2O2

Transcription

Page 39: Goiter: Pathophysiology and clinical aspects

0%

5%

10%

15%

20%

25%

30%

Colloid nodules

Follicular adenomas

Papilary carcinomas

Follicular carcinomas

H1-RAS(12/13)

H2-RAS(61)

K1-RAS(12/13)

K2-RAS(61)

N1-RAS(12/13)

N2-RAS(61)

V. Vasko et al. JCEM. 88(6):2745-2752. 2003

RAS Mutations in Thyroid Tumors

Page 40: Goiter: Pathophysiology and clinical aspects

TTF-1

PAX-8

Tg

Normal Human Thyrocites

H-RAS (V-12)CONTROL

4 Days 3 Weeks 3 Weeks

V Gire, D Wynford-Thomas. Oncogene. 19:737-744.2000

Page 41: Goiter: Pathophysiology and clinical aspects

RAS

MAPKPI3K RalGEF

CELL SURVIVAL

PROLIFERATION

GROWTH

Page 42: Goiter: Pathophysiology and clinical aspects

t(2;3)(q13;p25) & -20

AR Marques et al. JCEM. 87(8): 3947-3952. 2002

Chromosomalimbalance

15q loss

Page 43: Goiter: Pathophysiology and clinical aspects

t(2;3)(q13;p25)

TG Kroll et al. Science. 289:1357-1360. 2000Placzkowski KA et al. PPAR Research. 2008

PAX8-PPARG

Page 44: Goiter: Pathophysiology and clinical aspects
Page 45: Goiter: Pathophysiology and clinical aspects

PPAR 1

(exon 1)

A PAX8

(exon 8)

PPAR 1

(exon 1)

B PAX8

(exon 10)

PAX8

(exon 10)

PAX8

(exon 8)

Page 47: Goiter: Pathophysiology and clinical aspects
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66 XXX

From T Dettori et al. Genes, Chromosomes & Cancer. 38: 22-31. 2003.

Aneuploidy (33% Goiters)

Page 50: Goiter: Pathophysiology and clinical aspects

M Iliszko et al. Cancer Genetic and Cytogenetcis. 161: 178-180. 2005

Page 51: Goiter: Pathophysiology and clinical aspects

Cowden Syndrome

Page 52: Goiter: Pathophysiology and clinical aspects

PI3K

I Vivanco, CL Sawyers. Nature Reviews. 2: 489-501.2002

PI3K/AKT Pathway(cell proliferation and survival)

PIK3CA

PTEN=Phosphatase and Tensin

Homolog

Page 53: Goiter: Pathophysiology and clinical aspects

Wang Y et al. JCEM. 92:2387-2390. 2007

Page 54: Goiter: Pathophysiology and clinical aspects

RAS +

PI3K/Akt +

FollicularAdenoma

TSHR +/GNAS +

Follicular Carcinoma

PAX8-PPARG +

PI3K/Akt +++

PAX8-PPARG +

Hurthle Cell Adenoma

Hurthle Cell Carcinoma

GRIM-19 +(gene associated with retinoid-interferon-induced mortality-19)

mtDNA CD +(mtDNA common deletion)

PAX8-PPARG +

Page 55: Goiter: Pathophysiology and clinical aspects

Santiago de Compostela Cathedral